﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Labslink Research News</title><link>http://www.labslink.com</link><description>The latest research news from labslink.com.</description><copyright>Copyright 2009 Labslink.com. All rights reserved.</copyright><image><url>http://www.labslink.com/images/logo.gif</url><title>Labslink.com</title><link>http://www.labslink.com</link></image><item><title>Making do with more: Joint BioEnergy Institute researchers engineer plant cell walls to boost sugar yields for biofuels</title><description>When blessed with a resource in overwhelming abundance it&amp;rsquo;s generally a  good idea to make valuable use of that resource. Lignocellulosic biomass  is the most abundant organic material on Earth. For thousands of years  it has been used as animal feed, and for the past two centuries has been  a staple of the paper industry. This abundant resource, however, could  also supply the sugars needed to produce advanced biofuels that can  supplement or replace fossil fuels.......&amp;gt;&lt;a href="http://newscenter.lbl.gov/feature-stories/2013/03/29/making-do-with-more-joint-bioenergy-institute-researchers-engineer-plant-cell-walls-to-boost-sugar-yields-for-biofuels/" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9319</link><pubDate>Fri, 29 Mar 2013 19:03:03 PDT</pubDate></item><item><title>Bugs need symbiotic bacteria to exploit plant seeds</title><description>Aggregations of the red and black colored firebugs are ubiquitous under  linden trees in Central Europe, where the bugs can reach astounding  population densities. While these insects have no impact on humans,  their African, Asian, and American relatives, the cotton stainers, are  serious agricultural pests of cotton and other Malvaceous plants.......&amp;gt; &lt;a href="http://www.ice.mpg.de/ext/976.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9077</link><pubDate>Wed, 09 Jan 2013 14:32:12 PDT</pubDate></item><item><title>Invading species can extinguish native plants despite recent reports</title><description>Ecologists at the University of Toronto and the Swiss Federal Institute  of Technology Zurich (ETH Zurich) have found that, given time, invading  exotic plants will likely eliminate native plants growing in the wild  despite recent reports to the contrary........&amp;gt; &lt;a href="http://www.artsci.utoronto.ca/main/media-releases/invading-species-can-extinguish-native-plants-despite-recent-reports" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9075</link><pubDate>Wed, 09 Jan 2013 14:29:16 PDT</pubDate></item><item><title>Increasing drought stress challenges vulnerable hydraulic system of plants, GW professor finds</title><description>The hydraulic system of trees is so finely-tuned that predicted  increases in drought due to climate change may lead to catastrophic  failure in many species. A recent paper co-authored by George Washington  University Assistant Professor of Biological Sciences Amy Zanne finds  that those systems in plants around the globe are operating at the top  of their safety threshold, making forest ecosystems vulnerable to  increasing environmental stress........&amp;gt; &lt;a href="https://mediarelations.gwu.edu/increasing-drought-stress-predicted-challenge-vulnerable-hydraulic-system-plants-george-washington" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8876</link><pubDate>Tue, 27 Nov 2012 14:41:59 PDT</pubDate></item><item><title>Algae can draw energy from other plants</title><description>Until now, it was believed that only worms, bacteria, and fungi could  digest vegetable cellulose and use it as a source of carbon for their  growth and survival. Plants, in contrast, engage in the photosynthesis  of carbon dioxide, water, and light. In a series of experiments,  Professor Dr. Olaf Kruse and his team cultivated the microscopically  small green alga species Chlamydomonas........&amp;gt;&lt;a href="http://ekvv.uni-bielefeld.de/blog/uninews/entry/algae_can_draw_energy_from" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8852</link><pubDate>Tue, 20 Nov 2012 16:33:28 PDT</pubDate></item><item><title>Native plant fares well in pilot green roof research study</title><description>As the implementation of green roofs increase, a University of  Cincinnati pilot study examined which plants best thrive on the region&amp;rsquo;s  roofs during the dry, hot conditions of summer.......&amp;gt; &lt;a href="http://www.uc.edu/news/NR.aspx?id=16474" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8762</link><pubDate>Mon, 15 Oct 2012 16:25:16 PDT</pubDate></item><item><title>Scientists urge new approaches to plant research</title><description>In a paper published this week in the journal Science, a Michigan State  University professor and a colleague discuss why if humans are to  survive as a species, we must turn more to plants for any number of  valuable lessons........&amp;gt; &lt;a href="http://news.msu.edu/story/scientists-urge-new-approaches-to-plant-research/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8464</link><pubDate>Fri, 29 Jun 2012 17:02:31 PDT</pubDate></item><item><title>Indigenous peoples at forefront of climate change offer lessons on plant biodiversity</title><description>Humans are frequently blamed for deforestation and the destruction of  environments, yet there are also examples of peoples and cultures around  the world that have learned to manage and conserve the precious  resources around them. The Yanesha of the upper Peruvian Amazon and the  Tibetans of the Himalayas are two groups of indigenous peoples carrying  on traditional ways of life........&amp;gt; &lt;a href="http://www.missouribotanicalgarden.org/media/news-releases/article/264/indigenous-peoples-at-forefront-of-climate-change-offer-lessons-on-conserving-a.aspx" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8161</link><pubDate>Mon, 27 Feb 2012 16:58:53 PDT</pubDate></item><item><title>Hermetic bags save African crop, but not how experts once thought</title><description>The hermetic grain storage bags that cut off oxygen to weevils and have  saved West and Central African farmers hundreds of millions of dollars  by putting the brakes on the insects' rapid multiplication don't merely  suffocate them as once thought, a Purdue University study shows.......&amp;gt; &lt;a href="http://www.purdue.edu/newsroom/research/2012/120221MurdockPICS.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8154</link><pubDate>Wed, 22 Feb 2012 19:30:18 PDT</pubDate></item><item><title>Revealed in accurate detail, the underground world of plants</title><description>Plant and computer scientists can now study the underground world of  plants with more accuracy and clarity. The revolutionary technique will  improve our chances of breeding better crop varieties and increasing  yields.......&amp;gt; &lt;a href="http://www.nottingham.ac.uk/news/pressreleases/2012/february/the-underground-world-of-plants.aspx" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8140</link><pubDate>Fri, 17 Feb 2012 15:27:07 PDT</pubDate></item><item><title>UF research on newly formed plants could lead to improved crop fertility</title><description>A new University of Florida study shows  genomes of a recently formed plant species to be highly unstable, a  phenomenon that may have far-reaching evolutionary consequences........&amp;gt; &lt;a href="http://news.ufl.edu/2012/01/06/hybrid-chromosomes/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7995</link><pubDate>Fri, 06 Jan 2012 17:08:23 PDT</pubDate></item><item><title>Acid rain poses a previously unrecognized threat to Great Lakes sugar maples</title><description>The number of sugar maples in Upper Great Lakes forests is likely to  decline in coming decades, according to University of Michigan  ecologists and their colleagues, due to a previously unrecognized threat  from a familiar enemy: acid rain........&amp;gt; &lt;a href="http://ns.umich.edu/new/20128-acid-rain-poses-a-previously-unrecognized-threat-to-great-lakes-sugar-maples" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7928</link><pubDate>Thu, 15 Dec 2011 18:23:21 PDT</pubDate></item><item><title>Report: Herbicide atrazine spurs reproductive problems in many creatures</title><description>An international team of researchers has reviewed the evidence linking  exposure to atrazine &amp;ndash; an herbicide widely used in the U.S. and more  than 60 other nations &amp;ndash; to reproductive problems in animals. The team  found consistent patterns of reproductive dysfunction in amphibians,  fish, reptiles and mammals exposed to the chemical.......&amp;gt; &lt;a href="http://news.illinois.edu/news/11/1128atrazine_ValBeasley.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7872</link><pubDate>Mon, 28 Nov 2011 17:19:33 PDT</pubDate></item><item><title>Bat plant could give some cancers a devil of a time</title><description>In a new study published this month in the Journal of the American  Chemical Society, researchers with The University of Texas Health  Science Center at San Antonio have pinpointed the cancer-fighting  potential in the bat plant, or Tacca chantrieri........&amp;gt; &lt;a href="http://www.uthscsa.edu/hscnews/singleformat2.asp?newID=3991" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7861</link><pubDate>Tue, 22 Nov 2011 17:07:03 PDT</pubDate></item><item><title>Plant with 'eggbeater' testure inspires waterproof coating</title><description>A floating weed that clogs waterways around  the world has at least one  redeeming feature: It&amp;rsquo;s inspired a high-tech  waterproof coating  intended for boats and submarines.......&amp;gt; &lt;a href="http://researchnews.osu.edu/archive/eggbeater.htm" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7819</link><pubDate>Thu, 10 Nov 2011 17:17:06 PDT</pubDate></item><item><title>Genome-scale network of rice genes to speed the development of biofuel crops</title><description>The first genome-scale model for predicting the functions of genes and  gene networks in a grass species has been developed by an international  team of researches that includes scientists with the U.S. Department of  Energy (DOE)&amp;rsquo;s Joint BioEnergy Institute (JBEI), a multi-institutional  partnership led by Lawrence Berkeley National Laboratory (Berkeley  Lab).&amp;nbsp; Called RiceNet, this systems-level model of rice gene  interactions should help speed the development of new crops for the  production of advanced biofuels, as well as help boost the production  and improve the quality of one of the world&amp;rsquo;s most important food  staples........&amp;gt;&lt;a href="http://newscenter.lbl.gov/news-releases/2011/11/02/ricenet/" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7788</link><pubDate>Wed, 02 Nov 2011 16:40:17 PDT</pubDate></item><item><title>Protein plays role in helping plants see light</title><description>Plants do not have eyes or legs, yet they are able to "see" and move  toward and away from light. This ability, called phototropism, is  controlled by a series of molecular-level signals between proteins  inside and between plant cells. In a paper published in &lt;em&gt;The Plant Cell,&lt;/em&gt; University of Missouri scientists report for the first time the elusive  role a critical protein plays in this molecular signaling pathway that  regulates phototropism in plants.
Directional light that induces phototropism is sensed by a plant  through the action of two light-sensing proteins, phototropin 1 and  phototropin 2. These proteins act as photoreceptors and initiate the  phototropic signaling response in conjunction with a third protein,  called NPH3.
"If the phototropic signaling pathway were like a baseball game, the  phototropins would be the pitcher and NPH3 the catcher who work  together to coordinate the signal, or pitch," says Mannie Liscum, a  professor of biological sciences in the College of Arts and Science and  in the Christopher S. Bond Life Sciences Center. "Prior to this study,  no one knew how NPH3 and the phototropins cooperated to facilitate the  signal."
Using a combination of genetic and biochemical methods, Liscum and  colleagues found that NPH3 functions as part of a protein complex that  modifies phototropin 1 by the addition of a small protein "tag" called  ubiquitin. Either a single ubiquitin or a chain of ubiquitin proteins is  added, depending on the amount of light the plant "sees."
If we continue the baseball analogy, ubiquitin is the hand signals NPH3  uses to coordinate with phototropin 1 the type and sequence of signals  depending on the particular lighting situation.
"In low-light conditions, phototropin 1 is modified with single  ubiquitin proteins and then apparently moves to a different part of the  cell. In high-light conditions, phototropin 1 is modified with multiple  ubiquitin proteins and is degraded by the cell to shut down further  signaling," says Liscum.
The finding may have applicability to research beyond phototropism in plants.
"The tagging of proteins with ubiquitin represents a common  biochemical event throughout the biological world.  In fact, many human  disease pathologies are associated with alterations in  ubiquitin-tagging," says Liscum. "Our studies identifying a single  enzyme complex that is capable of modifying a substrate in different  ways simply based on the environmental conditions may therefore have  implications on fields far askew from agriculture."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7713</link><pubDate>Wed, 12 Oct 2011 17:51:20 PDT</pubDate></item><item><title>New study shows how trees clean the air in London</title><description>New research by scientists at the University of Southampton has shown  how London's trees can improve air quality by filtering out pollution  particulates, which are damaging to human health.
A paper published this month in the journal &lt;em&gt;Landscape and Urban Planning&lt;/em&gt; indicates that the urban trees of the Greater London Authority (GLA)  area remove somewhere between 850 and 2000 tonnes of particulate  pollution (PM10) from the air every year.
An important development in this research, carried out by Dr Matthew  Tallis, is that the methodology allows the prediction of how much  pollution will be removed in the future as the climate and pollution  emissions change. This shows the real benefits of the planned increase  in the number of street trees in London and throughout England,  including the GLA's plan to increase the area of urban trees by 2050   and the current government's 'Big tree plant' initiative.
The research found that the targeting of tree planting in the most  polluted areas of the GLA area and particularly the use of a mixture of  trees, including evergreens such as pines and evergreen oak, would have  the greatest benefit to future air quality in terms of PM10 removal.
One of the paper's authors Professor Gail Taylor explains: "Trees have evolved to remove CO&lt;sub&gt;2&lt;/sub&gt; from the atmosphere, so it's not surprising that they are also good at  removing pollutants. Trees which have leaves the whole year are exposed  to more pollution and so they take up more. Using a number of different  tree species and modelling approaches, the effectiveness of the tree  canopy for clean air can be optimised."
