IgH Chain Class Switch Recombination: Mechanism and Regulation

被引:184
|
作者
Stavnezer, Janet [1 ]
Schrader, Carol E. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA 01605 USA
来源
JOURNAL OF IMMUNOLOGY | 2014年 / 193卷 / 11期
基金
美国国家卫生研究院;
关键词
INDUCED CYTIDINE DEAMINASE; RNA-POLYMERASE-II; ACTIVATION-INDUCED DEAMINASE; DOUBLE-STRAND BREAKS; B-CELL DIFFERENTIATION; ANTIBODY CLASS SWITCH; END-JOINING PATHWAYS; C-TERMINAL REGION; SOMATIC HYPERMUTATION; DNA BREAKS;
D O I
10.4049/jimmunol.1401849
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:5370 / 5378
页数:9
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