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Non-member Achievement
Professor Philip Nelson Wins 2007 World Food Prize
Austin Nov.5, '07 . More often than not, those guiding  multifaceted plant breeding programs tend to forget, that side by side with the production of high yielding nutritious varieties, they need to ensure proper storage of food grains, vegetables, fruits and other perishable food products in order to minimize post-harvest loss due to diseases and insect attacks, unfavorable temperature changes as well as quality degradation in color, flavor and freshness during transportation.  Purdue University's Professor Dr. Philip Nelson, the current year's World Food Prize Winner dedicated his whole life in developing methods and  suitable equipment for application of those methods for safe storage of  all kinds of food both  in enormous quantities for shipment cross countries as well  as in small quantities from local distribution centers to individual consumers. The World Food Prize Committee have honored the outstanding scientist for  his visionary approach to solution of food problems in countries where food shortage is a chronic problem  for mitigating hunger and meeting nutritional requirements of the population. More >> 
Biotic and abiotic stress responses in plants meeting.
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A Cluster of Three Genes conferring submergence Tolerance to Rice
Austin, Aug. 10, ’06. In today’s (10 August 2006)  Nature 442, 705-708,  Kenong Xu and nine other rice geneticists affiliated to UCD, UCR and IRRI  have published a ground breaking paper entitled, “Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice.” They  have identified a cluster of three genes at the Sub1 locus, encoding putative ethylene response factors. Earlier authors have shown that a major QTL, Sub1 on chromosome 9 of. indica  rice cultivar FR13A,  confers flood tolerance up to two weeks of complete submergence. The above authors have shown that two of the three genes, Sub1B and Sub1C always characterize the Sub1 region of all rice accessions known for flood tolerance. These authors confirmed that  Sub1A-1  is a primary determinant  to complete submergence by over-expressing this gene in a flood-intolerant O. sativa ssp. japonica concomitant with  down regulating  Sub1C and upregulating  Alcohol dehydrogenase 1 (Adh1).  By incorporating the FR13A Sub1 gene into a widely grown Asian rice cultivar, these authors were able to produce a  flood tolerant variety,  combining the high yield and other agronomic traits of the recurrent parent.  The authors believe that  planting of this new variety will ensure enhanced rice production by protecting this crop against flood damage. Bangladesh, visited by flash floods at least once if not twice a year, will benefit greatly from this work as it will give the rice breeders a valuable clue to design breeding programs for evolving submergence tolerant rice varieties. IRRI has already developed an Indian rice variety called ‘Swarna’ incorporating the flood tolerance sub-1 locus and has currently launched a project of introducing the submergence locus into  a Bangladeshi variety, BR11. You can view the full paper by clicking the title of the paper. 
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Unraveling  Mystery of how Malarial Parasites Elude the Immune System
Austin Aug 9, 06. An article of great interest to scientists in general and biotechnologists in particular has been published  on August 4 online in Science.  It contains exciting findings of Volker Heussler and coworkers at the Bernhard Nocht Institute for Tropical Medicine in Hamburg, Germany. Until now scientists were unable to solve the mystery as to how the malarial parasites get away with immune system during their passage from the liver to the blood stream.  With the help of intravital imaging,  Volker’s team was able to trace  the migration of the parasites from the liver in infected mice to their blood stream. Their study reveal that after infected mosquito bites, malarial parasites make their way to the liver and change into a new form, infect red blood cells and multiply there at a very fast rate.    In that process they destroy the liver cells where they migrate. Thereafter, the infected cells detach themselves from their neighbors. Infected cells are then squashed and  they exit through tiny gaps in the walls of blood vessels in the liver. The mechanism “ensures both the migration of parasites into the blood stream and their protection from host immunity.” The finding  would usher in a new field of research leading to development of ways of stopping the malarial parasites in their tracks.
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IRRI Scientists to Bioengineer Rice Plants from C3 to C4 for More Yield
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ustin  Aug.15, ’06. In the 28th July issue of Science (vol. 313, p. 423), Dennis Normile reports of a consortium meeting held recently in IRRI. He reports that  in a bid to feed ever growing population in Asia likely to rise by 50%,  rice researchers  considered how to achieve a goal to increase rice yield by 50%.  They came to the conclusion that this is achievable not by the existing breeding tools but  by changing the photosynthetic  machinery of C3 rice plants to that of maize or any another  C4 crop that are 50 % more efficient at utilizing sunlight for production of  more biomass, requiring less water and a reduced dosage of fertilizers. According to rice experts, if successfully bioengineered, the yield of  a C4 rice plant  would increase by 50%.  This is because C4 plants are capable of utilizing elevated level of carbon dioxide around RuBisCO by  the activity  of an additional enzyme called PEP carboxylase. In C4 plants photorespiration, characteristic of C3 plants is  also suppressed.  IRRI breeders, led by  John E. Sheehy, an expert in crop ecology and crop modeling,  hope to come up with such a photosynthetically more efficient variety by the year 2010. In addition to transfer C4  genes from maize, the IRRI breeders will screen their rich germplasm comprising 6000 wild rice  collection and hopefully may detect C4 pathway,  already in existence  in some of their material.
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Nutritional Enzyme in GM Wheat Withstand Boiling Temp without Damage
Austin  June 27, 2006. That cooked food lose their nutritional enzymes due to excessive heat during their preparation is a well known fact. For instance, at 63 degrees Celsius,  the enzyme phytase, which helps the human system to absorb zinc and iron is inactivated in wheat and barley. It has been estimated that due to destruction of these enzymes during cooking, 2-3 billion people worldwide, mostly in developing countries suffer from nutritional deficiency. The effect is more acute among children making them susceptible to pneumonia and watery diarrhea claiming a heavy toll of their lives. Henrik Brinch-Pedersen and co-workers at the Danish Institute of Agricultural Sciences have come up with a solution.  By inserting a phytase gene from the fungus Aspergillus fumigatus, they have bioengineered transgenic wheat and barley lines in which phytase remains stable up to 89 degrees of Celsius.  They have demonstrated that even after boiling for 20 minutes bioengineered (GM) wheat grains retain enough phytase activity enabling consumers to intake sufficient amounts of minerals. The above finding has been published in the 2nd June issue of the Journal of Agricultural and Food Chemistry.
Henrik Brinch-Pedersen, Frank Hatzack, Eva Stöger, Elsa Arcalis, Katrine Pontopidan, and Preben B. HolmHeat-Stable Phytases in Transgenic Wheat (Triticum aestivum L.): Deposition Pattern, Thermostability, and Phytate Hydrolysis. J. Agric. Food Chem.; 2006; 54(13) pp 4624 - 4632.
(Courtesy SciDev.net, 28th June, 2006)

