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Histone chaperone Spt6 is required for class switch recombination but not somatic hypermutation

机译:组开关重组需要组蛋白伴侣Spt6但体细胞超突变不是必需的

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摘要

Activation-induced cytidine deaminase (AID) is shown to be essential and sufficient to induce two genetic alterations in the Ig loci: class switch recombination (CSR) and somatic hypermutation (SHM). However, it is still unknown how a single-molecule AID differentially regulates CSR and SHM. Here we identified Spt6 as an AID-interacting protein by yeast two-hybrid screening and immunoprecipitation followed by mass spectrometry. Knockdown of Spt6 resulted in severe reduction of CSR in both the endogenous Ig locus in B cells and an artificial substrate in fibroblast cells. Conversely, knockdown of Spt6 did not reduce but slightly enhanced SHM in an artificial substrate in B cells, indicating that Spt6 is required for AID to induce CSR but not SHM. These results suggest that Spt6 is involved in differential regulation of CSR and SHM by AID.
机译:激活诱导的胞苷脱氨酶(AID)被证明是必需的,并且足以在Ig基因座中诱导两种遗传改变:类别开关重组(CSR)和体细胞超突变(SHM)。然而,仍然未知的是单分子AID如何差异调节CSR和SHM。在这里,我们通过酵母双杂交筛选和免疫沉淀,随后质谱鉴定出Spt6为AID相互作用蛋白。击倒Spt6会导致B细胞内源性Ig基因座和成纤维细胞中人工底物的CSR严重降低。相反,在B细胞的人工底物中,Spt6的敲低并没有降低SHM,但稍微增强了SHM,这表明AID诱导CSR而不是SHM需要Spt6。这些结果表明Spt6参与了AID对CSR和SHM的差异调节。

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