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V H5 中协调的突变和体细胞高频突变的进化。

Evolution of coordinated mutagenesis and somatic hypermutation in VH5.

机构信息

Division of Biological Sciences, The University of Montana, Missoula, MT 59812, USA.

出版信息

Mol Immunol. 2011 Dec;49(3):537-48. doi: 10.1016/j.molimm.2011.10.001. Epub 2011 Nov 5.

Abstract

The VH5 human antibody gene was analyzed using a computer program (mfg) which simulates transcription, to better understand transcription-driven mutagenesis events that occur during "phase 1" of somatic hypermutation. Results show that the great majority of mutations in the non-transcribed strand occur within loops of two predicted high-stability stem-loop structures, termed SLSs 14.9 and 13.9. In fact, 89% of the 2505 mutations reported are within the encoded complementarity-determining region (CDR) and occur in loops of these high-stability structures. In vitro studies were also done and verified the existence of SLS 14.9. Following the formation of SLSs 14.9 and 13.9, a sustained period of transcriptional activity occurs within a window size of 60-70 nucleotides. During this period, the stability of these two SLSs does not change, and may provide the substrate for base exchanges and mutagenesis. The data suggest that many mutable bases are exposed simultaneously at pause sites, allowing for coordinated mutagenesis.

摘要

使用计算机程序(mfg)对 VH5 人抗体基因进行分析,以更好地理解在体细胞高频突变的“第 1 阶段”发生的转录驱动突变事件。结果表明,在非转录链上的大多数突变发生在两个预测的高稳定性茎环结构(称为 SLSs 14.9 和 13.9)的环内。事实上,报告的 2505 个突变中的 89%位于编码的互补决定区(CDR)内,发生在这些高稳定性结构的环中。体外研究也证实了 SLS 14.9 的存在。形成 SLSs 14.9 和 13.9 后,在 60-70 个核苷酸大小的窗口内会发生持续的转录活性。在此期间,这两个 SLS 的稳定性不会改变,并且可能为碱基交换和突变提供底物。数据表明,许多易变碱基同时在暂停位点暴露,从而允许协调突变。

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