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ENGINEERING LIFE: Building a FAB for Biology
Austin 29th of May, ’06. An article entitled, Engineering life: Building a FAB for Biology has been published in the June issue of Scientific American (Vol. 294 Issue 6, p44-51).  Nine top class scientists headed by Baker David, representing different facets of biotechnology advocate that time is rife, when current  computational knowledge should be combined with that of latest DNA manufacture technology.  The article begins by an introductory remark that the best available machines for DNA synthesis  have the capacity of adding a nitrogenous base: adenine, cytosine, guanine and thymine  every five minutes. Compared to man made machinery, its biological counterpart such as DNA polymerase  adds 500 bases a second with an error of only one base in a billion. Since a number of polymerases  work simultaneously in a living organism of which one of the examples is  a bacterium, a long stretch of DNA  comprising about five million nitrogenous bases are synthesized in a matter of 20 minutes.  The fabrication of biological systems as applied to  bioengineering requires participation of the following: systems (human encoded functions of biological devices), devices (combination of parts each of which carries out a separate task), parts (pieces of DNA that work with a matching binding protein to regulate gene activity  and DNA (DNA parts specified by designers.). I may also mention here about a very useful site that will help the readers understand  this article. Read the whole summary by clicking here.
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Vaccine against cervical cancer will save millions of lives
Austin June 9, 2006. The world woke up today with an exceptionally good news – the news of the approval of a cancer vaccine by FDA. The vaccine will work against  four strains  of human papilloma virus that cause cervical cancer (cf. Hopkins virologist Keerti Shah) by immunizing  the majority of would-be victims. Instead of injections, the vaccine can be inhaled to prevent the attack of the cancer. Interestingly, women of developing countries will benefit most where, reports say, the incidence of attack every year is nearly 400,000.  The mortality among women of developed countries from this disease is considerably less because of the facility available to them for annual screening and treatment thereafter.   
 Researchers at Professor Richard Schlege’s lab of Georgetown University Medical Center Washington D.C.  took  nearly 20 years to develop the vaccine. The vaccine is composed of a protein molecule that makes up the outer shell of the virus. The protein molecule elicits an immune response which ultimately results in the destruction of the virus.
The name of the vaccine made by Merck is Gardasil. The company claims that it  is 100 per cent effective against vaginal and vulval cancers. That HPV causes  both these diseases has been established. The name of the second vaccine,  to be marketed by GlaxoSmithKline's, is called Cervarix. It has been shown to generate  an antibody response in women aged 26–55 years. It prevents the occurrence of the above diseases by almost 100 per cent.  By clicking the hyperlink, you may be able to view the image of this virus illustrated in the article provided by SciDevNet.
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ENGINEERING LIFE: Building a FAB for Biology
Austin 29th of May, ’06. An article entitled, Engineering life: Building a FAB for Biology has been published in the June issue of Scientific American (Vol. 294 Issue 6, p44-51).  Nine top class scientists headed by Baker David, representing different facets of biotechnology advocate that time is rife, when current  computational knowledge should be combined with that of latest DNA manufacture technology.  The article begins by an introductory remark that the best available machines for DNA synthesis  have the capacity of adding a nitrogenous base: adenine, cytosine, guanine and thymine  every five minutes. Compared to man made machinery, its biological counterpart such as DNA polymerase  adds 500 bases a second with an error of only one base in a billion. Since a number of polymerases  work simultaneously in a living organism of which one of the examples is  a bacterium, a long stretch of DNA  comprising about five million nitrogenous bases are synthesized in a matter of 20 minutes.  The fabrication of biological systems as applied to  bioengineering requires participation of the following: systems (human encoded functions of biological devices), devices (combination of parts each of which carries out a separate task), parts (pieces of DNA that work with a matching binding protein to regulate gene activity  and DNA (DNA parts specified by designers.) . I may also mention here about a very useful site that will help the readers understand  this article. Read the whole summary by clicking here.
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Immobile Protein Assemblies at the Plasma membrane of the yeast
