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Current insights into the mechanism of mammalian immunoglobulin class switch recombination

机译:目前对哺乳动物免疫球蛋白阶级开关重组机制的见解

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摘要

Immunoglobulin (Ig) class switch recombination (CSR) is the gene rearrangement process by which B lymphocytes change the Ig heavy chain constant region to permit a switch of Ig Isotype from IgM to IgG, IgA, or IgE. At the DNA level, CSR occurs via generation and joining of DNA double strand breaks (DSBs) at intronic switch regions located just upstream of each of the heavy chain constant regions. Activation-Induced deaminase (AID), a B cell specific enzyme, catalyzes cytosine deaminations (converting cytosines to uracils) as the initial DNA lesions that eventually lead to DSBs and CSR. Progress on AID structure integrates very well with knowledge about Ig class switch region nucleic acid structures that are supported by functional studies. It is an ideal time to review what is known about the mechanism of Ig CSR and its relation to somatic hypermutatlon. There have been many comprehensive reviews on various aspects of the CSR reaction and regulation of AID expression and activity. This review is focused on the relation between AID and switch region nucleic acid structures, with a particular emphasis on R-loops.
机译:免疫球蛋白(IG)阶级开关重组(CSR)是B淋巴细胞改变IG重链恒定区的基因重排过程,以允许将Ig同学与IgG,IgA或IgE的开关切换。在DNA水平中,CSR通过在位于每个重链恒定区域的上游的内肠开关区域的DNA双链断裂(DSB)的产生和连接发生。活化诱导的脱氨酶(AID),B细胞特异性酶,催化胞嘧啶脱胺(将胞嘧啶转化为URACIL),作为最终导致DSB和CSR的初始DNA病变。援助结构的进展非常良好地与功能研究支持的IG类开关区域核酸结构相结合。这是回顾IG CSR机制的理想时间及其与体细胞高乳房的关系。关于CSR反应的各个方面以及援助表达和活性的调节有许多全面评价。本综述专注于辅助和开关区域核酸结构之间的关系,特别强调R-环。

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