This study presents predictions of particulate (PM10) uptake in  future climate and for five tree planting scenarios in London. Using  seasonal rather than hourly data was shown to have little impact on  modelled annual deposition of pollution (PM10) to urban canopies,  suggesting that pollution uptake can be estimated in other cities and  for the future where hourly data are not available.
Co-author Peter Freer-Smith, Chief Scientist for Forest Research  (Forestry Commission) and visiting professor at the University of  Southampton, says: "We know that particulates can damage human health,  for example exacerbating asthma and this reduction in exposure could  have real benefits in some places, such as around the edge of school  playgrounds.  Urban greenspace and trees give a wide range of benefits  and this study confirms that improving air quality is one of them and  will also help us to get the most out of this benefit in future."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7688</link><pubDate>Wed, 05 Oct 2011 17:22:03 PDT</pubDate></item><item><title>St. Michael's studies Toronto community services</title><description>Torontonians want non-profit organizations to provide programs and  services in their neighbourhoods that are relevant to their needs,  held  at convenient times and locations and have stable funding, a research  study has found.
People under 25 and without post-secondary education also want these organizations to help them find jobs and become financially stable, the study found.
The study was conducted between December and July by St. Michael's  Hospital's Centre for Research on Inner City Health (CRICH). Researchers  asked Torontonians what they thought the city should pay attention to  when it comes to community services in their neighbourhoods, ranging  from boys and girls clubs to community gardens, drop in programs for  seniors, or mentorship and job skills programs for newcomers and youths.
Patricia O'Campo, one of the authors of the study and the director  of CRICH, said the results were particularly significant because the  people surveyed were asked open-ended questions about what was important  to them and what the city should pay attention to.  Respondents  provided their own answers rather than choosing from a list of options  selected by the surveyors.
O'Campo, an epidemiologist, said the results were also important  because they were consistent across all neighbourhoods of the city and  ethnic and demographic groups.
"Torontonians don't want to have to leave their neighbourhoods to  get the programs they need," O'Campo said. "They want programs to be  available and accessible. They also want community organizations to have  stable funding, so services aren't interrupted because they run out of  money."
The results come as Toronto City Council debates possibly  wide-ranging service and program cuts in an effort to eliminate a budget  deficit.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7651</link><pubDate>Fri, 23 Sep 2011 17:02:58 PDT</pubDate></item><item><title>Firewood movement leading cause of oak infestation in San Diego County</title><description>A catastrophic infestation of the goldspotted oak borer, which has  killed more than 80,000 oak trees in San Diego County in the last  decade, might be contained by controlling the movement of oak firewood  from that region, according to researchers at the University of  California, Riverside........&amp;gt; &lt;a href="http://newsroom.ucr.edu/2715" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7576</link><pubDate>Fri, 02 Sep 2011 18:49:38 PDT</pubDate></item><item><title>New component of a plant steroid-activated pathway discovered</title><description>Plant biologists have been working for years to nail down the series  of chemical signals that one class of plant hormones, called  brassinosteroids, send from a protein on the surface of a plant cell to  the cell's nucleus. New research from Carnegie scientists Tae-Wuk Kim  and Zhiyong Wang, with contributions from the University of California  San Francisco, isolated another link in this chain. Fully understanding  the brassinosteroid pathway could help scientists better understand  plant growth and help improve food and energy crop production.
Brassinosteroids are found throughout the plant kingdom and regulate  many aspects of growth and development, as well as resistance to  external stresses. Mutant plants that are deficient in brassinosteroids  show defects at many phases of the plant life cycle including reduced  seed germination, irregular growth in the absence of light, dwarfism,  and sterility.
The series of proteins involved in a plant cell detecting the  presence of brassinosteroids and using this information to respond to  the plant's environment is one of the best-studied aspects of plant  cellular physiology and biochemistry. Previous research had identified a  pathway of chemical signals that starts when a brassinosteroid binds to  a receptor on the surface of a plant cell and activates a cascade of  activity that consists of adding and removing phosphates from a series  of proteins.
The research team was able to identify a new aspect of this pathway,  a protein called Constitutive Differential Growth1, or CDG1. Their work  will be published in &lt;em&gt;Molecular Cell&lt;/em&gt; on August 19.
Using an extensive array of research techniques, they determined  that when activated by the brassinosteroid receptor, CDG1 adds a  phosphate to another protein called BSU1. It was already known that the  BSU1 protein in turns deactivates a third protein called BIN2. When BIN2  is active it inhibits two other proteins called BZR1 and BZR2, which  are part of a special class called transcription factors. When they are  inactive, they are unable to enter the plant cell's nucleus. But once  BIN2 is deactivated by BSU1, they are able to bind directly to DNA  molecules inside the nucleus and promote a wide variety of gene  activity.
"Together with our previous work, these results provide the detailed  mechanisms of brassinosteroid signaling," Wang said. "Because this  system of brassinosteroid-activated proteins is one of the  best-understood chemical pathways in plant physiology, these results  could help scientists understand many other plant cell systems."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7519</link><pubDate>Thu, 18 Aug 2011 16:28:40 PDT</pubDate></item><item><title>Biologists discover an 'evening' protein complex that regulates plant growth</title><description>Farmers and other astute observers of nature have long known that  crops like corn and sorghum grow taller at night. But the biochemical  mechanisms that control this nightly stem elongation, common to most  plants, have been something of a mystery to biologists&amp;mdash;until now.
In this week's early online publication of the journal &lt;em&gt;Nature,&lt;/em&gt; biologists at the University of California, San Diego report their  discovery of a protein complex they call the "evening complex" that  regulates the rhythmic growth of plants during the night. More  importantly, the biologists show how this protein complex is intricately  coordinated through the biological clock with the genes that promote  stem elongation in a way that could enable plant breeders to engineer  new varieties of crops that grow faster, produce greater yields of food  or generate more biomass per acre of land for conversion into biofuels.
"This discovery gives us a molecular understanding of how the  biological clock is regulating cyclic growth in plants," said Steve Kay,  dean of UC San Diego's Division of Biological Sciences, who headed the  research effort. "And it instantly gives us a handle on how we might  manipulate and control plant yield or biomass deposition."
While most people assume that plants grow at a slow and steady rate  throughout the day and night, Charles Darwin and others more than a  century ago observed that they actually grow in spurts late at night,  with plant stems elongating fastest in the hours just before dawn.
"Plants actually grow rhythmically," said Kay. "Some plants, like  sorghum, have the ability to elongate a centimeter or more each night."
The UCSD biologists initially focused their attention on three genes  from a tiny mustard plant called Arabidopsis, which is used by  geneticists as a laboratory model for plants. When they are disabled by  mutations, these three genes disrupt the plant's biological clock and  promote both stem elongation and early flowering.
"These three genes have been of intense interest because the loss of  function in each one of them kills the biological clock, causes a long  hypocotyl, or juvenile stem, and tends to cause early flowering," said  Kay. "We thought that maybe their function was related. So this  investigation was basically started to figure out what these three genes  do."
The answer to that seemingly simple question took the biologists  more than six years to disentangle. Their efforts were led by three  postdoctoral fellows in Kay's lab: Dmitri Nusinow, Anne Helfer and  Elizabeth Hamilton.
"Circadian clocks control the timing of an extraordinary variety of  developmental and physiological processes in humans and other species,  but figuring out how they do this is tough," said Laurie Tompkins, who  oversees biological clock grants at the National Institutes of Health's  National Institute of General Medical Sciences, which funded the  research. "Arabidopsis is ideal for this sort of analysis, since  researchers can use a variety of sophisticated genetic and biochemical  tools to study molecular interactions at different times of day and then  easily observe the tiny plant's development."
Because the three genes&amp;mdash;Early Flowering3 (or ELF3), ELF4 and  LUX&amp;mdash;have biological activities that peak in the early evening, the UCSD  biologists wondered if the three genes acted together in a protein  complex. Through a series of experiments in yeast cells, they determined  the three genes produced proteins that did interact with one another,  but in a specific way. ELF3 served as a docking protein that brought  together ELF4 and LUX, but the latter two did not interact with each  other without ELF3's help.
This protein complex was dubbed the "evening complex" by the UCSD  scientists, who verified in Arabidopsis that not only did the biological  activities of the three components of this protein complex peak in the  evening, but so did the formation of the evening complex itself.
The researchers then sought to answer the question of what the  physiological role of this protein complex could be in plants. One main  clue pointed them in the right direction: When any one of the three  genes controlling this protein complex is disabled, plants end up with  grossly elongated stems.
"This protein complex is clearly acting like the brakes on growth,"  said Kay. "So when we mutate any one of these genes the plants elongate  much more."
In another set of experiments, the researchers demonstrated that the  evening complex puts the brakes on the activity of two genes in  plants&amp;mdash;PIF4 and PIF5&amp;mdash;that are important in promoting plant growth.
"What we show in our paper is that the evening complex binds to the  promoters of PIF4 and PIF5 and, at the end of the day and through the  early part of the night, prevents the plants from growing," said Kay.  "And when the levels of the evening complex begin to drop, PIF4 and PIF5  are expressed and drive plant expression programs that support stem  elongation, and the brakes on plant growth are taken off."
In this new model of plant growth developed by the scientists, PIF4  and PIF5 control the gas pedal that activates plants to grow, while the  three genes that produce the evening complex act as the brakes and work  with the plant's biological clock to permit the most rapid growth in the  late evening and early morning hours.
"Nobody knew how this cyclic regulation of plant growth worked on a  molecular level, but this must be one of the major mechanisms," said  Kay. "This really gives us a molecular understanding of how the  biological clock is regulating cyclic growth in plants."
Why plants time their diurnal cycle to grow most rapidly late at  night and in the wee hours of the morning is still a mystery, but Kay  suspects it could be when resources are most available since plants  store what they produce from photosynthesis during the day as starch,  then break that starch and protein down at night to make them available  for growth.
"Plants have to coordinate their growth with the availability of  resources," he said. "There's really no advantage for these plants just  to get bigger and bigger if they're not coordinating their metabolic  resources, which come cyclically with photosynthesis each day. So plants  grow rhythmically presumably to coordinate growth with available  metabolic resources."
As scientists gain a better understanding of these plant growth  control mechanisms, the potential commercial applications to agriculture  could be as broad as they are significant. The discovery of the  mechanisms of the evening complex should eventually provide plant  geneticists with a new way to optimize the growth of crops so they can  produce more food or more biomass per acre for biofuel production.
"What this discovery tells us is that the circadian clock is  controlling tens of millions of tons of biomass deposition every night  in the United States that could be used for bioenergy," said Kay. "Now  that we understand what the gas and the brakes are in controlling plant  growth, we can manipulate those to maximize biomass deposition. We could  do it by putting the gas on more or putting the brakes on less or  probably in a more sophisticated way by combining the gas and brakes so  that we allow the plant to maximize available nutrients, which will  allow it to maximize biomass deposition. This could be a way to optimize  plant growth for a particular environment where we don't want to add  additional nutrients to the soil."
Kay said another totally unrelated application for the evening  complex could be in making plants, particularly food crops, more  tolerant to cold temperatures or freezing.
"When you make mutations to these genes, the plants are less  tolerant to freezing and low temperatures," he said. "So we think the  evening complex is likely to have a role in cold tolerance and that's  something else we're going to be investigating."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7387</link><pubDate>Wed, 13 Jul 2011 17:34:39 PDT</pubDate></item><item><title>Simple little spud helps scientists crack potato's mighty genome</title><description>The Potato Genome Sequencing Consortium (PGSC), a team of scientists  from institutions worldwide, including Virginia Tech, has published its  findings in the Sunday July 10 online issue of the journal &lt;a href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature10158.html"&gt;&lt;em&gt;Nature&lt;/em&gt;&lt;/a&gt;.
The successful sequencing of the genome of the world's third most  important crop began when Richard Veilleux, who is the Julian and  Margaret Gary Professor of Horticulture in the College of Agriculture  and Life Sciences at Virginia Tech, wondered if the then new  applications of plant tissue culture could be used to develop parent  lines for hybrid potatoes. The concept was developed from his doctoral  research, completed in 1981 at the University of Minnesota.
Most modern crop varieties are hybrids because hybrids are usually  more vigorous than either parent. For example, with corn, a variety with  desirable characteristics is self-pollinated for many generations, and  the resulting seed is grown and crossbred with another similarly  developed line with a different genetic background.
Since potatoes do not self-pollinate, Veilleux engineered inbred  lines from immature pollen extracted from flower buds by using plant  tissue culture. The result, potato plants with half the chromosomes of  the parent, was completely sterile. "Their chromosomes have to be  doubled, up to 24, which results in plants with completely identical  pairs of chromosomes &amp;ndash; a homozygous inbred line," said Veilleux. "In one  cycle, you have accomplished what it takes five generations to do to  create a maize inbred line the old-fashioned way."
Since that initial success, he has conducted years of basic research  to improve these lines as building blocks for hybrid potato seed,  supported by the U.S. Department of Agriculture through Hatch grants,  among other funding. Over the years, he reported at international  meetings on his progress toward developing a vigorous homozygous inbred  line with desirable traits for hybrid parenthood.
By 2006, when an international team formed the Potato Genome  Sequencing Consortium to attempt to sequence the genome of the potato,  Veilleux's simple little spuds were poised for fame as the first potato  to have its genome sequenced.