Austin March 1, '06. In a feature article published  in Nature (439, 998-1003), Tobias C. Walther et al. at the Howard Hughes Medical Institute and Department of Biochemistry and Biophysics, University of California at San Francisco, report of large immobile protein assemblies at the plasma membrane in the yeast Saccharomyces cerevisiae. These assemblies  are called  eisosomes . They consist primarily of  two cytoplasmic proteins, Pil1 and Lsp1 and serve as  endocytic sites. A plasma membrane protein, Sur7, is associated with eisosomes. They are involved in endocytosis  - a process by which cells internalize molecules with a specific binding protein in the cell.
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Mechanism of selenoprotein Translation Bypassing Nonsense Mediated Decay Austin March 16, '06. In an article captioned, "Nuclear Assembly of UGA Decoding Complexes on Selenoprotein mRNAs: a Mechanism for Eluding Nonsense-Mediated Decay." published in Mol. Cell. Biol. vol. 26. 5:1795-1805 (2006), Lucia A. de Jesus at the Dept. Cell, Mol Biol., Univ. of Hawaii, Honolulu  and his colleagues at Harvard Medical School, have described a novel mechanism allowing seleno-protein  mRNAs  to get around non-sense mediated decay (NMD) and translating the mRNA into selenoprotein. Seleno-protein is a protein that contains the essential trace element selenium in the form of seleno-cysteine.  When insertion of selenocysteine into selenoproteins takes place, it becomes a stop codon, UGA leading to the decay of the protein, a process called nonsense-mediated decay (NMD). In other words, seleno-proteins are degraded by NMD. The authors detected co-localization  of two important proteins, namely, EFsec and SBP2 in cells where SBP2  was present in sufficient amounts.  Their findings further revealed that there is shuttling of SBP2 between the nucleus and the cytoplasm and that there is functional nuclear localization and export signals in the above two proteins. They also found evidence that EFsec localization is influenced by the levels of SBP2. Thus, they were able to explain the mechanism how the nuclear assembly of the selenocysteine incorporation machinery bypass nonsense-mediated decay allowing selenoprotein translation.
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Assembly of Mammalian Chromosomes at the Equator without Bipolar Attachment
Austin March 28, '06. Kapoor at the  Laboratory of Chemistry and Cell Biology, the Rockefeller University, New York and his associates at collaborative institutes, in a report published in a recent issue of Science (vol. 311: 388-91) have shown  that in  mammalian cell mitosis,  chromosomes may move to the equator before they become attached to the opposite poles of the bipolar spindle, a condition termed as "biorientation". This finding runs counter to the former notion that for the mitotic chromosomes to assemble at the equator, each one of them requires to be "bioriented." These authors employed a number of highly advanced techniques, namely, a) reversible chemical inhibitors, b) live-cell light microscopy, and c) correlative electron microscopy, to prove  that mono-oriented chromosomes; i.e., chromosomes attached to the spindle by one of the two kinetochores can move to the equatorial plate by gliding  along with other already bioriented chromosomes. The authors suggest that the end-directed microtubule motor CENP-E (kinesin-7) plays an important role in the movement of mono-oriented chromosomes to the equator.
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Control of  Deadly Rice Blast Fungus is possible within Foreseeable Future
Austin March 28, 06. In  a paper captioned, "A P-type ATPase required for rice blast disease and induction of host resistance" published in the 23rd March, '06  issue of  Nature  (40, 535-539), Martin J. Gilbert, Christopher R. Thornton, Gavin E. Wakley and Nicholas J. Talbot at the School of Biosciences, University of Exeter, have reported how the gene MgAPT2 in the rice blast pathogen Magnaporthe grisea paralyses the host defense mechanism causing annually an extensive rice crop loss, enough to feed 60 million people. The base sequence of this deadly fungus has been recently worked out and it is hoped that  by manipulating this gene, its virulence can be greatly minizmised. In the paper, the authors have shown that the mutant form of this gene is unable to infect the rice plant because it fails to secrete extra-cellular enzymes necessary for invading the host with its appressoria.
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An Exciting finding: FCA - An Abscisic Acid Receptor
Austin 22nd Jan. 06. In the 19th   January issue of Nature, (vol. 439, 290 - 294),  Robert D. Hill and his  associates at the Plant Science Department, University of Manitoba, Winnipeg, Canada reported that FCA, a nuclear RNA-binding protein involved in the transition to flowering, is an ABA receptor.  The above authors have shown in Arabidopsis that FCA and ABA interact, inhibiting the transformation of  shoot meristems from vegetative to flowering status.  FLC, a MADS box transcription factor, inhibits the transition to flowering. FCA interacts with a nuclear transcription factor, FY and, in so doing, prevents formation of FLC, allowing the transition to flowering. ABA, in binding to FCA, prevents its interaction with FY, thus, allowing continued synthesis of FLC and delay of the transition to flowering. Their data  have further  revealed that  the autoregulation of FCA is inhibited when full length FCA mRNA binds ABA.  Their study further suggests that ABAP1 protein isolated from barley that bound ABA in vitro has regions of similar amino acid sequence to that of FCA.

