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免疫球蛋白体细胞超突变

Immunoglobulin somatic hypermutation.

作者信息

Teng Grace, Papavasiliou F Nina

机构信息

Laboratory of Lymphocyte Biology, The Rockefeller University, New York, NY 10021, USA.

出版信息

Annu Rev Genet. 2007;41:107-20. doi: 10.1146/annurev.genet.41.110306.130340.

Abstract

The immunoglobulin (Ig) repertoire achieves functional diversification through several somatic alterations of the Ig locus. One of these processes, somatic hypermutation (SHM), deposits point mutations into the variable region of the Ig gene to generate higher-affinity variants. Activation-induced cytidine deaminase (AID) converts cytidine to uridine to initiate the hypermutation process. Error-prone versions of DNA repair are believed to then process these lesions into a diverse spectrum of point mutations. We review the current understanding of the molecular mechanisms and regulation of SHM, and also discuss emerging ideas which merit further exploration.

摘要

免疫球蛋白(Ig)库通过Ig基因座的几种体细胞改变实现功能多样化。这些过程之一,即体细胞高频突变(SHM),将点突变沉积到Ig基因的可变区以产生高亲和力变体。激活诱导的胞苷脱氨酶(AID)将胞苷转化为尿苷以启动高频突变过程。据信易出错的DNA修复版本随后将这些损伤加工成各种各样的点突变。我们综述了目前对SHM分子机制和调控的理解,并讨论了值得进一步探索的新观点。

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