But first, the consortium, made up of groups at institutions from 14  countries, wanted to sequence a more popular and productive tuber, more  resembling what is found on dinner tables worldwide. The consortium was  working with a diploid variety that, like Veilleux's potato, has only  24 chromosomes. However, the pairs of chromosomes of the selected line  are not identical; they carry variations of similar genes, resulting in  thousands of differences in the base pairs &amp;ndash; or rungs on the DNA  ladder-- between chromosome pairs.
Modern sequencing technology is a time saver, spitting out 50-base  pair sequences millions at a time. But the well-regarded modern potato  has 840 million base pairs. The variation between pairs of chromosomes  essentially doubled that. Assembling the puzzle was becoming  overwhelming.
Then scientists within the consortium remembered Veilleux's  presentations at international meetings about a simple little potato he  was developing with hopes of it someday parenting a new hybrid.
Sanwen Huang with the Chinese Academy of Agricultural Science, and  Robin Buell of Michigan State University, both members of the consortium  steering committee, each approached Veilleux for permission to use his  simpler homozygous diploid potatoes for sequencing.
"I said, 'sure', and was invited to become a member of the consortium," said Veilleux.
Veilleux sent his plant material directly to Buell, whereas Huang  obtained DNA of the same potato from Peru, where Veilleux had sent  cultures years before for breeding studies by Meredith Bonierbale of the  International Potato Center (CIP). DNA tests were done to make sure  that the potatoes Buell and Huang obtained were the same &amp;ndash; which they  were.
According to the consortium news release, "Analysis of the genome  sequence data has revealed that the potato genome contains approximately  39,000 protein coding genes. For over 90 percent of the genes the  location on one of the 12 chromosomes is now known. The analysis also  reveals that the potato genome has undergone extensive genome  duplication through evolution&amp;hellip; The data also show clear evidence for how  expansion of particular gene families has contributed to the evolution  of the potato tuber &amp;ndash; the edible storage organ that is the most striking  feature of this important and fascinating plant. "
"We can thank many Hokies, who have been paid as undergraduate hourly  employees for decades on the project to maintain the potato collection  in tissue culture," said Veilleux. "Research specialist Suzanne Piovano  trained them to conduct routine subcultures to fresh medium every few  weeks and to keep the confusing potato identities straight. The many  potato crops required for the project have been grown under the  vigilance of the horticulture department's capable greenhouse manager,  Jeff Burr."
Veilleux's original potatoes actually came from South America &amp;ndash; a  diploid species called phureja that produces potatoes of many colors,  textures, and tastes.
Now, the sequence of Veilleux's little potato will be used as a  draft against which the genome sequences of more complicated tubers will  be compared. "Sequencing technology is getting better, and now that we  have sequenced this one potato, it is kind of easy," he said. "There are  all kinds of spinoff studies that can be done, such as looking at the  DNA sequence variation in the genomes of different kinds of potatoes.
"These sequences will allow scientists to locate genes for desired  traits and develop new varieties. All potatoes have essentially the same  genes but the forms of the genes vary so that similar genes found in  Idaho Russets or Red Norlands on the supermarket shelves can be compared  to those in the sequenced line to determine how differences in the  genetic code affect traits that make up the quality of commercial  potatoes," Velleux said.
What about using inbred lines to produce hybrid varieties? That may  never happen, but Veilleux said he will keep trying. Just this spring,  students in his graduate class in advanced plant genetics were working  in Virginia Tech's greenhouses, crossing commercial varieties and  hybrids from his inbred lines. Maybe the next crop of hybrids will find  their way onto tables eventually.
The project is also resulting in new collaborations. "Dr. Huang  wants to work with me to find out what genetic material was left behind  in the process of creating the inbred lines," said Veilleux.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7377</link><pubDate>Mon, 11 Jul 2011 17:44:38 PDT</pubDate></item><item><title>What is good for you is bad for infectious bacteria</title><description>Plants are able to protect themselves from most bacteria, but some  bacteria are able to breach their defences. In research to be published  in &lt;em&gt;Science&lt;/em&gt; on Friday, scientists have identified the genes used by some strains of the bacterium &lt;em&gt;Pseudomonas&lt;/em&gt; to overwhelm defensive natural products produced by plants of the mustard family, or crucifers.
"Microbes only become pathogens when they find a way to infect a  host and overwhelm the host defences," said lead author Dr Jun Fan from  the John Innes Centre on the Norwich Research Park.
"Our findings answer some important questions about host-pathogen biology."
The scientists have confirmed that the chemicals used by cruciferous  plants to defend against bacteria are isothiocyanates, nitrogen and  sulphur-containing organic compounds produced by plants of the mustard  family, such as cabbage, broccoli and Brussels sprouts. These potent  molecules have antioxidant, anticancer and anti-inflammatory properties  in humans.
Isothiocyanates are released by the plant when it is challenged or  eaten. They had previously been shown to be active against bacteria but  this is the first time their essential role has been successfully tested  using real plants. Without this class of compounds, crucifers would be  more vulnerable to disease from a much wider variety of bacteria.
Isothiocyanates also provide a chemical barrier to harmful fungi and a toxic defence warning to insects and other herbivores.
The team of scientists from JIC and the University of Edinburgh  found that bacterial pathogens carrying the sax genes, thought to be  involved in detoxification and removal of isothiocyanates, were able to  overcome these defences.
Understanding how some bacterial strains become specialised to  overcome plant resistance will help scientists identify new ways to  improve crop plants.
"These discoveries have a broader significance for current efforts  to increase food security," said co-author Dr Peter Doerner from  Edinburgh University.
"They define a strategy for sustainable disease control in  agriculture by stimulating the production and variety of natural  products in various crop plants."
The research was initiated by former JIC director Professor Chris Lamb and he is an author on the paper.
"Chris supported the research for over a decade up until his death in 2009," said Dr Fan.
"This is a good example of his pursuit of excellence and relevance in scientific research."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6839</link><pubDate>Fri, 04 Mar 2011 03:21:05 PDT</pubDate></item><item><title>Texas leafcutter ants aided, but also limited, by cold-tolerant fungus crops, research shows</title><description>Texas leafcutter ants farm crops of fungus that evolved cold  tolerance to Texas winters, just as northern farmers cultivate cold  weather crops, researchers from The University of Texas at Austin show  in a new paper published in the journal PNAS Early Edition.
Though the cold tolerant fungus gives the ants the ability to  maintain winter gardens, the fungus is still sensitive enough to cold it  limits the ant's ability to spread farther northward.
"The same is true for human farmers," says Ulrich Mueller, professor  of biology. "Some of our crops come originally from the tropics, and  humans have had to select them over time to grow in colder climates. But  we are still limited by our abilities to select and adapt crops to  local conditions."
Mueller and his colleagues found that even within Texas the fungus  is more tolerant of cold at its northern edge near Dallas, and less  tolerant of cold at its southern edge near Brownsville.
At Fort Belknap, just northwest of Dallas, Mueller says the ants "are just hanging on."
Leafcutter ants are largely tropical, and the Texas leafcutter ant,  Atta texana, is one of only three leafcutter ant species found in the  United States. The species arrived in the region about 10,000 years ago  after the retreat of the glaciers and the end of the last Ice Age.
"The ants may have only been in Fort Belknap for a few hundreds or thousands of years," Mueller says.
The ant's symbiotic relationship with the cold tolerant fungus  clearly permits it to survive in the more temperate environments of  Texas.
The finding provides a perspective on symbiotic relationships, which  are normally thought of as being beneficial to both organisms.
"We normally think that forging a symbiotic relationship enriches  lives&amp;mdash;that each organism is helping the other," says Mueller. "But we  have found that this can be the opposite. In the tropics, the symbiosis  between the leafcutter ants and their fungal crops helped to broaden the  ants' ecological niches. In the Texas leafcutter, the symbiotic  relationship also constrains them."
Texas is a particularly interesting laboratory for studies of local  species adaptations because of its unique ecological conditions. It is  the only state in the U.S. where an unusually steep precipitation  gradient from east to west crosses a steep temperature gradient from  north to south, ranging from temperate to subtropical.
"Texans are uniquely positioned to monitor the effect of  environmental change on U.S. biodiversity," says Mueller. "It will be  interesting to see what happens with these ants over the next 10 to 20  years with global warming. Will they expand to Oklahoma and across the  Mississippi River, or will cold snaps like those we just experienced  knock them back?"</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6763</link><pubDate>Wed, 23 Feb 2011 03:17:38 PDT</pubDate></item><item><title>Plant breeding is being transformed by advances in genomics and computing</title><description>The arrival of affordable, high throughput DNA sequencing, coupled  with improved bioinformatics and statistical analyses is bringing about  major advances in the field of molecular plant breeding.  Multidisciplinary breeding programs on the world's major crop plants are  able to investigate genome-wide variations in DNA sequences and link  them to the inheritance of highly complex traits controlled by many  genes, such as hybrid vigor. Furthermore, there has been a step-change  in speed and cost-effectiveness.  What previously took six generations  to achieve can now be done in two, delivering massive time and resource  savings. This has made molecular plant breeding feasible on marginal  crops including medicinal plants and crops of the developing world.
Agriculture faces demands to sustainably produce enough food for an  expanding world population and to improve the nutritional quality of  food crops, as well as to provide non-food crops, e.g. for the biofuels  industry. The progress in molecular plant breeding can help meet these  demands by;
&lt;ul&gt;
&lt;li&gt;shortening the time it takes to domesticate new crops from semi-wild plants, &lt;/li&gt;
&lt;li&gt;tailoring existing crops to meet new requirements, such as nutritional enhancement or climate change, &lt;/li&gt;
&lt;li&gt;rapidly incorporating valuable traits from wild relatives into established crops, &lt;/li&gt;
&lt;li&gt;allowing plant breeders to work with highly complex traits, such as hybrid vigour and flowering, &lt;/li&gt;
&lt;li&gt;making it feasible to work on research-neglected  "orphan" crops. &lt;/li&gt;
&lt;/ul&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6751</link><pubDate>Mon, 21 Feb 2011 03:30:14 PDT</pubDate></item><item><title>Plants that can move inspire new adaptive structures</title><description>The Mimosa plant, which folds its leaves when they're touched, is  inspiring a new class of adaptive structures designed to twist, bend,  stiffen and even heal themselves. University of Michigan researchers are  leading their development.
Mechanical engineering professor Kon-Well Wang will present the  team's latest work Feb. 19 at the American Association for the  Advancement of Science's 2011 Annual Meeting in Washington D.C. He will  also speak at a news briefing earlier that day. Wang is the Stephan P.  Timoshenko Collegiate Professor of Mechanical Engineering and chair of  the Department of Mechanical Engineering.
"This is quite different from other traditional adaptive materials  approaches," Wang said. "In general, people use solid-state materials to  make adaptive structures. This is really a unique concept inspired by  biology."
Researchers at U-M and Penn State University are studying how plants  like the Mimosa can change shape, and they're working to replicate the  mechanisms in artificial cells. Today, their artificial cells are  palm-size and larger. But they're trying to shrink them by building them  with microstructures and nanofibers. They're also exploring how to  replicate the mechanisms by which plants heal themselves.
"We want to put it all together to create hyper-cellular structures with circulatory networks," Wang said.
The Mimosa is among the plant varieties that exhibit specialized  "nastic motions," large movements you can see in real time with the  naked eye, said Erik Nielsen, assistant professor in the U-M Department  of Molecular, Cellular and Developmental Biology.
The phenomenon is made possible by osmosis, the flow of water in and  out of plants' cells. Triggers such as touch cause water to leave  certain plant cells, collapsing them. Water enters other cells,  expanding them. These microscopic shifts allow the plants to move and  change shape on a larger scale.
It's hydraulics, the researchers say.
"We know that plants can deform with large actuation through this  pumping action," Wang said. "This and several other characteristics of  plant cells and cell walls have inspired us to initiate ideas that could  concurrently realize many of the features that we want to achieve for  adaptive structures."
Nielsen believes nastic movements might be a good place to start  trying to replicate plant motions because they don't require new growth  or a reorganization of cells.
"These rapid, nastic motions are based on cells and tissues that are  already there," Nielsen said. "It's easy for a plant to build new cells  and tissues during growth, but it's not as easy to engineer an object  or machine to completely change the way it's organized. We hope studying  these motions can inform us about how to make efficient adaptive  materials that display some of the same types of flexibility that we see  in biological systems."
When this technology matures, Wang said it could enable robots that  change shape like elephant trunks or snakes to maneuver under a bridge  or through a tunnel, but then turn rigid to grab a hold of something. It  also could lead to morphing wings that would allow airplanes to behave  more like birds, changing their wing shape and stiffness in response to  their environment or the task at hand.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6750</link><pubDate>Mon, 21 Feb 2011 03:28:53 PDT</pubDate></item><item><title>Plants cloned as seeds</title><description>Plants have for the first time been cloned as seeds. The research by  aUC Davis plant scientists and their international collaborators,  published Feb. 18 in the journal &lt;em&gt;Science&lt;/em&gt;, is a major step towards making hybrid crop plants that can retain favorable traits from generation to generation.
Most successful crop varieties are hybrids, said Simon Chan,  assistant professor of plant biology at UC Davis and an author of the  paper. But when hybrids go through sexual reproduction, their traits,  such as fruit size or frost resistance, get scrambled and may be lost.
