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Transcriptional stalling in B-lymphocytesA mechanism for antibody diversification and maintenance of genomic integrity

机译:B淋巴细胞中的转录停滞抗体多样化和维持基因组完整性的机制

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摘要

B cells utilize three DNA alteration strategies—V(D)J recombination, somatic hypermutation (SHM) and class switch recombination (CSR)—to somatically mutate their genome, thereby expressing a plethora of antibodies tailor-made against the innumerableantigens they encounter while in circulation. Of these three events, the single-strand DNA cytidine deaminase, Activation Induced cytidine Deaminase (AID), is responsible for SHM and CSR. Recent advances, discussed in this review article, point toward various components of RNA polymerase II "stalling" machinery as regulators of AID activity during antibody diversification and maintenance of B cell genome integrity.
机译:B细胞利用三种DNA改变策略-V(D)J重组,体细胞超突变(SHM)和类别开关重组(CSR)-来使它们的基因组发生体细胞突变,从而表达针对它们在体内遇到的无数抗原量身定制的大量抗体。循环。在这三个事件中,单链DNA胞嘧啶脱氨酶即激活诱导的胞苷脱氨酶(AID)负责SHM和CSR。在这篇综述文章中讨论的最新进展指出,RNA聚合酶II“停滞”机制的各种组成部分在抗体多样化和B细胞基因组完整性维持过程中作为AID活性的调节剂。

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