
Science Resources RSS Feeds
|
 |
 |
 |
Molecular typesetting -- proofreading without a proofreader
June 23, 2009
Researchers at the Universities of Leeds and Bristol (UK) have developed a model of how errors are corrected whilst proteins are being built. Ensuring that proteins are built correctly is essential to the proper functioning of our bodies, but the 'quality assurance' mechanisms that take place during this manufacturing process are not fully understood.
"Scientists have been puzzled as to how this process makes so few mistakes", says Dr Netta Cohen, Reader at the University of Leeds' School of Computing.
To create a protein, the first step involves copying the relevant gene on our DNA onto a template, called RNA. This copying process is carried out by molecular machines called RNA polymerases.
"The RNA polymerase acts like an old fashioned newsprint typesetter, constructing newsprint by assembling letters one at a time. Similarly, RNA polymerase constructs RNA by reading the DNA and adding new letters to the RNA one at a time," explains Dr Cohen.
There's no way for the RNA polymerase to ensure that the correct letter is always incorporated at the right spot. "Statistically, we would expect to see a hundred-fold more errors than we actually do, so we know that some error correction must be happening. Otherwise, many more proteins in our bodies would malfunction," says Dr Cohen.
Biological experiments have shown that the RNA polymerase slides both forwards and backwards along the RNA sequence it has created. What's more, it has miniature scissors that can then cut out the last few letters of RNA.
So how are errors corrected? Intelligent typesetters would remove the last few letters when they spot an error. The new model suggests how the backward sliding stalls when passing an error, so wrong letters can be snipped off and copying can resume.
"The mechanism we've modelled has only recently been shown to be implicated in proofreading," says Dr Cohen. "In fact, there is more than one identified mechanism for ensuring that genetic code is copied correctly. The challenge now is to find out - through a combination of experimental biology and modelling - which mechanism is dominant."
University of Leeds
|
 |
Related Polymerase Current Events and Polymerase News Articles Polymerase Current Events and Polymerase News RSS GEN reports on enhancing the applications of qPCR Quantitative polymerase chain reaction (qPCR) technology is experiencing a surge of interest and rapid expansion as a result of advances such as instrumentation that pushes capacity to 1,536 wells and optimization-free multiplexing.
Wild pigs and deer do not spread GM corn via feces or accumulate transgenic residues in meat Deer stew, roast of wild boar, venison ragout - come fall, all varieties of game are in season for gourmets. However, ever since the worldwide surge in genetically modified corn, critical consumers' appetites have abated somewhat.
Catching a killer one spore at a time A workshop at the Smithsonian Tropical Research Institute in Panama has dramatically improved the ability of conservationists and regulatory agencies to monitor the spread of chytridiomycosis-one of the deadliest frog diseases on Earth.
Whale-sized genetic study largest ever for southern hemisphere humpbacks After 15 years of research in the waters of the South Atlantic and Indian Oceans, scientists from the Wildlife Conservation Society, the American Museum of Natural History, and an international coalition of organizations have unveiled the largest genetic study of humpback whale populations ever conducted in the Southern Hemisphere.
How RNA polymerase II gets the go-ahead for gene transcription All cells perform certain basic functions. Each must selectively transcribe parts of the DNA that makes up its genome into RNAs that specify the structure of proteins.
Frozen assets: NIAID researchers turn to unique resource for clues to norovirus evolution A search through decades-old frozen infant stool samples has yielded rich dividends for scientists from the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.
Gut Ecology in Transplant Patients Small-bowel transplant patients with an ileostomy -- an opening into their small bowel -- have a very different population of bacteria living in their gut than patients whose ileostomy has been closed, researchers from UC Davis and Georgetown University Medical Center have found.
NIST calculations may improve temperature measures for microfluidics If you wanted to know if your child had a fever or be certain that the roast in the oven was thoroughly cooked, you would, of course, use a thermometer that you trusted to give accurate readings at any temperature within its range.
Test developed at UQ diagnosed Australia's first swine flu victim When the first cases of H1N1 Influenza (swine flu) were reported in Mexico in April, UQ researchers got to work developing a test to diagnose the virus.
Bird flu leaves the nest -- adapting to a new host Current research suggests that viral polymerase may provide a new therapeutic target for host-adapted avian influenza. More Polymerase Current Events and Polymerase News Articles
|
 |

|
The Polymerase Chain Reaction
by Kary B. Mullis (Editor), Francois Ferre (Editor), Richard A. Gibbs (Editor), J.D. Watson (Editor)
This is the first comprehensive handbook on polymerase chain reaction (PCR). Edited by the inventor of PCR and the 1993 Nobel Prize winner in Chemistry, Kary Mullis, and two prominent experts in the field. It provides the most up-to-date methodological protocols from the world's leading laboratories, as well as exciting new techniques and enhanced applications not yet available in book form. Nearly forty chapters will inform the novice and experienced PCR user on how to optimize their results. The applications chapters are quite unique, with the foremost researchers providing not only protocols, but descriptions of how PCR has revolutionized their particular field. Future enhancements of PCR as well as new potential uses are discussed. Readers will learn how PCR has changed the...
|

