Show simple item record

dc.contributor.authorStavnezer, Janet
dc.contributor.authorSchrader, Carol E.
dc.date2022-08-11T08:08:32.000
dc.date.accessioned2022-08-23T15:58:10Z
dc.date.available2022-08-23T15:58:10Z
dc.date.issued2014-12-01
dc.date.submitted2015-05-29
dc.identifier.citationJ 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.issn0022-1767 (Linking)
dc.identifier.doi10.4049/jimmunol.1401849
dc.identifier.pmid25411432
dc.identifier.urihttp://hdl.handle.net/20.500.14038/30373
dc.description.abstractIgH 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.isoen_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.urlhttp://dx.doi.org/10.4049/jimmunol.1401849
dc.subjectAnimals
dc.subjectB-Lymphocytes
dc.subjectCytidine Deaminase
dc.subjectDNA Repair
dc.subjectHumans
dc.subject*Immunoglobulin Class Switching
dc.subjectImmunoglobulin Heavy Chains
dc.subjectLymphocyte Activation
dc.subjectCellular and Molecular Physiology
dc.subjectImmunity
dc.titleIgH chain class switch recombination: mechanism and regulation
dc.typeJournal Article
dc.source.journaltitleJournal of immunology (Baltimore, Md. : 1950)
dc.source.volume193
dc.source.issue11
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/645
dc.identifier.contextkey7158524
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.submissionpathfaculty_pubs/645
dc.contributor.departmentDepartment of Microbiology and Physiological Systems
dc.source.pages5370-8


This item appears in the following Collection(s)

Show simple item record