"We're trying to make a hybrid that breeds true," Chan said, so that   plants grown from the seed would be genetically identical to one  parent.
Some plants, especially fruit trees, can be cloned from cuttings,  but this approach is impractical for most crops.  Other plants,  especially weeds such as hawkweed and dandelions, can produce true seeds  that are clones of themselves without sexual reproduction -- a still  poorly understood process called apomixis.
The new discovery gets to the same result as apomixis, although by a different route, Chan said.
Normally, eggs and sperm are haploid -- they have half the number of  chromosomes of the parent. The fertilized egg and the adult plant it  grows into are diploid -- containing a full complement of chromosomes,  half contributed by each parent.
Chan and his colleagues focused their work on the laboratory plant &lt;em&gt;Arabidopsis&lt;/em&gt;,  which has certain genetic mutations that allow it to produce diploid  eggs without sexual recombination. These eggs have the same genes and  number of chromosomes as their parents. But those eggs cannot be grown  into adult plants without fertilization by sperm, which adds another  parent's set of chromosomes.
Last year, Chan and UC Davis postdoctoral researcher Maruthachalam Ravi showed that they could breed haploid &lt;em&gt;Arabidopsis&lt;/em&gt; plants that carried chromosomes from only one parent. They introduced a  genetic change so that after the eggs were fertilized, the chromosomes  from one of the parents were eliminated. Such haploid plants would  reduce the time needed to breed new varieties.
In the new study, Chan's lab, with colleagues from India and France, crossed these &lt;em&gt;Arabidopsis&lt;/em&gt; plants programmed to eliminate a parent's genes with either of two mutants that can produce diploid eggs.
The result? In about one-third of the seeds produced, the diploid  eggs were successfully fertilized, then the chromosomes from one parent  were eliminated, leaving a diploid seed that was a clone of one of its  parents.
Ravi described the result as a step on the way towards artificial  apomixis. The team hopes to produce crop plants, such as lettuce and  tomato, that can fertilize themselves and produce clonal seeds.  Applications for provisional patents on the work have been filed.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6736</link><pubDate>Fri, 18 Feb 2011 03:21:11 PDT</pubDate></item><item><title>The production of plant pollen is regulated by several signaling pathways</title><description>Flowers are no ornamental luxury to plants; after all, they hold the  male and female reproductive organs. The male pollen is produced in the  stamens and the carpel bears the female ovule. The fusion of the two  produces a germinable embryo that ensures the reproduction of the plant.  Plants can only bloom if a radical transition occurs during their  development. This stops the production of leaves and instead causes the  reproductive cells that are equipped with a single set of chromosomes to  form sexually distinctive reproductive organs. For optimal  reproduction, this must coincide with certain external conditions, such  as light and temperature. However, sensitivity to the external  conditions must not be so great that it prevents blooming if the  environmental conditions are not optimal.......&amp;gt; &lt;a href="http://www.mpg.de/1053638/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6572</link><pubDate>Thu, 27 Jan 2011 03:21:40 PDT</pubDate></item><item><title>Nailing down a crucial plant signaling system</title><description>Plant biologists have discovered the last major element of the series  of chemical signals that one class of plant hormones, called  brassinosteroids, send from a protein on the surface of a plant cell to  the cell's nucleus. Although many steps of the pathway were already  known, new research from a team including Carnegie's Ying Sun and  Zhiyong Wang fills in a missing gap about the mechanism through which  brassinosteroids cause plant genes to be expressed. Their research,  which will be published online by &lt;em&gt;Nature Cell Biology&lt;/em&gt; on January 23, has implications for agricultural science and, potentially, evolutionary research.
"Brassinosteroids are found throughout the plant kingdom and  regulate many aspects of growth and development, as well as resistance  from external stresses," said Wang. "Mutant plants that are deficient in  brassinosteroids show defects at many phases of the plant life cycle,  including reduced seed germination, irregular growth in the absence of  light, dwarfism, and sterility."
Previous research had identified a pathway of chemical signals that  starts when a brassinosteroid binds to a receptor on the surface of a  plant cell and activates a cascade of activity that consists of adding  and removing phosphates from a series of proteins.
When brassinosteroids are not present, a protein in this pathway  called BIN2 acts to add phosphates to two other proteins called BZR1 and  BZR2, which are part of a special class of proteins called  transcription factors. The phosphates inhibit the transcription factors.  But when a brassinosteroid binds to the cell-surface receptor, BIN2 is  deactivated, and as a result phosphates are removed from the two  transcription factors. As a result, BZR1 and BZR2 can enter the cell's  nucleus, where they bind directly to DNA molecules and promote a wide  variety of gene activity.
Before this new research, the protein that detaches the phosphates  and allows BZR1 and BZR2 to work was unknown. Using an extensive array  of research techniques, the team was able to prove that a protein called  protein phosphatase 2A (PP2A) is responsible.
"We discovered that PP2A is a key component of the brassinosteroid  signaling pathway," Wang said. "This discovery completes the core  signaling module that relays extracellular brassinosteroids to cue  activity in the nucleus."
Further research is needed to determine whether brassinosteroid  binding activates PP2A, or just deactivates BIN2, thus allowing PP2A to  do this job. Additionally, PP2A is involved in a plant's response to  gravity and light, among other things.
This aspect of the brassinosteroid signaling pathway bears some  surprising resemblances to signaling pathways found in many members of  the animal kingdom. More research could demonstrate details of the  evolutionary split between non-protozoan animals and plants.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6548</link><pubDate>Mon, 24 Jan 2011 03:23:51 PDT</pubDate></item><item><title>Grape ingredient resveratrol increases beneficial fat hormone</title><description>Resveratrol, a compound in grapes, displays antioxidant and other  positive properties. In a study published this week, researchers at the  UT Health Science Center San Antonio describe a novel way in which  resveratrol exerts these beneficial health effects.&lt;br /&gt;&lt;br /&gt;Resveratrol  stimulates the expression of adiponectin, a hormone derived from cells  that manufacture and store fat, the team found. Adiponectin has a wide  range of beneficial effects on obesity-related medical complications,  said senior author Feng Liu, Ph.D., professor of pharmacology and member  of the Barshop Institute of Longevity and Aging Studies at the Health  Science Center. &lt;br /&gt;&lt;br /&gt;Both adiponectin and resveratrol display anti-obesity, anti-insulin resistance and anti-aging properties.......&amp;gt; &lt;a href="http://www.uthscsa.edu/hscnews/singleformat2.asp?newID=3666" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6443</link><pubDate>Sat, 08 Jan 2011 17:34:56 PDT</pubDate></item><item><title>University of Illinois research makes plant breeding easier</title><description>University of Illinois research has resulted in the development of a  novel and widely applicable molecular tool that can serve as a road map  for making plant breeding easier to understand. Researchers developed a  unified nomenclature for male fertility restorer (RF) proteins in higher  plants that can make rapid advancements in plant breeding.
"Understanding the mechanism by which RF genes suppress the male  sterile phenotype and restore fertility to plants is critical for  continued improvements in hybrid technology," said Manfredo J.  Seufferheld, U of I assistant professor of crop sciences.
To reach this goal, Seufferheld teamed up with post-doctoral  researchers Simeon O. Kotchoni and Emma W. Gachomo of Purdue University,  and Jose C. Jimenez-Lopez of the Estacion Experimental del Zaidin,  Consejo Superior de Investigaciones Cientificas (CSIC) in Granada,  Spain, to develop a simplified genetic-based nomenclature that  automatically catalogues the entire RF gene products into families and  subfamilies.
"Up to now, there has been no unified nomenclature for naming the RF  proteins," Seufferheld said. "As the systematic sequencing of new plant  species has increased in recent years, naming has been simply  arbitrary. We have had 'chaos' in the databases. The RF information in  the databases could not be adequately handled in the context of  comparative functional genomics."
This new tool will help plant breeders and scientists make decisions  more quickly. Breeders can now easily match sterility in plants to male  restorer mechanisms. Ultimately, growers may benefit sooner from new  developments in plant breeding since breeders will be able to generate  new hybrids at a faster pace, Jimenez-Lopez said.
"Genomic sequencing, coupled with protein modeling, allowed us to  begin dismantling this complexity that has held us back in the field of  science," Kotchoni said. "Now we can easily compare unknown gene  functions to known and well characterized genes in order to determine  their functions and family hood."
With many teams of researchers competing to finish this task first,  Kotchoni said it has been an honor to have this model accepted as the  new standard for RF protein nomenclature. This system has been developed  as a building block for plant genomics.
"The nomenclature, which is designed to include new RF genes as they  become available in the future, is not based on one species or another,  but rather on the function of the gene itself," Seufferheld said. "This  allows scientists to work with a wide range of plants and take a gene  with known function(s) from one plant and transfer it into another plant  to restore male fertility."
Corn growers only need to look back to the southern corn leaf blight  epidemic in 1972 to see the importance of this scientific development.
In 1972, Texas-Cytoplasm Male Sterility (T-CMS) corn was heavily  used in hybrid seed production because it eliminated the costly practice  of hand detasseling. Nearly 85 percent of the U.S. corn crop was  produced using T-CMS, which was highly susceptible to Helminthosporium  maydis, the fungus that causes southern corn leaf blight.
Since then, understanding the function of RF genes in higher plants  has been a priority of many researchers. "The first male sterility  restorer ever characterized in plants was maize ALDH," Kotchoni said.  "When this gene is altered, it causes male sterility."
Seufferheld said this will also be a great tool for studying plant evolution.
"We can follow how plants became domesticated," Seufferheld said.  "It is easier now because we have all the structures of the RF proteins  organized and can look at the evolution of these proteins in a  systematic manner. If we just look at the sequence of the gene, part of  the phylogenetic scene has been lost through evolution. However, the  structure of protein provides more information that can go well into the  past."
This public gene database will allow scientists to search using the old or new names of RF proteins, Seufferheld said.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6418</link><pubDate>Wed, 05 Jan 2011 03:48:00 PDT</pubDate></item><item><title>New technology improves greenhouse, plant microclimates</title><description>A study in &lt;em&gt;HortTechnology&lt;/em&gt; featured a new technology that  improved greenhouse climates by reducing solar heat radiation and  temperatures during the hot summer season. The study, published by a  team of Canadian researchers, was the first investigation into the  effects of application of the liquid foam technology as a shading  method. Results showed that the technology improved greenhouse and plant  microclimates and decreased air temperature more than conventional  shading curtains traditionally used by greenhouse growers.
Excess temperature, solar radiation, and high vapor pressure deficit  are major greenhouse concerns during the summer season. These extreme  conditions increase plant stress and decrease crop productivity and  fruit quality. Methods such as cooling pads and fogging systems have  been used to prevent plant heat stress during the day, and various  shading techniques are often used by growers to decrease solar radiation  and reduce air and leaf temperatures. Shade cloths reduce the amount of  solar energy entering the greenhouse and consequently decreased air  temperature by partially cutting the heat portion of the solar  radiation, but this incoming energy usually contains more than 50% heat  (infrared radiation), which is not useful for plant growth in the  summer.
Sunarc of Canada, Inc. developed an innovative new shading  technology that generates retractable liquid foam and distributes it  between two layers of polyethylene film used as a greenhouse covering  material. The Canadian research team set out to determine the effects of  different shading strategies using the liquid foam technology on  greenhouse and plant microclimates. The research was conducted over 2  years in two different areas of Canada, where experimental greenhouses  were retrofitted with the new technology. Tomato and sweet pepper plants  were used with two shading strategies: a conventional nonmovable  shading curtain compared to the liquid foam shading system based only on  outside global solar radiation, and foam shading applications based on  both outside global solar radiation and greenhouse air temperature. The  team recorded data on the greenhouse microclimate (global solar  radiation, air temperature, and relative humidity), the canopy  microclimate (leaf and bottom fruit temperatures), and ventilation  (opening/closing).
"This study showed that the retractable liquid foam technology  improved greenhouse climate", noted Kamal Aberkani, lead author of the  report. "Under very sunny, very hot conditions, a difference of up to 6  &amp;ordm;C in air temperature was noted between the unshaded and shaded  greenhouses as a result of liquid foam application at 40-65% shading."
According to the report, additional benefits of the technology  included an increase of up to 12% in greenhouse relative humidity, a  decrease in the frequency of roof ventilation operation, and an increase  in the length of time bottom fruit temperature remained cool after  shading ended.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6383</link><pubDate>Wed, 29 Dec 2010 03:21:31 PDT</pubDate></item><item><title>K-State research looks at pathogenic attacks on host plants</title><description>Two Kansas State University researchers focusing on rice genetics are  providing a better understanding of how pathogens take over a plant's  nutrients.
Their research provides insight into ways of reducing crop losses or developing new avenues for medicinal research.
Frank White, professor of plant pathology, and Ginny  Antony, postdoctoral fellow in plant pathology, are co-authors, in  partnership with researchers at three other institutions, of an article  in a recent issue of the journal Nature. The article, "Sugar  transporters for intercellular exchange and nutrition of pathogens," was  led by Li-Qing Chen from the department of plant biology in the  Carnegie Institution for Science at Stanford University.
