IgH chain class switch recombination: mechanism and regulation
dc.contributor.author | Stavnezer, Janet | |
dc.contributor.author | Schrader, Carol E. | |
dc.date | 2022-08-11T08:08:32.000 | |
dc.date.accessioned | 2022-08-23T15:58:10Z | |
dc.date.available | 2022-08-23T15:58:10Z | |
dc.date.issued | 2014-12-01 | |
dc.date.submitted | 2015-05-29 | |
dc.identifier.citation | J Immunol. 2014 Dec 1;193(11):5370-8. doi: 10.4049/jimmunol.1401849. <a href="http://dx.doi.org/10.4049/jimmunol.1401849">Link to article on publisher's site</a> | |
dc.identifier.issn | 0022-1767 (Linking) | |
dc.identifier.doi | 10.4049/jimmunol.1401849 | |
dc.identifier.pmid | 25411432 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/30373 | |
dc.description.abstract | IgH class switching occurs rapidly after activation of mature naive B cells, resulting in a switch from expression of IgM and IgD to expression of IgG, IgE, or IgA; this switch improves the ability of Abs to remove the pathogen that induces the humoral immune response. Class switching occurs by a deletional recombination between two switch regions, each of which is associated with a H chain constant region gene. Class switch recombination (CSR) is instigated by activation-induced cytidine deaminase, which converts cytosines in switch regions to uracils. The uracils are subsequently removed by two DNA-repair pathways, resulting in mutations, single-strand DNA breaks, and the double-strand breaks required for CSR. We discuss several aspects of CSR, including how CSR is induced, CSR in B cell progenitors, the roles of transcription and chromosomal looping in CSR, and the roles of certain DNA-repair enzymes in CSR. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=25411432&dopt=Abstract">Link to Article in PubMed</a> | |
dc.relation.url | http://dx.doi.org/10.4049/jimmunol.1401849 | |
dc.subject | Animals | |
dc.subject | B-Lymphocytes | |
dc.subject | Cytidine Deaminase | |
dc.subject | DNA Repair | |
dc.subject | Humans | |
dc.subject | *Immunoglobulin Class Switching | |
dc.subject | Immunoglobulin Heavy Chains | |
dc.subject | Lymphocyte Activation | |
dc.subject | Cellular and Molecular Physiology | |
dc.subject | Immunity | |
dc.title | IgH chain class switch recombination: mechanism and regulation | |
dc.type | Journal Article | |
dc.source.journaltitle | Journal of immunology (Baltimore, Md. : 1950) | |
dc.source.volume | 193 | |
dc.source.issue | 11 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/faculty_pubs/645 | |
dc.identifier.contextkey | 7158524 | |
html.description.abstract | <p>IgH class switching occurs rapidly after activation of mature naive B cells, resulting in a switch from expression of IgM and IgD to expression of IgG, IgE, or IgA; this switch improves the ability of Abs to remove the pathogen that induces the humoral immune response. Class switching occurs by a deletional recombination between two switch regions, each of which is associated with a H chain constant region gene. Class switch recombination (CSR) is instigated by activation-induced cytidine deaminase, which converts cytosines in switch regions to uracils. The uracils are subsequently removed by two DNA-repair pathways, resulting in mutations, single-strand DNA breaks, and the double-strand breaks required for CSR. We discuss several aspects of CSR, including how CSR is induced, CSR in B cell progenitors, the roles of transcription and chromosomal looping in CSR, and the roles of certain DNA-repair enzymes in CSR.</p> | |
dc.identifier.submissionpath | faculty_pubs/645 | |
dc.contributor.department | Department of Microbiology and Physiological Systems | |
dc.source.pages | 5370-8 |