Yabuki Munehisa, Fujii Monica M, Maizels Nancy
Department of Immunology, University of Washington School of Medicine, Seattle, Washington 98195-7650, USA.
Nat Immunol. 2005 Jul;6(7):730-6. doi: 10.1038/ni1215. Epub 2005 Jun 5.
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.
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。