AID targeting is dependent on RNA polymerase II pausing

被引:33
|
作者
Kenter, Amy L. [1 ]
机构
[1] Univ Illinois, Coll Med, Dept Microbiol & Immunol, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
AID targeting; Germline transcription; Epigenetic modifications; RNA polymerase II pausing; INDUCED CYTIDINE DEAMINASE; CLASS SWITCH RECOMBINATION; TRACT-BINDING-PROTEIN; SOMATIC HYPERMUTATION; TRANSCRIPTION ELONGATION; B-CELLS; HISTONE ACETYLATION; R-LOOPS; IMMUNOGLOBULIN GENES; VARIABLE REGION;
D O I
10.1016/j.smim.2012.06.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activation induced deaminase (AID) is globally targeted to immunoglobulin loci, preferentially focused to switch (S) regions and variable (V) regions, and prone to attack hotspot motifs. Nevertheless, AID deamination is not exclusive to Ig loci and the rules regulating AID targeting remain unclear. Transcription is critically required for class switch recombination and somatic hypermutation. Here, I consider the unique features associated with S region transcription leading to RNA polymerase II pausing, that in turn promote the introduction of activating chromatin remodeling, histone modifications and recruitment of AID to targeted S regions. These findings allow for a better understanding of the interplay between transcription, AID targeting and mistargeting to Ig and non-Ig loci. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:281 / 286
页数:6
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