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MRE11-RAD50-NBS1复合物可加速免疫球蛋白可变区的体细胞高频突变和基因转换。

The MRE11-RAD50-NBS1 complex accelerates somatic hypermutation and gene conversion of immunoglobulin variable regions.

作者信息

Yabuki Munehisa, Fujii Monica M, Maizels Nancy

机构信息

Department of Immunology, University of Washington School of Medicine, Seattle, Washington 98195-7650, USA.

出版信息

Nat Immunol. 2005 Jul;6(7):730-6. doi: 10.1038/ni1215. Epub 2005 Jun 5.

Abstract

Targeted diversification of immunoglobulin variable regions is induced by activation-induced deaminase and may occur by either somatic hypermutation or gene conversion. MRE11-RAD50-NBS1 (MRN) is a ubiquitous and conserved nuclease complex critical for DNA break repair and is essential in class-switch recombination. Here we show that ectopic expression of NBS1, the regulatory subunit of MRN, accelerated hypermutation in the human B cell line Ramos and accelerated gene conversion in the chicken B cell line DT40. In both cases, accelerated diversification depended on MRN complex formation. These data suggest that MRN promotes DNA cleavage and/or mutagenic repair of lesions initiated by activation-induced deaminase, acting in the shared pathway of immunoglobulin gene diversification.

摘要

免疫球蛋白可变区的靶向多样化由激活诱导的脱氨酶诱导,可能通过体细胞超突变或基因转换发生。MRE11-RAD50-NBS1(MRN)是一种普遍存在且保守的核酸酶复合物,对DNA断裂修复至关重要,在类别转换重组中必不可少。在这里,我们表明MRN的调节亚基NBS1的异位表达加速了人B细胞系Ramos中的超突变,并加速了鸡B细胞系DT40中的基因转换。在这两种情况下,加速的多样化都依赖于MRN复合物的形成。这些数据表明,MRN促进由激活诱导的脱氨酶引发的损伤的DNA切割和/或诱变修复,作用于免疫球蛋白基因多样化的共同途径。

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