The project involves the identification a family of sugar  transporters, called SWEETS, which transport glucose between plant  cells. These transporters are also important because they are targeted  by pathogens trying to obtain plant sugar for nutrition......&amp;gt; &lt;a href="http://www.k-state.edu/media/newsreleases/dec10/sugartransporters121710.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6323</link><pubDate>Mon, 20 Dec 2010 03:27:54 PDT</pubDate></item><item><title>Study shows garlic could protect against hip osteoarthritis</title><description>Researchers at King's College London and the University of East  Anglia have discovered that women who consume a diet high in allium  vegetables, such as garlic, onions and leeks, have lower levels of hip  osteoarthritis.
The findings, published in the &lt;em&gt;BMC Musculoskeletal Disorders&lt;/em&gt; journal, not only highlight the possible effects of diet in protecting  against osteoarthritis, but also show the potential for using compounds  found in garlic to develop treatments for the condition.
A relationship between body weight and osteoarthritis was previously  recognised, although it is not yet completely understood. This study is  the first of its kind to delve deeper into the dietary patterns and  influences that could impact on development and prevention of the  condition.
Osteoarthritis is the most common form of arthritis in adults,  affecting around 8 million people in the UK, and women are more likely  to develop it than men. It causes pain and disability by affecting the  hip, knees and spine in the middle-aged and elderly population.  Currently there is no effective treatment other than pain relief and,  ultimately, joint replacement.
The study, funded by Arthritis Research UK, the Wellcome Trust and  Dunhill Medical Trust, looked at over 1,000 healthy female twins, many  of whom had no symptoms of arthritis.
The team carried out a detailed assessment of the diet patterns of  the twins and analysed these alongside x-ray images, which captured the  extent of early osteoarthritis in the participants' hips, knees and  spine.
They found that in those who consumed a healthy diet with a high  intake of fruit and vegetables, particularly alliums such as garlic,  there was less evidence of early osteoarthritis in the hip joint.
To investigate the potential protective effect of alliums further,  researchers studied the compounds found in garlic. They found that that a  compound called diallyl disulphide limits the amount of  cartilage-damaging enzymes when introduced to a human cartilage  cell-line in the laboratory.
Dr Frances Williams, lead author from the Department of Twin  Research at King's College London, says: "While we don't yet know if  eating garlic will lead to high levels of this component in the joint,  these findings may point the way towards future treatments and  prevention of hip osteoarthritis.
"It has been known for a long time that there is a link between body  weight and osteoarthritis. Many researchers have tried to find dietary  components influencing the condition, but this is the first large scale  study of diet in twins. If our results are confirmed by follow-up  studies, this will point the way towards dietary intervention or  targeted drug therapy for people with osteoarthritis."
Professor Ian Clark of the University of East Anglia said:  "Osteoarthritis is a major health issue and this exciting study shows  the potential for diet to influence the course of the disease.  With  further work to confirm and extend these early findings, this may open  up the possibility of using diet or dietary supplements in the future  treatment osteoarthritis."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6313</link><pubDate>Fri, 17 Dec 2010 03:46:13 PDT</pubDate></item><item><title>Scientists unravel more details of plant cell-wall construction</title><description>One big challenge in converting plants to biofuels is that the very  same molecules that keep plants standing up make it hard to break them  down. Now scientists at the U.S. Department of Energy's (DOE) Brookhaven  National Laboratory are unraveling details of how plant cells'  structural supports - their cell walls - are made, with the hope of  finding ways to change their composition for more efficient biofuel  production.
In a paper to be published the week of December 13, 2010, in the &lt;em&gt;Proceedings of the National Academy of Sciences&lt;/em&gt;,  the researchers describe details of how precursors to lignin, one  important cell-wall component, are transported across cellular membranes  prior to linking up. The key finding, that the process requires a class  of energy-dependent transporter molecules, may provide a "chink in the  armor" that opens a way to alter plants' lignin content.
"Being able to manipulate lignin biosynthesis would have a great  influence on our ability to produce renewable biofuels from plant  cellulosic feedstocks, and could also have a large effect on many other  agricultural and industrial processes, such as the production of paper  and more digestible foods for grazing animals," said lead author  Chang-Jun Liu, a Brookhaven biologist.
Prior to cell-wall construction, lignin precursors known as  monolignols are made in the cell's interior cytoplasm. Some precursors  may be sequestered in internal vacuoles for storage, while some move out  of the cell to link up and form the lignin component of the cell wall -  a protective and supportive barrier around the cell. In both cases, the  precursors move across a membrane, either out of the cell or into the  vacuole. But no one was certain how the process occurred - whether by  simple diffusion or via some active transport mechanism.
The Brookhaven team unraveled the mystery by isolating portions of  cellular and vacuolar membrane from Arabidopsis and poplar plants,  making them into closed vesicles that resemble bubbles, and mixing in  pure monolignols and ones that have been chemically modified to form  monolignol glucosides, which are commonly observed in some plants. They  then monitored which type and how much of each precursor moved across  the two kinds of membranes and into the vesicles under a range of  conditions, including in the presence of inhibitors for different kinds  of transport molecules.
The range of assays revealed that pure monolignols move across the  cellular membrane while monolignol glucosides move preferentially into  vacuoles. But most importantly, very little of either precursor would  move across either type of membrane without the addition of ATP, the  molecular "currency" for energy in cells.
"ATP is the energy molecule that is well known for providing the  driving force for a group of transporters called ATP-binding cassette  (ABC) transporters on cell membranes," Liu said.
To prove the point, adding an agent that specifically inhibits ABC  transporters completely blocked uptake of lignin precursors by both  types of membrane vesicles.
With these experiments and additional evidence, Liu and his  colleagues demonstrated that ABC-like transporters on cell membranes are  responsible for the transport of lignin precursors.
Now that the scientists have identified a class of transporters  likely involved in sequestering and transporting lignin's building  blocks, they'll pursue detailed studies to identify exactly which  members of the class are involved.
"If we can identify those particular transporters we might be able  to control their expression to reduce the precursor deposited into the  cell wall, and thus lower the cell-wall content of lignin -or,  selectively control the particular type of precursor deposited to change  lignin composition and produce more easily cleavable biopolymers," Liu  said.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6284</link><pubDate>Tue, 14 Dec 2010 03:26:31 PDT</pubDate></item><item><title>Plant disease 'stealth bomber' tactics subverted to tackle hundreds of plant pathogens</title><description>Research, led by the University of Warwick, The Sainsbury Laboratory,  and Virginia Polytechnic Institute and State University (Virginia  Tech), has sequenced the genome of a plant disease causing organism  revealing that it acts like a "stealth bomber of plant pathogens". The  research has uncovered the tactics used to sneak past the plant's immune  defences. That same discovery also provides tools for researchers to  identify the components of the plant immune system and devise new ways  to prevent disease.
The research at the University of Warwick, the Sainsbury Laboratory  and Virginia Tech, was funded by the UK's Biotechnology and Biological  Sciences Research Council (BBSRC), The Gatsby Charitable Foundation,  NSF, and the U.S. Department of Agriculture. It looked at an obligate  biotroph, a type of plant pathogen which has adapted so exquisitely to  its host that it extracts nutrients only from living plant tissue and  cannot grow away for their plant. While the organism may once have been  able to exist by itself it has now evolved in such a way that it cannot  survive without a host plant and usually that has to be a very specific  type of host plant.
The researchers looked specifically at &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt;, that can only survive on its host the model plant &lt;em&gt;Arabidopsidis&lt;/em&gt;,  the model plant  of the plant science world. Hyaloperonospora  arabidopsis is a type of water mould that causes yellow patches and  fuzzy white mould on the leaves. Close relatives cause disease and  damage on many crops including broccoli, maize, grapes and lettuce. The  researchers found that this particular plant pathogen has evolved a  highly successful strategy that allows it to present a very small  profile to its host plant disease prevention defences. By losing, or  never acquiring in the first place, many abilities found in other  pathogens, &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; is able to minimise the  number of genetic markers it carries that could be picked up by a  plant's defences and seen as a threat.
The lead researcher from the University of Warwick's School of Life Sciences Professor Beynon said:
"&lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; is one of the stealth bombers  of the world of plant pathogens.  We can see much of how it has  actually slimmed down some key elements of its genetic material in order  to get around the plant's natural defences - essentially by stealth."
One of the key ways the University of Warwick, Sainsbury Laboratory  and Virginia Tech researchers will exploit this plant pathogen's arsenal  to mount their own sneak assault on many much other challenging plant  pathogens is through the "RXLR effectors". Such pathogens use a large  armoury  of "RXLR effectors" to suppress the mechanisms used by plants  to detect and then block pathogens. Although having a slimmed down  stealth profile &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; still maintains an  amazing 134 RXLR effectors in its armoury. Understanding the role of  these effectors will be the key direction of future research in the  field.
This parsimonious approach may help &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; in its stealth attack but it also opens up a major opportunity for  researchers to gain insights across a vast range of plant pathogens. Not  only does &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; infect the ideal plant  model (Arabidopsis) used by plant researchers the world over for decades  &amp;ndash; it also attacks that model plant with a bare bones set of weapons  that greatly simplifies a researcher's task in unpicking how those  weapons work. Any insights gained can then be directly applied to the  understanding of how those same weapons work in much more complicated  pathogens.
Professor Beynon also said:
"This research provides a new window into how &lt;em&gt;Hyaloperonospora arabidopsidis&lt;/em&gt; has slimmed down key elements of its genetic material to avoid the  plant's natural defences. Despite this reduction, amazingly, it still  sends over 100 proteins into plant cells to suppress the immune  responses. Understanding how these proteins suppress plant immunity will  enable us to select disease resistant crop plants and combat plant  disease such as potato blight and sudden oak death."
"Losses to disease in food crops can be very significant and to feed a  growing population set to reach 9 billion by 2050 we need to increase  food production. Reducing losses because of disease will be an important  part of this."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6261</link><pubDate>Fri, 10 Dec 2010 03:19:11 PDT</pubDate></item><item><title>New discovery about how flowering time of plants can be controlled</title><description>Researchers at Ume&amp;aring; Plant Science Center in Sweden discovered, in  collaboration with the Syngenta company, a previously unknown gene in  sugar beets that blocks flowering. Only with the cold of winter is the  gene shut off, allowing the sugar beet to blossom in its second year.  The discovery of this new gene function makes it possible to control  when sugar beets bloom. The new findings were recently published in the  prestigious journal &lt;em&gt;Science&lt;/em&gt;.
Scientists at Ume&amp;aring; Plant Science Center and the international  company Syngenta, in a joint study of genetic regulation in the sugar  beet, have discovered an entirely new principle for how flowering can be  controlled. The study, which was co-directed by Professorn Ove Nilsson,  of the Swedish University of Agricultural Sciences (SLU), and Syngenta  scientist Dr. Thomas Kraft, showed that there is a gene in the sugar  beet that was previously unknown.
"When we studied a gene in the sugar beet that usually stimulates  blooming in other plants, we made a very surprising discovery: in the  sugar beet evolution has developed a 'sister gene' that has taken on the  exact opposite function, namely, to inhibit blossoming. For biennial  sugar beets this means that they can't flower in their first year. Once  the plants have been exposed to the cold of winter at the end of the  first year, the 'gene blockade is lifted,' and the sugar beets can bloom  in their second year of life," says Ove Nilsson about the function of  the newly discovered flowering gene.
The researchers speculate that the development of the inhibiting  sister gene was an important factor in enabling biennial sugar beets to  evolve from an annual to a biennial plant. Furthermore, plant  researchers in Ume&amp;aring; and Landskrona have shown that it is possible to  manipulate the "flowering gene" in such a way as to leave the gene  constantly "turned on," that is, to block blooming, and thereby prevent  it from being turned off after winter.
"In that way it's possible to fully control the flowering time of  the sugar beet. This enables us to develop a so-called 'winter beet,'  that is, a sugar beet that can be planted in the autumn and then will  continue to grow throughout the following growth season without  blossoming," says Thomas Kraft at Syngenta Seeds.
"A winter beet has be a high priority for sugar beet growers, since  it is estimated to be able to increase the yield by about 25 percent and  at the same time allow a more extended harvesting period. Traditional  breeding has failed to produce such a plant. Syngenta Seeds is now going  to move on to more in-depth tests of this potential new winter beet."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6245</link><pubDate>Wed, 08 Dec 2010 03:30:09 PDT</pubDate></item><item><title>Gene discovery suggests way to engineer fast-growing plants</title><description>Tinkering with a single gene may give perennial grasses more robust  roots and speed up the timeline for creating biofuels, according to  researchers at the Duke Institute for Genome Sciences &amp;amp; Policy  (IGSP).
Perennial grasses, including switchgrass and miscanthus, are  important biofuels crops and can be harvested repeatedly, just like lawn  grass, said Philip Benfey, director of the IGSP Center for Systems  Biology. But before that can happen, the root system needs time to get  established.
"These biofuel crops usually can't be harvested until the second or  third year," Benfey said. "A method to improve root growth could have a  major role in reducing the time to harvest for warm season grasses."
Benfey's team appears to have found a way to do just that. They took  a directed genomic approach aimed at identifying genes that become  active when cells stop dividing and start taking on the characteristics  of the mature, adult cell they are to become. "We systematically looked  for those genes that come 'on' precisely when cells transition from  proliferation to differentiation and then turn 'off' again just as  quickly," Benfey said.