|
"Flexi DNA Polymerase - GoTaq Polymerases and Master Mixes, Promega - Model PAM8298 - Each"
by Promega
Flexi DNA Polymerase - GoTaq Polymerases and Master Mixes, Promega - Model PAM8298 - Each : DNA polymerase is a Taq polymerase in a formulation that provides a robust performance in a variety of applications. It is supplied with two reaction buffers, one of which contains a green dye that separates. The colorless buffer is recommended for applic
|

|
RNA Polymerases as Molecular Motors (RSC Biomolecular Sciences)
by Henri Buc (Editor), Terence Strick (Editor)
This book, written by expert scientists in the field, analyses how these diverse fields of research interact on a specific example - RNA polymerase. The book concentrates on RNA polymerases because they play a central role among all the other machines operating in the cell and are the target of a wide range of regulatory mechanisms. They have also been the subject of spectacular advances in their structural understanding in recent years, as testified by the attribution of the Nobel prize in chemistry in 2006 to Roger Kornberg.
The book focuses on two aspects of the transcription cycle that have been more intensively studied thanks to this increased scientific cooperation - the recognition of the promoter by the enzyme, and the achievement of consecutive translocation steps...
|
|
|
The Polymerase Chain Reaction and the Analysis of the t Cell Receptor Repertoire (Medical Intelligence Unit)
by Jorge R. Oksenberg (Author), Panzara Michael A. (Author), Lawrence Steinman (Author), Michael A. Panzara (Author)
This text describes the molecular biology of the components of the trimolecular complex and focuses on current knowledge of major mechanisms that shape the TCR repertoire. It provides a detailed description of the method and general applications of PCR in research and clinical medicine and describes each system, providing recent examples along with the advantages and disadvantages of the techniques. Also included is the use of quantative PCR in TCR analysis. The book summarizes the recent extensive bibliography where PCR-based methods are being used to analyze TCR expression and repertoire in normal and pathological conditions such as cancer, transplantation, immunodeficiencies, superantigenic stimulation and autoimmune lesions, especially multiple sclerosis and rheumatoid arthritis.
|
|
|
Ribonucleic Acid Polymerase and the Regulation of Transcription: Symposium Proceedings
by William S. Reznikoff (Editor), etc. (Editor)
|
|
|
Polymerase Chain Reaction (Pcr the Technique and Its Applications)
by Rosalind Eeles (Author), Alasdair C., Ph.D. Stamps (Author)
|

|
Viral Polymerases and Related Proteins, Volume 275 (Methods in Enzymology)
by John N. Abelson (Editor), Melvin I. Simon (Editor), Lawrence C. Kuo (Editor), David B. Olsen (Editor), Steven S. Carroll (Editor)
The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. More than 270 volumes have been published (all of them still in print) and much of the material is relevant even today--truly an essential publication for researchers in all fields of life sciences.
Key Features * Expression, purification, and characterization * Activity assays * Kinetic and screening * Design and analysis of substrates and inhibitors * Molecular and structural characterizations
|

|
"Hot Start Polymerase - GoTaq Polymerases and Master Mixes, Promega - Model PAM5008 - Each"
by Promega
Hot Start Polymerase - GoTaq Polymerases and Master Mixes, Promega - Model PAM5008 - Each : DNA polymerase is a Taq polymerase in a formulation that provides a robust performance in a variety of applications. It is supplied with two reaction buffers, one of which contains a green dye that separates. The colorless buffer is recommended for applic
|

|
The Polymerase Chain Reaction (PCR) for Human Viral Diagnosis (Pcr for Human Viral Diagnosis)
by Jonathan P. Clewley (Author)
The polymerase chain reaction (PCR) is the most sensitive method for revealing the presence of otherwise undetectable quantities of the genome of RNA or DNA of human viruses. The Polymerase Chain Reaction (PCR) for Human Viral Diagnosis addresses the urgent need to use this revolutionary technology in reference and routine diagnostic laboratories. It informs the molecular biologist of the most appropriate clinical uses for PCR and educates the clinician and medical virologist about the subtleties and benefits of gene amplification. The reader is given an understanding and appreciation of the principles of PCR and how, why, and where it should be applied. The book explains the principles behind PCR and its role in the diagnostic and public health laboratory. The application of PCR to the...
|
|
|
Haplotypes without children: PCR applied to close loci on individual human sperm. (polymerase chain reaction): An article from: Human Biology
by B. Crouau-Roy (Author), J. Clayton (Author)
This digital document is an article from Human Biology, published by Wayne State University Press on February 1, 1995. The length of the article is 2320 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.
From the author: Indirect evidence of interindividual variation of the recombination fraction is considerable, but as yet direct evidence is lacking. Such interindividual variation could explain the widely observed gametic association in the major histocompatibility complex (MHC) region. A possible approach to this is the application of the polymerase chain reaction to closely linked markers on individual...
|
|