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Origins of DNA: Base invaders
Austin 13 Jan. 06 In this week's (12th January, 06) Nature, John Whitfield discloses some exciting information in an article entitled, "Origins of DNA: Base Invaders" under the section "News Feature".  In the beginning of life, there was no DNA and all the information was stored only in RNA. RNA is a  multipurpose molecule  which also plays the role of an enzyme.  According to Patrick Forterre, the French evolutionary biologist, in the course of evolution, viruses took over the world of RNA insidiously, and brought about the change by adopting DNA as an information vehicle. Such an invasion by viruses allowed them to bypass the defense mechanism put up by RNA-based cells.
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PTC124 a potential Drug in the cure for Cystic Fibrosis and other Congenital diseases. Austin Dec 15, '05.  In the December 8 issue of Nature (vol. 438:726-28),  Dr. C. Ainsworth discusses in a news article entitled "Nonsense mutations: Running the red light", the importance of  "Nonsense Mutations" in the cure for a genetic disease. She briefly describes how a protein is made from a gene:  DNA -> messenger RNA (mRNA)-> ferried across the nuclear membrane into the ribosomes which act as a molecular factory where amino acids are assembled into a specific protein according to the blueprint contained in the mRNA sequence. There are 64 codons of which 61 encode for 20 essential amino acids that constitute a functional protein and three  signify the end of the message. In patients suffering from congenital diseases such as cystic fibrosis, the message is stopped by  means of a mutation which converts an amino acid codon  into a 'stop' codon.  In other words, the genetic message terminates before the functional protein is synthesized.   The kind of symptoms exemplified by cystic fibrosis is called "nonsense mediated decay" (NMD in short). An under trial  drug called PTC124 halts this process. Instead of making faulty protein, it helps the ribosomal machinery to proceed making the specific protein by ignoring the stop codon. In patients suffering from a severe type of congenital anaemia called thalassaemia, a premature stop codon intervenes the specific mRNA.  Scientists  found explanations for rare cases where thalassaemia patients survived. In these exceptional individuals the premature stop codon appears too late instead of  in the middle of the mRNA message sparing their lives. In the treatment of  diseases such as cystic fibrosis, the PTC124 drug has entered Phase II efficacy trials on adult patients in both the United States and Israel.

