Source:http://linkedlifedata.com/resource/pubmed/id/21056729
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2010-11-8
|
pubmed:abstractText |
Class switch recombination (CSR) is induced upon B cell activation and occurs within special DNA regions, termed switch (S) regions, which consist of tandem repeats of G-rich sequences. CSR occurs by introduction of double-strand breaks (DSBs) into each S region, and recombination by nonhomologous end-joining (NHEJ). The recombination event occurs during the G1 phase of the cell cycle in cells that are rapidly dividing. By examination of patients and mouse knock-out strains lacking various DNA-damage response factors and enzymes involved in DNA repair, much has been learned about which factors are important for CSR, how DSBs are introduced into S regions, and how the donor and acceptor S regions are then recombined. One of the approaches for analyzing the steps involved in CSR is to determine the nucleotide sequence of S-S junctions. Many of the DNA repair deficiencies alter the sequence of the recombination junctions, generally increasing the use of microhomologies, interpreted as a shift from classical (C)-NHEJ to alternative end-joining (A-EJ). However, it is clear that A-EJ, is not simply one pathway; rather, recombination is likely to occur using various subsets of end-joining factors, which will vary depending on the structure of the DSBs provided by the initial phases of CSR. Herein we review the results of analyses of S-S junctions, suggest minimal information required for these analyses, and attempt to integrate these results in order to increase our understanding of the complex process of CSR.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
1557-8445
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Inc. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
108
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
45-109
|
pubmed:meshHeading |
pubmed-meshheading:21056729-Animals,
pubmed-meshheading:21056729-B-Lymphocytes,
pubmed-meshheading:21056729-DNA Repair,
pubmed-meshheading:21056729-Humans,
pubmed-meshheading:21056729-Immunoglobulin Class Switching,
pubmed-meshheading:21056729-Immunoglobulin Isotypes,
pubmed-meshheading:21056729-Mice
|
pubmed:year |
2010
|
pubmed:articleTitle |
Mapping of switch recombination junctions, a tool for studying DNA repair pathways during immunoglobulin class switching.
|
pubmed:affiliation |
Department of Microbiology and Physiological Systems, Program in Immunology and Virology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
|
pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|