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Plant polymerases IV and V are special forms of Polymerase II
January 07, 2009
It's a little like finding out that Superman is actually Clark Kent. A team of biologists at Washington University in St. Louis has discovered that two vital cellular components, nuclear RNA Polymerases IV and V (Pol IV and V), found only in plants, are actually specialized forms of RNA Polymerase II, an essential enzyme of all eukaryotic organisms, including humans. "We've caught evolution in the act," said Craig Pikaard, Ph.D., WUSTL professor of biology in Arts & Sciences. "We've known for decades that RNA Polymerases I, II and III are found in all eukaryotes, but it's only over the past several years that we've been aware that plants have two more nuclear polymerases, Pol IV and Pol V. Now it is clear that these enzymes evolved from Pol II over the past several hundred-million years. This is a new snapshot into the evolution of RNA polymerases, which are the enzymes responsible for decoding the information stored in the chromosomes." Analyzing purified Pol IV and Pol V by a sophisticated technique known as tandem mass spectrometry, the Pikaard lab and a team of collaborators at Pacific Northwest National Laboratory, led by Ljiljana Paa-Toli, discovered 12 subunits in both Pol IV and Pol V that correspond one-for-one to the 12 subunits of Pol II. Some of the Pol IV and Pol V subunits are encoded by the same genes as the corresponding Pol II subunits, but others come from duplicated Pol II subunit genes that have changed over time. Overall, four subunits of Pol IV are distinct from their Pol II counterparts, six subunits of Pol IV are different from their Pol II counterparts, and four subunits differ between Pol IV and Pol V. Yet, all of the Pol IV and Pol V subunits are "apples that haven't fallen far from the Pol II tree." The finding is important because it reveals more about the roles played by RNA in complex organisms. RNA polymerases are the enzymes responsible for making RNA from DNA templates. They are key players in determining which genes get switched on and which get turned off. RNA Polymerase II, for instance, is vital in the production of messenger RNAs that specify the amino acid sequences of each of the proteins in the cell. Despite having evolved from Pol II, Pol IV and V do not appear to be involved in protein synthesis, or to be absolutely essential for life. Instead, they have taken on specialized roles in gene silencing in plants. This is important to prevent the expression of potentially harmful genes, such as virus-derived "jumping genes" known as retrotransposons, and invading nucleic acids, such as the genomes of replicating viruses. The Pikaard lab has shown that Pol IV is required for the production of small interfering RNAs (abbreviated as siRNAs) that specify the silencing of matching DNA sequences, whereas Pol V makes longer RNAs that are thought to pair with the siRNAs at the affected chromosomal sites. Pikaard and his colleagues' work may have implications for applied medical research. For instance, gene therapy procedures sometimes use retroviral vectors as a way of introducing a foreign gene to replace a function impaired by disease. Often this foreign gene, called a transgene, restores the missing function for a while and then unexpectedly goes silent. The silencing process may have parallels to the pathway in plants that makes use of Pol IV and Pol V. Pikaard hypothesizes that Pol II accomplishes the functions of Pol IV and Pol V in other non-plant eukaryotes. The research revealing the subunit compositions of RNA Polymerases II, IV and V in the plant genus Arabidopsis was published online Dec. 23, 2008 in Molecular Cell. The work was supported by the National Institutes of Health and the U.S. Department of Energy. Pikaard's laboratory has been investigating the functions of Pol IV and Pol V since playing a leading role in their discovery in 2005. The Dec. 23 Molecular Cell paper is one of three related papers published by the Pikaard lab in rapid succession. In a paper published Nov. 14, 2008 in Cell, Pikaard and his colleagues explain how Pol IV and Pol V work together to use the non-coding region of DNA to prevent destructive, virus-derived genes from being activated. Then in a paper published Dec. 4 in Molecular Cell, the Pikaard lab announced a breakthrough in understanding the phenomenon of nucleolar dominance, the silencing of an entire parental set of ribosomal RNA genes in a hybrid plant or animal. That study is one of the first to demonstrate how siRNAs can play a role in controlling the dosage of vital genes, and not just harmful genes, and implicates the pathway in which Pol IV and Pol V function. The research of the Nov. 14 and Dec. 4 papers has been supported by the National Institutes of Health and by the National Science Foundation. Washington University in St. Louis

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The Polymerase Chain Reaction
by Kary B. Mullis (Editor), Francois Ferre (Editor), Richard A. Gibbs (Editor), J.D. Watson (Editor)
Edited by the inventor of polymerase chain reaction (PCR) and the 1993 Nobel Prize winner in Chemistry, Kary Mullis, as well as two experts in the field, this handbook provides up-to-date methodological protocols from the world's leading laboratories, in addition to new techniques and enhanced applications not yet available in book form. Nearly 40 chapters inform the novice and experienced PCR user on how to optimize their results. In the chapters on applications, researchers provide not only protocols, but also descriptions of how PCR has revolutionized their particular field. Future enhancements of PCR, as well as new potential uses, are discussed. Readers can learn how PCR has changed the face of diagnostic testing, cancer research, genetics, forensics, plant biology, DNA sequencing...
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Fever often absent in early enteroviral illness. (First Survey in Using PCR).(reverse-transcriptase polymerase chain reaction): An article from: Family Practice News
by Miriam E. Tucker (Author)
This digital document is an article from Family Practice News, published by International Medical News Group on January 15, 2003. The length of the article is 724 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: Fever often absent in early enteroviral illness. (First Survey in Using PCR).(reverse-transcriptase polymerase chain reaction) Author: Miriam E. Tucker Publication: Family Practice News (Magazine/Journal) Date: January 15, 2003 Publisher: International Medical News Group Volume: 33 Issue: 2 Page: 50(1)
Distributed by Thomson...