Recreation of A Deadly Flu Virus – A Sensational  Achievement

First Report of Gibberellin Receptor  in A Rice Mutant

Gene interrupting Sugar Flow in Rice Pollen during Cold Spells
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Simultaneous Incorporation of  two Bt genes in indica basmati rice 
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Novel mRNA Changing from  Non-coding to Coding  Status upon Cellular Stress
Austin Nov 22, 2005. A new kind of novel messenger RNA has been reported by CSHL research scientists led by David Spector in the October 21, 2005  issue of Cell (123:249-63).  They have reported that viral infection or similar cellular stresses convert a normally non protein-coding RNA to a protein-coding mRNA. K. Prasanth, a postdoctoral at Spector's lab identified for the first time a mouse gene called mCAT2 that encodes a cell surface receptor protein. Further studies in that lab revealed that mCAT2 gene encodes two different kinds of RNAs: a typical mRNA that is ferried across the nuclear membrane and an atypical one that stays in the nucleus.  Results reported elsewhere gave this group a clue that the mCAT2 receptor activates nitric oxide production and that a number of stress conditions such as wound healing and viral infection stimulates the receptor synthesis.
In order to verify that synthesis of the receptor is stimulated by stress conditions Spector's group treated cells with interferon in order to artificially create stress conditions similar to the symptoms caused by viral infection. They observed that the interferon treatment activated mCAT2 gene expression. Later, the atypical non-protein-coding mCAT2 mRNA was cleaved post- transcriptionally to produce protein-coding mRNA that was subsequently ferried across the nuclear membrane to the cytoplasm and translated into protein like its typical counterpart. Spector views this discovery to be a new type of gene regulation  and predicts that in the  future  a large family of similar regulatory genes may come to light in humans and other organisms