That genome-wide search in the roots of the familiar laboratory  plant Arabidopsis and subsequent screening of mutant lines turned up a  single gene, which the researchers call UPBEAT1 (UPB1). Further study  showed that UPB1 controls the gene expression of enzymes known as  peroxidases.
They then showed that these peroxidases control the balance of free  radicals between the zone of cell proliferation and the zone of cell  elongation where differentiation begins. (Although free radicals are  probably most familiar as agents of stress to be combated with  antioxidants, Benfey noted that the balance of free radicals has also  been implicated in the control of a similar transition from  proliferation to differentiation in animals.)
When the researchers experimentally disrupted UPB1 activity in the  plant root, it altered the balance of free radicals such that cells  delayed their differentiation and continued growing. Those plants ended  up with faster-growing roots, having more and larger cells. When UPB1  activity was artificially increased, the growth of plant roots slowed.
"It's possible that by manipulating a single gene, you could get a  plant with rapid growth," Benfey said. Interestingly, UPB1 appears to  act independently of plant hormones that play well-known roles in the  balance between cell division and differentiation.
From an engineering perspective, the prospect of enhancing growth by  taking a gene away, as opposed to adding one, is particularly  appealing, Benfey notes.
"It also suggests that plants are not growing at their full  potential," he says. That makes sense, of course, as plants in the real  world have to make tradeoffs, for example, between growth and  reproduction.
In addition to their potential in biofuels production, the findings  might also lead to new ways to produce bigger and stronger plants with  the capacity to sequester more earth-warming carbon dioxide from the  atmosphere, Benfey says. His startup company, GrassRoots Biotechnology  Inc., has acquired the patent for this discovery with its potential in  mind. The company's primary goals are the development of next-generation  biofuels and the use of root systems for carbon sequestration.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6069</link><pubDate>Fri, 12 Nov 2010 03:24:54 PDT</pubDate></item><item><title>To prevent inbreeding, flowering plants have evolved multiple genes, research reveals</title><description>A research team led by Teh-hui Kao, professor of biochemistry and  molecular biology at Penn State University, in collaboration with a team  lead by Professor Seiji Takayama at the Nara Institute of Science and  Technology in Japan, has discovered a large suite of genes in the  petunia plant that acts to prevent it from breeding with itself or with  its close relatives, and to promote breeding with unrelated individuals.  In much the same way that human inbreeding sometimes results in genetic  disease and inferior health, some inbred plants also experience  decreased fitness, and therefore, have developed mechanisms to ensure  that their offspring benefit from hybrid vigor -- the mix that results  when genetically distinct members of the same species breed. The team's  discovery of the multiple inbreeding-prevention genes will be published  on 5 November 2010 in the journal &lt;em&gt;Science&lt;/em&gt;. The identification of  these genes comes on the heels of Kao's earlier identification of two  additional inbreeding-prevention genes in the same plant.
"Humans have mechanisms to prevent inbreeding that are in part  cultural," Kao explained. "But a plant can't just get up and move to the  next town to find a suitable, unrelated mate. Some other system must be  at work." Kao began to unravel the mystery of what he calls a "non-self  recognition system" in the mid 1980s by studying the genetic sequence  of petunias. Petunias and many common garden plants are hermaphroditic,  possessing both male and female reproductive organs, and these  reproductive organs are located in close proximity in the same flower.  This floral anatomy makes it easy for a plant's pollen to land on  itself, resulting in self-fertilization and genetically inferior, inbred  offspring. To prevent self-fertilization, many flowering plants,  including the petunia, have evolved a strategy called  self-incompatibility, or the ability to recognize self and non-self  components within both the male and female reproductive organs.
&lt;strong&gt;PRIOR RESEARCH&lt;/strong&gt;
Because of the petunia's hermaphroditic nature, Kao and his  colleagues assumed that there had to be both male and female genetic  strategies to prevent a plant from breeding with itself or with close  relatives. In 1994, Kao's team discovered the first piece of the  self-incompatibility puzzle. In a paper published in Nature, he and his  colleagues announced that they had identified a gene called S-RNase (S  for self-incompatibility) in Petunia inflata, a wild relative of the  garden petunia. The S-RNase gene controls self-incompatibility in the  pistil -- the plant's female reproductive organ. Thanks to this gene,  the pistil is able to distinguish between self and non-self pollen,  which is analogous to sperm cells, and specifically kills self-pollen to  prevent inbreeding. Later, in another paper published in Nature in  2004, Kao's team announced the discovery of the male counterpart of  S-RNase -- a gene called Type-1 SLF -- that controls  self-incompatibility in pollen by distinguishing between self and  non-self pistil S-RNase proteins, and specifically detoxifying non-self  S-RNase proteins, thereby allowing outcrossing.
That is, the team found that the S-RNase and the Type-1 SLF genes  worked in concert to control the way in which the plant accepted or  disallowed the introduction of particular pollen into its own  reproductive system. In summary, they found that, thanks to the genetic  interaction between the male-component and female-component genes, a  plant pollinated by its own pollen or by pollen of a similar genotype  failed to produce seeds. However, a plant pollinated by pollen of a  sufficiently distinct genotype produced seeds and reproduced  successfully.
More recently, Kao and his colleagues set out to fill in some  important missing pieces in the self-incompatibility puzzle. "During  previous research studies, other researchers who had studied the  evolutionary histories of Type-1 SLF and S-RNase found no evidence of  co-evolution, which was surprising as the male and female genes directly  involved in controlling self/non-self recognition during sexual  reproduction are expected to have co-evolved." Kao said. "In fact,  Type-1 SLF has a much shorter evolutionary history than S-RNase."  Meanwhile, Kao and his team noticed that "Type-1 SLF had a much lower  allelic sequence diversity when compared to S-RNase, raising a question  as to how, with limited allelic diversity, the allelic variants of  Type-1 SLF proteins can recognize a large repertoire of 40 or more  highly divergent S-RNase proteins," he said. "We were puzzled by how the  Type-1 SLF gene seemed to have such a young evolutionary history, and  how the allelic variants of Type-1 SLF protein seemed to have such a low  sequence diversity. We knew that the male and female genetic  counterparts had to have kept up with each other throughout evolution --  they had to have co-evolved -- so that meant there had to be older and  more numerous SLF genes controlling the male side of the equation."
&lt;strong&gt;NEW DISCOVERIES&lt;/strong&gt;
Now, in the soon-to-be-published Science paper, the team will  announce its identification of five additional types of SLF genes --  named Type-2 to Type-6 SLF genes -- found in the same chromosomal region  as the Type-1 SLF gene. Kao and his colleagues found that while the  Type-1 SLF gene certainly played an important role in preventing  inbreeding, Type-2 and Type-3, and most likely additional types of SLF  genes, also controlled self-incompatibility. "Each Type-1 SLF protein  can recognize only a limited number of non-self S-RNase components," Kao  said. "Meanwhile, each of the additional types of SLF proteins we've  found can recognize different sets of non-self S-RNase proteins, and all  of them collectively account for the entire suite of non-self  identification. This recent finding has solved the puzzle about the  co-evolution between the male and female genes, and how a single type of  SLF protein has the capacity to recognize a large number of highly  divergent S-RNase proteins."
Kao also explained that self-incompatibility in plants can be  likened to the adaptive immune system in vertebrates. "The plant needs  to distinguish between non-self and self to know which plants it should  breed with and which it should reject as too similar," Kao explained.  "In the same way, our bodies distinguish between non-self and self to  know what to attack and what to leave alone." Kao explained that when  pathogens enter our bodies, our T-cells recognize them as foreign  invaders and battle against them by triggering production of antibodies  by B-cells. "When this system goes awry, our bodies misidentify self as  non-self and attack it," Kao said. "These attacks on our own tissues are  known as auto-immune disorders; arthritis and Lupus are just a couple  of examples." Kao also explained that, just as we have evolved many  different types of T-cell receptors to collectively recognize the many  foreign antigens we might encounter in our environment, plants have  evolved many versions of self-incompatibility genes that produce  multiple types of SLF proteins in pollen to collectively recognize a  large suite of possible non-self elements -- S-RNase proteins.
In addition to Kao, other members of the research team include  Ken-ichi Kubo, Tetsuyuki Entani, Akie Takara, Mamiko Toyoda, Shin-ichi  Kawashima, Akira Isogai, and Seiji Takayama from Japan's Nara Institute  of Science and Technology; Ning Wang, Allison M. Fields, and Zhihua Hua  from Penn State; and Toshio Ando from Japan's Chiba University. The  research conducted at Penn State was funded by the National Science  Foundation.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=6023</link><pubDate>Fri, 05 Nov 2010 03:36:48 PDT</pubDate></item><item><title>Researchers could use plant's light switch to control cells</title><description>Chandra Tucker shines a blue light on yeast and mammalian cells in  her Duke University lab and the edges of them start to glow. The effect  is the result of a light-activated switch from a plant that has been  inserted into the cell.
Researchers could use this novel "on-off switch" to control cell  growth or death, grow new tissue or deliver doses of medication directly  to diseased cells, said Tucker, an assistant research professor in the  biology department at Duke.
She and colleagues created the switch by genetically inserting two proteins from a mustard plant, &lt;em&gt;Arabidopsis thaliana&lt;/em&gt;,  into yeast cells, kidney cells and cultured rodent brain tissue. The  two proteins interact under light to provide the control over cell  functions.
The switch is similar to one described last year where researchers  genetically inserted a different light-receptive plant protein and its  interacting protein partner from &lt;em&gt;Arabidopsis&lt;/em&gt; into mammalian  cells. In response to red light, these proteins interacted to cause  mammalian cells to change shape, moving in the direction of the light.
Tucker's switch uses &lt;em&gt;Arabidopsis&lt;/em&gt; proteins that respond to  blue light. Unlike the red-light activated proteins, which need an added  cofactor, a chemical that is required for the light response, the  blue-light switch doesn't need any additional chemicals to work because  it uses a cofactor that naturally exists in non-plant organisms.
"It's hard to deliver a chemical to a fly or to individual cells.  This new approach, with one of the molecules already in the mammalian or  yeast cells, makes building a light-controlled switch a lot easier,"  Tucker said. Her team describes the switch in the Oct. 31 &lt;em&gt;Nature Methods&lt;/em&gt;.
To test the switch, the team fused one of the light-sensitive &lt;em&gt;Arabidopsis&lt;/em&gt; proteins to a red fluorescent protein and the other to a green  fluorescent protein, which was in turn attached to the cell membrane.  When the researchers flashed blue light on the cell, the plant proteins  interacted, causing the red fluorescent protein to rapidly move to the  cell membrane, which then glowed yellow due to the merging of the red  and green fluorescing proteins. The team found that this interaction was  reversible and could be triggered repeatedly with light exposure.
The switch is one among several that have been designed to give  researchers better control of different functions of the cell. The next  step in developing the switch will be to make the interacting proteins  more effective, Tucker said. The approach is expected to be applicable  not only for studies in cultured cells and yeast, but also worms, fruit  flies, mice and other model organisms. Eventually this method could  allow researchers to test how cells in a tissue affect neighboring cells  in a tissue, to guide axon growth in neurons to repair brain tissue, or  even to kill cancer cells.
Tucker's new approach will be a "major boon" to those who wish to  apply light activation to their own experimental systems, said Klaus  Hahn, a pharmacologist at the University of North Carolina at Chapel  Hill, whose lab reported on another blue-light responsive protein to  control movement of mammalian cells last year.
Hahn said the "elegant work will likely see broad use, in many  fields and for applications that will surprise us," and it is already  going to be applied to important areas of research, such as control of  gene expression.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5978</link><pubDate>Mon, 01 Nov 2010 03:22:18 PDT</pubDate></item><item><title>Transgenic corn suppresses European corn borer, saves farmers billions</title><description>Transgenic corn's suppression of the European corn borer has saved  Midwest farmers billions of dollars in the past decade, reports a new  study in &lt;em&gt;Science&lt;/em&gt;.
Research conducted by several Midwest universities shows that  suppression of this pest has saved $3.2 billion for corn growers in  Illinois, Minnesota, and Wisconsin over the past 14 years with more than  $2.4 billion of this total benefiting non-Bt corn growers. Comparable  estimates for Iowa and Nebraska are $3.6 billion in total, with $1.9  billion accruing for non-Bt corn growers.
Transgenic corn is engineered to express insecticidal proteins from  the bacterium Bacillus thuringiensis (Bt). Bt corn has become widely  adopted in U.S. agriculture since its commercialization in 1996. In  2009, Bt corn constituted 63 percent of the U.S. crop.
Corn borer moths can't distinguish between Bt and non-Bt corn, so  females lay eggs in both types of fields. Once eggs hatch in Bt corn,  young borer larvae feed and die within 24 to 48 hours.
The major benefit of planting Bt corn is reduced yield losses, and  Bt acres received this benefit after the growers paid Bt corn technology  fees. But as a result of areawide pest suppression, non-Bt acres also  experienced yield savings without the cost of Bt technology fees, and  thus received more than half of the benefits from growing Bt corn in the  region.
"We've assumed for some time that economic benefits were accruing,  even among producers who opted not to plant Bt hybrids," said co-author  of the study Mike Gray, University of Illinois Extension entomologist  and professor in the Department of Crop Sciences. "However, once  quantified, the magnitude of this benefit was even more impressive."