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![Selection of aptamers by systematic evolution of ligands by exponential enrichment: Addressing the polymerase chain reaction issue [An article from: Analytica Chimica Acta]](http://ecx.images-amazon.com/images/I/415FBN4EPVL._SX120__PC__PE00_.jpg)
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Selection of aptamers by systematic evolution of ligands by exponential enrichment: Addressing the polymerase chain reaction issue [An article from: Analytica Chimica Acta]
by M.U. Musheev (Author), S.N. Krylov (Author)
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description: Aptamers are DNA oligonucleotides capable of binding different classes of targets with high affinity and selectivity. They are particularly attractive as affinity probes in multiplexed quantitative analysis of proteins. Aptamers are typically selected from large libraries of random DNA sequences in a general approach termed systematic evolution of ligands by exponential enrichment (SELEX). SELEX involves repetitive rounds of two processes: (i) partitioning of aptamers from non-aptamers by an affinity method and...
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DNA Polymerases: Discovery, Characterization and Functions in Cellular DNA Transactions
by Ulrich Hubscher (Author), Silvio Spadari (Author), Giuseppe Villani (Author), Giovanni Maga (Author)
Maintenance of the information embedded in the genomic DNA sequence is essential for life. DNA polymerases play pivotal roles in the complex processes that maintain genetic integrity. Besides their tasks in vivo, DNA polymerases are the workhorses in numerous biotechnology applications such as the polymerase chain reaction (PCR), cDNA cloning, genome sequencing, nucleic acids-based diagnostics and in techniques to analyze ancient and otherwise damaged DNA. Moreover, some diseases are related to DNA polymerase defects, and chemotherapy through inhibition of DNA polymerases is used to fight HIV, Herpes and Hepatitis B and C infections. We have recently witnessed the discovery of an abundance of novel DNA polymerases in viruses, bacteria, archaea and eukaryotes with specialized properties...
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Poly(ADP-ribose) Polymerase: Methods and Protocols (Methods in Molecular Biology)
by Alexei V Tulin (Editor)
Poly (ADP-ribose) Polymerases (PARPs) are abundant and ubiquitous proteins that regulate crucial processes of the cell cycle, DNA repair, genomic stability, and transcriptional regulation. Being involved in basic cell functions, PARPs mediate rapid responses to such environmental factors as stress, infection, nutrition and hormonal signals. Whereas PARP inhibitors can suppress tumor growth and proliferation in certain breast, ovarian, and prostate cancers, understanding how PARP controls cellular functions is essential for the development of novel cancer treatments strategies. Divided into three convenient sections, Poly(ADP-Ribose) Polymerase: Methods and Protocols aims to explain how PARP proteins act within the normal development of an organism as well as in pathogenic conditions,...
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RNA Polymerase and Associated Factors, Part C, Volume 370 (Methods in Enzymology)
by Sankar Adhya (Editor), Susan Garges (Editor)
RNA polymerase is molecule important to gene transcription. Along with associated factors, RNA polymerase is part of the process in which RNA is transcribed to produce a protein.
* Construction and purification of RNA polymerases * DNA microarrays and bacterial gene expression * Functional analysis of transcription factors
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Methods in Enzymology, Volume 371: RNA Polymerase and Associated Factors, Part D
by Sankar Adhya (Editor), Susan Garges (Editor)
RNA polymerase is molecule important to gene transcription. Along with associated factors, RNA polymerase is part of the process in which RNA is transcribed to produce a protein.
* Models and methods for studying polymerase translocation * Assay for movements of RNA polymerase along DNA * Engineering of elongation complexes of bacterial and yeast RNA polymerases
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The 2009-2014 World Outlook for Polymerase Chain Reaction (PCR) Technologies
by Icon Group International (Author)
This econometric study covers the world outlook for polymerase chain reaction (PCR) technologies across more than 200 countries. For each year reported, estimates are given for the latent demand, or potential industry earnings (P.I.E.), for the country in question (in millions of U.S. dollars), the percent share the country is of the region and of the globe. These comparative benchmarks allow the reader to quickly gauge a country vis-a-vis others. Using econometric models which project fundamental economic dynamics within each country and across countries, latent demand estimates are created. This report does not discuss the specific players in the market serving the latent demand, nor specific details at the product level. The study also does not consider short-term cyclicalities that...
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Polymerase Chain Reaction (Pcr the Technique and Its Applications)
by Rosalind Eeles (Author), Alasdair C., Ph.D. Stamps (Author)
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Transcription of Ribosomal RNA Genes by Eukaryotic RNA Polymerase I (Biotechnology Intelligence Unit)
by Marvin R. Paule (Editor)
The mechanism by which ribosomal RNA is synthesized has been a topic of intensive research for nearly 30 years. In 1981 the first in vitro transcription system for ribosomal RNA from a eukaryote - mouse ascites cells - was reported, followed rapidly by similar systems in a variety of other eukaryotes, all revealed by a relatively small number of research groups. This monograph is the first to bring together the results and opinions of all these groups. Though it unavoidably emphasizes the common features of ribosomal RNA transcription between species, the species specificity of the process and nucleolar dominance and its possible mechanism(s) are also discussed.
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