A New Approach for Pest Control by Manipulating Pheromone Signaling: Dr. Pingxi Xu bags the 2005 International Prize in Neurobiology

Austin Nov. 07, '05. In a prize winning* article, “A Drosophila OBP Required for Pheromone Signaling” published in Science, Vol. 310: 798-799 , 4 November 2005, Pingxi Xu at the Department of Basic Neuroscience and Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX demonstrated that in addition to pheromone-responsive receptor, a protein belonging to OBP (Odorant Binding Protein) family plays an important role in olfactory neuron response induced by the pheromone, VA (cis-vaccenyl acetate). In a fruit fly, Drosophila VA is secreted to elicit aggregation behavior (to attract both sexes, male and female together). Using a recessive Drosophila mutant. lush, the author showed that the mutants, lose their VA sensitivity and fail to be attracted by VA revealing that the binding protein is required for pheromone perception. By expressing a wild-type lush transgene in the mutants, he was able to restore VA sensitivity, thereby providing further proof of the unequivocal role of OBP in pheromone signaling. The author concluded that it is an important finding in that the method can be applied to manipulate insect behavior to control pests that spread human diseases and cause agriculture losses in a species-specific manner.
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*The 2005 international Prize in Neurobiology by the journal Science and Eppendorf.

Genetic diversity of Indian rice varieties,  landraces and 3 spp.  of Oryza
Austin May 05, 05
. In a research article, “Use of anchored (AG)n and (GA)n primers to assess genetic diversity of Indian landraces, and varieties of rice published in  Current Science (Vol. 89, 1371-81, 2005), N. Sarla, C. N. Neeraja and E. A. Siddiq at the Directorate of Rice Research, Hyderabad, India report the results of their study on the phylogenetic relationships between land races, cultivars and three Oryza species including O. sativa.  Using fingerprinting and  GA repeats the authors came to the conclusion that heterozygosity between rice varieties was less marked than between the latter and landraces. A comparison between four wild accessions of two Oryza species, namely, O. nivara and O. rufipogon revealed that  they collectively were phylogenetically more related  to the varieties than to landraces. The authors recommend that adoption of adequate measures to conserve landraces is essential in order to broaden the  narrow genetic base of modern rice varieties. Their results further indicate that  for determination of genetic diversity,  (AG)n and (GA)n based primers are  both informative and cost effective.
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Rice Chromosomes 11 and 12 Rich in Disease Resistance Genes
Austin Oct. 10, '05. An article entitled, “The sequence of rice chromosomes 11 and 12 , rich in disease resistance genes and recent gene duplications” has just been published in BMC Biology 2005, 3:20 by the Rice Chromosomes 11 and 12 Consortia. The complete base sequences of rice chromosomes 11 and 12 have been determined and characterized. These two chromosomes form about one-seventh of the whole genome. The Consortia identified 6000 genes (5% of the total) which confer resistance to various diseases attacking rice. The number of disease resistant genes resident in the above two chromosomes are greater in proportion than those on the remaining 10 chromosomes. The rice sequencing material was Oryza sativa ss japonica cv. Nipponbare. Contact Dr. Joachim Messing: messing@waksman.rutgers.edu for further information.