Over the past several years, entomologists and corn producers have  noticed very low densities of European corn borers in Illinois. In fact,  Illinois densities have reached historic lows to the point where many  are questioning its pest status, Gray said.
"Since the introduction of Bt corn, initially targeted primarily at  the European corn borer, many entomologists and ecologists have wondered  if population suppression over a large area would eventually occur,"  Gray said. "As this research shows, areawide suppression has occurred  and dramatically reduced the estimated $1 billion in annual losses  caused previously by the European corn borer."
This information also provides incentives for growers to plant non-Bt corn in addition to Bt corn.
"Sustained economic and environmental benefits of this technology  will depend on continued stewardship by producers to maintain non-Bt  maize refuges to minimize the risk of evolution of Bt resistance in crop  pest species," Gray said.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5783</link><pubDate>Fri, 08 Oct 2010 03:24:02 PDT</pubDate></item><item><title>Ecologists find new clues on climate change in 150-year-old pressed plants</title><description>Plants picked up to 150 years ago by Victorian collectors and held by  the million in herbarium collections across the world could become a  powerful &amp;ndash; and much needed &amp;ndash; new source of data for studying climate  change, according to research published this week in the British  Ecological Society's &lt;em&gt;Journal of Ecology&lt;/em&gt;.
The scarcity of reliable long-term data on phenology &amp;ndash; the study of  natural climate-driven events such as the timing of trees coming into  leaf or plants flowering each spring &amp;ndash; has hindered scientists'  understanding of how species respond to climate change.
But new research by a team of ecologists from the University of East  Anglia (UEA), the University of Kent, the University of Sussex and the  Royal Botanic Gardens, Kew shows that plants pressed up to 150 years ago  tell the same story about warmer springs resulting in earlier flowering  as field-based observations of flowering made much more recently.
The team examined 77 specimens of the early spider orchid (&lt;em&gt;Ophrys sphegodes&lt;/em&gt;)  collected between 1848 and 1958 and held at the Royal Botanic Gardens,  Kew and the Natural History Museum in London. Because each specimen  contains details of when and where it was picked, the researchers were  able to match this with Meteorological Office records to examine how  mean spring temperatures affected the orchids' flowering.
They then compared these data with field observations of peak  flowering of the same orchid species in the Castle Hill National Nature  Reserve, East Sussex from 1975 to 2006, and found that the response of  flowering time to temperature was identical both in herbarium specimens  and field data. In both the pressed plants and the field observations,  the orchid flowered 6 days earlier for every 1oC rise in mean spring  temperature.
The results are first direct proof that pressed plants in herbarium  collections can be used to study relationships between phenology and  climate change when field-based data are not available, as is almost  always the case.
According to the study's lead author, PhD student Karen Robbirt of  UEA: "The results of our study are exciting because the flowering  response to spring temperature was so strikingly close in the two  independent sources of data. This suggests that pressed plant  collections may provide valuable additional information for  climate-change studies."
"We found that the flowering response to spring temperature has  remained constant, despite the accelerated increase in temperatures  since the 1970s. This gives us some confidence in our ability to predict  the effects of further warming on flowering times."
The study opens up important new uses for the 2.5 billion plant and  animal specimens held in natural history collections in museums and  herbaria. Some specimens date back to the time of Linnaeus (who devised  our system of naming plants and animals) 250 years ago.
Co-author Professor Anthony Davy of UEA says: "There is an enormous  wealth of untapped information locked within our museums and herbaria  that can contribute to our ability to predict the effects of future  climate change on many plant species. Importantly it may well be  possible to extend similar principles to museum collections of insects  and animals."
Phenology &amp;ndash; or the timing of natural events &amp;ndash; is an important means of  studying the impact of climate change on plants and animals.
"Recent climate change has undoubtedly affected the timing of  development and seasonal events in many groups of organisms.  Understanding the effects of recent climate change is a vital step  towards predicting the consequences of future change. But only by  elucidating the responses of individual species will we be able to  predict the potentially disruptive effects of accelerating climate  change on species interactions," he says.
Detecting phenological trends in relation to long-term climate  change is not straightforward and relies on scarce long-term studies.  "We need information collected over a long period to enable us  confidently to identify trends that could be due to climate change.  Unfortunately most field studies are relatively brief, so there are very  few long-term field data available," Professor Davy explains</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5644</link><pubDate>Wed, 22 Sep 2010 03:21:58 PDT</pubDate></item><item><title>AgriLife research hibiscus breeder comes up with the blue</title><description>Dr. Dariusz Malinowski is seeing blue, and he is very excited.
For four years, Malinowski, an AgriLife Research plant  physiologist and forage agronomist in Vernon, has been working with  collaborators Steve Brown of the Texas Foundation Seed and Dr. William  Pinchak and Shane Martin with AgriLife Research on a winter-hardy  hibiscus breeding project.
The project was first a private hobby of the inventors and  became a part of the strategic plan of the Texas AgriLife Research and  Extension Center at Vernon in 2009. The flower commercialization is a  part of the research on non-traditional or under-utilized crops that  have value because of drought tolerance.
Malinowski's breeding goal has been to create a blue-flowering winter-hardy hibiscus.
"A blue pigment does not exist in this species, thus hybridizers  have not been successful so far in creating a plant with blue flowers,"  he said. "There are a couple of recently introduced cultivars with plum  and lavender flower color."
But now Malinowski has managed to breed a flower with the illusive color.
He and his collaborators have created a number of lines with  unique flower and foliage shape and color. The new hibiscus hybrids  range in color from white through different shades of pink, lavender,  bluish, red and magenta tones, and some of them have combinations of two  or even three colors.
One line has dark maroon foliage with moderately big, white  flowers that blend into a pink center with darker veins, Malinowski  said. Flower size of these hybrids varies from miniature blooms 2 inches  in diameter to the size of dinner plates, about 12 inches in diameter.
Malinowski has been using these cultivars in his breeding  project for several generations. This year, they finally had one plant  bloom with almost blue flowers, a significant breakthrough in efforts to  create a blue hibiscus cultivar.
"It took four years of work and more than 1,000 crosses among  three winter-hardy hibiscus species to achieve this goal of creating an  almost-blue flowering hibiscus hybrid," he said.     The new hybrid is not perfect yet, Malinowski said.
"The flowers get a fantastic blue hue in shade, but in full sunlight they are still plum-lavender-bluish," he said.
Brown said it is important to note that in the world of  ornamentals, "blue" is interpreted to have a wide range of hues. Most  ornamental blues have a more purple or lavender cast.
"There are very few true blue flowers in any ornamental  cultivar," he said. "Although I would call this flower 'almost blue' as  Dariusz has, there is no question that this development is unique in  known hardy hibiscus color ranges.
"My expectation is that we will see more vibrant colors in next  year's F1s (cultivars) using this line as a parent," Brown said.
Malinowski said he will use this plant as a parent in his  breeding project this summer, with the goal to stabilize the blue color  in full sunlight and increase flower size from the current 7 inches to  the "magic" 12-inch diameter.
Breeding of ornamental plants is not the major research area of  Malinowski, but he said he enjoys new challenges and the benefits of  combining his private hobby with business.
"I never thought I would be an expert in breeding winter-hardy  hibiscus," he said. "The knowledge I have gained during the past few  years of intensive work on hardy hibiscus helps me reach most of the  breeding objectives in a relatively short time."
What is next? Malinowski and his collaborators have a new challenge - to create an orange flowering hardy hibiscus.
This goal seems to be even more difficult, but not impossible,  Malinowski said. It will require hybridization with a distantly related  hibiscus species, which has shades of orange flowers. The researchers  hope that with the help of molecular genetic tools they will be able to  meet this objective.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5495</link><pubDate>Sat, 04 Sep 2010 04:16:36 PDT</pubDate></item><item><title>Core knowledge of tree fruit expands with apple genome sequencing</title><description>An international team of scientists from Italy, France, New Zealand,  Belgium and the USA have published a draft sequence of the domestic  apple genome in the current issue of &lt;em&gt;Nature Genetics&lt;/em&gt;.
The availability of a genome sequence for apple will allow scientists  to more rapidly identify which genes provide desirable characteristics  to the fruit and which genes and gene variants provide disease or  drought resistance to the plant. This information can be used to rapidly  improve the plants through more informed selective breeding.
An organism's genome is the total of all its genetic information,  including genes. Genes carry information that determines, among other  things, a plant's appearance, health, productivity and color and taste  of the fruit.
The domestic apple is the main fruit crop of the world's temperate  regions. Apple is a member of the plant family Rosaceae which includes  many other economically important species, including cherry, pear,  peach, apricot, strawberry, and rose, to name just a few.
The state of Washington accounts for approximately 60 percent of  total apple production in the U.S. and Rosaceae fruit production is a  multi-billion dollar industry in the state. Washington state scientists  played an important role in the project.
Led by Washington State University horticultural genomicist Amit  Dhingra, the Washington-based team sequenced and analyzed a unique  version of the genome of the golden delicious apple in which all  duplicated chromosomes are genetically identical. This information was  used to validate the sequence of the more complicated "heterozygous"  golden delicious apple (in which duplicated chromosomes are not  identical).
"Before genome sequencing, the best we could do was correlate traits  with genes. Now we can point to a specific gene and say, 'This is the  one; this gene is responsible for this trait'. That trait of interest  might be, for instance, a disease, which is why sequencing the human  genome was such an important milestone. Or the trait might be for  something desirable, like flavor in a piece of fruit. We are already  working on finding physiological solutions to issues like bitter pit in  current apple varieties with the gene-based information available to us  and lay a foundation for improved varieties in the future through  generation of sports (mutations) and breeding," Dhingra said.
The Washington state contribution to the sequencing work was a  unique collaboration between the cross-state Apple Cup rivals of WSU and  the University of Washington.
Microbiologist Roger Bumgarner's lab at the University of Washington  provided the initial sequencing expertise and capability to the project,  which was later complemented and replaced by sequencing expertise in  the Dhingra genomics lab, who obtained the same DNA sequencing  instrument used in Dr. Bumgarner's lab.
"UW is a world leader in medical research and WSU is a world leader  in agricultural research," said Bumgarner. "Technological advancements  and techniques initially used to study medically important genomes and  problems can be rapidly applied to genomes and problems of agricultural  importance. We both had something to contribute and to learn from one  another. I think there are many more opportunities for such  collaborations to develop in the coming years."
After the sequencing was completed, WSU computational biologist  Ananth Kalyanaraman contributed to the analysis by comparing the apple  genome with that of pear, peach and grape to identify the differences  and commonalities that exist between these fruit crops.
While the apple genome provides a valuable resource for future  research, one pressing question answered by the international team's  paper in &lt;em&gt;Nature Genetics&lt;/em&gt; was one of origin. Scientists have long  wanted to know &amp;mdash; and have for years argued vehemently about &amp;mdash; the  ancestor of the modern domesticated apple. The question is now settled:  Malus sieversii, native to the mountains of southern Kazakhstan, is the  apple's wild ancestor. Now that that question is settled, scientists  will begin using the apple genome to help breed apples with desirable  new traits, including disease resistance and, potentially, increased  health-benefitting qualities.
"Having the apple genome sequence will greatly accelerate our ability  to define the differences between apple cultivars at the genetic  level," said Kate Evans, an apple breeder based at the WSU Tree Fruit  Research and Extension Center. "This will allow us to exploit these  differences and target areas of diversity to incorporate into the  breeding program, resulting in improved cultivars for the consumers that  are also better suited for long-term, sustainable production."
Dan Bernardo, dean of the WSU College of Agricultural, Human, and  Natural Resource Sciences, said, "The Washington apple is an icon of  quality around the globe. This is a natural home for the advanced  science necessary to map the tree fruit genome and actively study how it  functions."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5443</link><pubDate>Mon, 30 Aug 2010 03:24:19 PDT</pubDate></item><item><title>Researchers discover novel mechanism protecting plants against freezing</title><description>New ground broken by Michigan State University biochemists helps  explain how plants protect themselves from freezing temperatures and  could lead to discoveries related to plant tolerance for drought and  other extreme conditions.
"This brings together two classic problems in plant biology," said  Christoph Benning, MSU professor of biochemistry and molecular biology.  "One is that plants protect themselves against freezing and that  scientists long thought it had something to do with cell membranes, but  didn't know exactly how.
"The other is the search for the gene for an enigmatic enzyme of  plant lipid metabolism in the chloroplasts," in other words, how lipids,  which are membrane building blocks, are made for the plant cell  organelles responsible for converting solar energy into chemical energy  by photosynthesis.
In an article published online this week by the journal &lt;em&gt;Science&lt;/em&gt;,  Benning and his then-doctoral degree candidate Eric Moellering and  technical assistant Bagyalakshmi Muthan describe how a particular gene  leads to the formation of a lipid that protects chloroplast and plant  cell membranes from freeze damage by a novel mechanism in &lt;em&gt;Arabidopsis thaliana&lt;/em&gt;, common mustard weed. Working on his dissertation project under Benning, Moellering identified a mutant strain of &lt;em&gt;Arabidopsis&lt;/em&gt; that can't manufacture the lipid and linked this biochemical defect to  work done by others who originally described the role of the gene in  freeze tolerance, but did not find the mechanism.
"One of the big problems in freezing tolerance or general stress in  plants is that some species are better at surviving stress than others,"  Moellering said. "We are only beginning to understand the mechanisms  that allow some plants to survive while others are sensitive."
There is no single mechanism involved in plant freezing tolerance,  Moellering added, so he can't say that his findings will lead any time  soon to genetic breakthroughs making citrus or other freezing-intolerant  plants able to thrive in northern climates. But it does add to our  understanding of how plants survive temperature extremes.
Much plant damage in freezing temperatures is due to cell  dehydration, in which water is drawn out as it crystallizes and the  organelle or cell membrane shrivels as liquid volume drops. Lipids in  the membranes of tolerant plants are removed and converted to oil that  accumulates in droplets, the researchers said, retaining membrane  integrity, keeping membranes from fusing with one another and conserving  the energy by storing oil droplets. With rising concern globally about  water supplies and climate change, scientists see additional reasons to  understand the ways hardy plants survive.
The research, funded by the U.S. Department of Energy Office of  Science Basic Energy Sciences and the Michigan Agricultural Experiment  Station, also leads to speculation that freezing itself can prompt cell  proteins directly to change the composition of the membrane, without  activation by gradual acclimation. That has been a major focus in the  plant freezing tolerance field, the researchers said.
"This opens a huge door now for people to do this kind of research,  and to redirect researchers," Benning said. "There are lots of them out  there trying to understand cold, salt and drought tolerance in plants,  and we've given them a new idea about how they can approach this problem  mechanistically."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5424</link><pubDate>Fri, 27 Aug 2010 03:21:09 PDT</pubDate></item><item><title>UK researchers release draft sequence coverage of wheat genome</title><description>A team of UK researchers, funded by the Biotechnology and Biological  Sciences Research Council (BBSRC), has publicly released the first  sequence coverage of the wheat genome. The release is a step towards a  fully annotated genome and makes a significant contribution to efforts  to support global food security and to increase the competitiveness of  UK farming.
The genome sequences released comprise five read-throughs of a  reference variety of wheat and give scientists and breeders access to  95% of all wheat genes. This is among the largest genome projects  undertaken, and the rapid public release of the data is expected to  accelerate significantly the use of the information by wheat breeding  companies.
The team involved Prof Neil Hall and Dr Anthony Hall at the  University of Liverpool, Prof Keith Edwards and Dr Gary Barker at the  University of Bristol and Prof Mike Bevan at the John Innes Centre, a  BBSRC-funded Institute.
Prof Edwards said: "The wheat genome is five times larger than the  human genome and presents a huge challenge for scientists. The genome  sequences are an important tool for researchers and for plant breeders  and by making the data publicly available we are ensuring this publicly  funded research has the widest possible impact."
Universities and Science Minister David Willetts said: "This is an  outstanding world class contribution by the UK to the global effort to  completely map the wheat genome. By using gene sequencing technology  developed in the UK we now have the capability to improve the crops of  the future by simply accelerating the natural breeding process to select  varieties that can thrive in challenging conditions."
The genome data released are in a 'raw' format, comprising sequence  reads of the wheat genome in the form of letters representing the  genetic 'code'. A complete copy of the genome requires further  read-throughs, significant work on annotation and the assembly of the  data into chromosomes. Large-scale, rapid sequencing programmes such as  this have been made technically feasible by advanced technology genome  sequencing platforms, including one based on BBSRC-funded research  conducted in the UK in the 1990s.The majority of the sequencing work for  this particular project was done using the 454 Life Science platform,  developed in the US.
Prof Hall said: "The genome sequence data of this reference variety,  Chinese Spring wheat, will now allow us to probe differences between  varieties with different characteristics. By understanding the genetic  differences between varieties with different traits we can start to  develop new types of wheat better able to cope with drought, salinity or  able to deliver higher yields. This will help to protect our food  security while giving UK plant breeders and farmers a competitive  advantage."
The sequence data can be used by scientists and plant breeders to  develop new varieties through accelerated conventional breeding or other  technologies.
Prof Bevan, a member of the Coordinating Committee of the  International Wheat Genome Sequencing Consortium, said: "The sequence  coverage will provide an important foundation for international efforts  aimed at generating a complete genome sequence of wheat in the next few  years."
Prof Doug Kell, BBSRC Chief Executive, said: "Recent short-term  price spikes in the wheat markets have shown how vulnerable our food  system is to shocks and potential shortages. The best way to support our  food security is by using modern research strategies to understand how  we can deliver sustainable increases in crop yields, especially in the  face of climate change. Genome sequencing of this type is an absolutely  crucial strategy, building on previous BBSRC-funded work. Knowledge of  these genome sequences will now allow plant breeders to identify the  best genetic sequences to use as markers in accelerated breeding  programmes."
Dr Jane Rogers, Member of the Coordinating Committee of the  International Wheat Genome Sequencing Consortium and Director of BBSRC's  The Genome Analysis Centre, said: "The public release of the wheat  genome data will be a useful resource for scientists and the plant  breeding community and will provide a foundation to identify genetic  differences between wheat varieties. In recent years genomics technology  has advanced to a point that scientists can now produce sequence data  for plants with genomes as large as wheat at a rate unimaginable a few  years ago. This is an impressive achievement, notwithstanding the  significant hurdles we still face to fully interpret and understand the  data."
A key feature of this research has been the quick release of the  data into the public domain to allow other scientists and wheat breeding  companies to rapidly employ it in practical applications. Richard  Summers, Vice Chairman of the British Society of Plant Breeders, said:  "The wheat breeding community has been greatly impressed with the  collaborative approach taken in this project. The team brought together  world class skills in sequencing and wheat genetics to deal with a major  barrier in wheat breeding. This is an excellent example of how to  achieve technology transfer from research lab through to practical  deployment."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5421</link><pubDate>Fri, 27 Aug 2010 03:16:47 PDT</pubDate></item><item><title>Electrifying findings: New ways of boosting healthful antioxidant levels in potatoes</title><description>Here's a scientific discovery fit to give Mr. Potato Head static  cling and flyaway hair (if that vintage plastic toy had hair).  Scientists today reported discovery of two simple, inexpensive ways of  boosting the amounts of healthful antioxidant substances in potatoes.   One involves giving spuds an electric shock. The other involves zapping  them with ultrasound, high frequency sound waves.
Those new insights into improving the nutritional content of one of  the Western world's favorite side dishes were reported today at the  240th National Meeting of the American Chemical Society (ACS), being  held here this week. The study was among nearly 8,000 scientific reports  scheduled for presentation at the meeting, one of the largest  scientific gatherings of 2010.
"We found that treating the potatoes with ultrasound or electricity  for 5-30 minutes increased the amounts of antioxidants &amp;ndash;&amp;ndash; including  phenols and chlorogenic acid &amp;ndash;&amp;ndash; by as much as 50 percent," said Kazunori  Hironaka, Ph.D., who headed the research. "Antioxidants found in fruits  and vegetables are considered to be of nutritional importance in the  prevention of chronic diseases, such as cardiovascular disease, various  cancers, diabetes, and neurological diseases."
Hironaka, who is with Obihiro University in Hokkaido, Japan,  indicated that the process could have widespread commercial application,  due to growing consumer interest in so-called  "functional foods."   Those are products like berries, nuts, chocolate, soy, and wine that may  have health benefits beyond traditional nutrition. Such foods may  promote overall good health, for instance, or reduce the risk of  specific diseases. Hironaka estimated that sales of such products in the  United States alone now approach $20 billion annually.
"We knew from research done in the past that drought, bruising, and  other stresses could stimulate the accumulation of beneficial phenolic  compounds in fresh produce," Hironaka explained.  "We found that there  hasn't been any research on the healthful effects of using mechanical  processes to stress vegetables. So we decided in this study to evaluate  effect of ultrasound and electric treatments on polyphenols and other  antioxidants in potatoes."
The ultrasound treatment consisted of immersing whole potatoes in  water and subjecting them to ultrasound for 5 or 10 minutes. For the  electrical treatment, the scientists immersed potatoes in a salt  solution for 10 seconds and subsequently treated the spuds with a small  electrical charge for 10, 20, and 30 minutes. The study team then  measured antioxidant activity and the phenolic content and concluded  that the stresses increased the amount of these compounds.  The 5  minutes of ultrasound, for instance, increased polyphenol levels by 1.2  times and other antioxidants by about 1.6 times.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5377</link><pubDate>Mon, 23 Aug 2010 03:11:10 PDT</pubDate></item><item><title>New genetic tool helps improve rice</title><description>U.S. Department of Agriculture (USDA) scientists have developed a new tool for improving the  expression of desirable genes in rice in parts of the plant where the  results will do the most good.
Roger Thilmony, a geneticist with USDA's Agricultural Research Service (ARS), has shown that the &lt;em&gt;LP2&lt;/em&gt; gene promoter can be used to direct other introduced genes to express  beneficial traits in specific plant tissues without the potential for  causing unintended consequences. Thilmony works at the ARS Crop Improvement and Utilization Research Unit in Albany, Calif. ARS is USDA's principal intramural scientific research agency.
Rice is under constant threat from pathogens such as rice blast, a  fungus found in fields worldwide, and sheath blight, a continuing threat  to U.S. growers. Scientists who develop disease-resistant varieties  often find that introducing a gene may prevent disease in one part of  the plant, but also may reduce seed quality or produce other "side  effects" because the gene is expressed throughout the plant.  Tissue-specific promoters, such as &lt;em&gt;LP2&lt;/em&gt;, are segments of genes  that can direct the activity of introduced genes only to parts of the  plant where the beneficial traits are needed.
Thilmony and his ARS colleagues Mara Guttman, James Thomson and Ann Blechl found that the gene they named &lt;em&gt;LP2&lt;/em&gt; is consistently expressed in green tissues. In experiments, they fused the &lt;em&gt;LP2&lt;/em&gt; promoter with a "reporter gene" known to produce a specific enzyme, and  inserted that fused DNA package into seven lines of rice to see where  the enzyme would be produced.
They found that the &lt;em&gt;LP2&lt;/em&gt; promoter steered expression of the  reporter gene specifically to green tissues where photosynthesis occurs.  The reporter gene enzyme activity was highest in the leaves, and nearly  undetectable in the roots, seeds and flower parts.
The &lt;em&gt;LP2&lt;/em&gt; promoter could be used to improve varieties of rice,  barley and wheat and could aid in the development of biofuel crops, in  which scientists need to control leaf traits without affecting other  tissues, according to Thilmony.
The researchers published their work in &lt;em&gt;Plant Biotechnology Journal&lt;/em&gt; and have filed a provisional patent on use of the &lt;em&gt;LP2&lt;/em&gt; promoter.
This research supports the USDA priority of promoting international food security.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5358</link><pubDate>Fri, 20 Aug 2010 03:25:45 PDT</pubDate></item><item><title>Insects sense danger on mammals' breath</title><description>When plant-eating mammals such as goats chomp on a sprig of alfalfa,  they could easily gobble up some extra protein in the form of insects  that happen to get in their way. But a new report in the August 10th  issue of &lt;em&gt;Current Biology&lt;/em&gt;, a Cell Press publication, shows that  plant-dwelling pea aphids have a strategy designed to help them avoid  that dismal fate: The insects sense mammalian breath and simply drop to  the ground.
"Tiny insects like aphids are not helpless when facing large animals  that rapidly consume the plants they live on," said Moshe Inbar of the  University of Haifa in Israel. "They reliably detect the danger and  escape on time."
Inbar said he had always wondered about accidental predation of  small plant-dwellers based on his observations of insects that don't  really move around. "As soon as we started to work on this problem, we  suspected that the aphids responded to our own breath," he said. (The  researchers later used snorkels to keep their own breath from mucking up  their experiments).
The researchers allowed a goat to feed on potted alfalfa plants  infested with aphids. "Strikingly, 65 percent of the aphids in the  colonies dropped to the ground right before they would have been eaten  along with the plant," the researchers write.
That mass dropping might have been triggered by many cues: plant  shaking, sudden shadowing, or the plant-eater's breath. While a quarter  of the aphids dropped when plants were shaken, more than half fell to  the ground in response to a lamb's breath, the researchers report.
Shadows had no effect on the aphids' dropping behavior. Ladybugs, an  insect enemy of aphids, didn't inspire that kind of synchronous  response either.
Further studies with an artificial breath apparatus allowed the  researchers to test what it was about the breath that tipped the aphids  off. It turned out it wasn't carbon dioxide or other known chemical  ingredients found on mammalian breath. Only when the controlled  airstream was both warm and humid did it lead to impressive dropping  rates of 87 percent in a room with otherwise low humidity.
Inbar said that the aphids' "elegant solution" to the problem of  incidental predation is likely practiced by other species as well.
"This remarkable response to mammalian-specific cues, in spite of  the inherent cost of an aphid's dropping off the plant, points to the  significance of mammalian herbivory to plant-dwelling insects," the  researchers concluded. "We predict that this sort of escape behavior in  response to mammalian breath may be found among other invertebrates that  live on plants and face the same threat."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=5264</link><pubDate>Tue, 10 Aug 2010 03:42:53 PDT</pubDate></item></channel></rss>