Recent Updates in RNA - A Special Issue of  Science devoted to this Topic
In the “Introduction to Special Issue”  of Science, vol. 309, published on the 2nd of September,  Riddihough Guy  updates  the readers with the latest development that has taken place in the realm of RNA. In  an article, “Forests of RNA Dark Matter”, he gives an overview of 17  articles dealing with  different aspects of  RNA appearing in the same issue of Science.  In the article he chooses the theme of  these articles and explains what they are about.  Whatever information is attributed to the author, they are taken from different articles that have appeared in the above issue; only at two places the names of the authors have been given.
The author begins the article revealing that until recently, knowledge about RNA particularly of the noncoding type was limited. He draws a parallel between RNA and  protein in that an RNA group I self-splicing intron uses two metal ions for phosphoryl  transfer similar to that reported in many protein enzymes. He talks of an unusual loop like-mRNA at the 5’ end. That unusual piece of mRNA seems to protect the mRNA from degradation. Quoting Moore’s work, he mentions about the teams of proteins that participate in regulating mRNA activity in various developmental stages from their birth to death.  He discusses the role  of  cytoplasmic  P–bodies,  which serve as  temporary storage space  for  many mRNAs after they perish; about non-translating mRNAs that  are also housed  in these temporary  storehouse.  He also describes the contribution made by  Zamore and Haley who elucidated the role of two more RNA components: microRNAs (miRNAs) and  small interfering RNAs (siRNAs)  that take part in RNA silencing.  Recent reports have shown that not only can miRNAs  repress the initiation of translation  but also contribute to enhance mRNA production. Click
here to read the remainder  of the summary and the titles of different  articles (in September 2  issue of Science) based on which the summary has  been written.
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Recreation of A Deadly Flu Virus – A Sensational  Achievement
Austin Oct. 6, 2005. The 1918 Spanish flu virus, which may have killed nearly 50 million people in the USA, has been  recreated by a team of scientists led by Jeffery Taubenberger of the armed Forces Institute of Pathology in Rockville, Maryland. The paper which has just been published online in Nature on October 5, 2005  gives details of the hitherto unknown base sequences of the three genes of this deadly virus. This  completed  the entire genomic sequence of this virus. When the researchers infected mice with the reconstituted virus, it turned out to be extremely virulent. Compared to a modern flu strain, it produced 39,000 times more virus particles showing its degree of lethality.   The infected mice did not die when researchers replaced the haemagglutinin  gene which helps virus enter cells. The virulence was considerably  abated when three polymerase genes that help the virus replicate were substituted. Further research in this deadly virus will be of  great help to produce vaccine and design drug to contain this virus.
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First Report of Gibberellin Receptor  in A Rice Mutant

 
October 3, '05. In the Sep 29 issue of Nature (vol. 437:693-8), Ueguchi-Tanaka and associates at the Department of Bioscience and Biotechnology, Nagoya University, Japan have reported in rice a hitherto unknown receptor for gibberellin in the gibberellin insensitive dwarf1 mutant, gid1. They have further reported that its normal allele, GID1 encodes an unknown protein  matching  the hormone-sensitive lipases and that there is a preferential localization of a GID1-green fluorescent fusion protein (GFP) signal in nuclei. Furthermore, they have shown that over-_expression of GID1 produces a GA-hypersensitive phenotype.  Based on their data they concluded that GID1 functions to give rise to a soluble receptor regulating GA signaling in rice.

Incorporation of prokaryotic genes into New World Cotton resulting in better fiber quality
In Plant Cell Reports  (22:691–697, 2004), X. Li  and  associates at  the College of Agriculture and Biotechnology, China have reported that using Agrobacterium, they  have successfully transferred  genes, acsA and acsB from a cellulose producing bacterium, Acetobacter xylinum to brown cotton (Gossypium hirsutum L.)  pollen by means of vacuum infiltration.  Crosses of normal cotton plants with transformed pollen yielded eight transgenic plants out of over 1000 seeds.  Seeds were germinated and grown in a nutrient medium containing 50 mg/ml hygromycin.  The authors have further reported that the fibers of  transgenic cotton plants were stronger by 15% with a higher cellulose content than  the control. According to the authors  the future holds a great promise for improving the quality of cotton fibers by  expressing the bacterial acsA and acsB genes in standard cotton varieties.

[GNOBB congratulate the Chinese scientists for their extraordinary accomplishment. If the results reported by them, can be repeated elsewhere, it will revolutionize cotton industry through production of high quality stronger cotton fibers.]

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