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Senataxin 和 RNase H2 冗余性地发挥作用,以抑制类别转换重组过程中的基因组不稳定性。

Senataxin and RNase H2 act redundantly to suppress genome instability during class switch recombination.

机构信息

Department of Microbiology and Molecular Genetics, University of California, Davis, Davis, United States.

Department of Molecular and Cellular Biology, University of California, Davis, Davis, United States.

出版信息

Elife. 2022 Dec 21;11:e78917. doi: 10.7554/eLife.78917.

Abstract

Class switch recombination generates distinct antibody isotypes critical to a robust adaptive immune system, and defects are associated with autoimmune disorders and lymphomagenesis. Transcription is required during class switch recombination to recruit the cytidine deaminase AID-an essential step for the formation of DNA double-strand breaks-and strongly induces the formation of R loops within the immunoglobulin heavy-chain locus. However, the impact of R loops on double-strand break formation and repair during class switch recombination remains unclear. Here, we report that cells lacking two enzymes involved in R loop removal-senataxin and RNase H2-exhibit increased R loop formation and genome instability at the immunoglobulin heavy-chain locus without impacting its transcriptional activity, AID recruitment, or class switch recombination efficiency. Senataxin and RNase H2-deficient cells also exhibit increased insertion mutations at switch junctions, a hallmark of alternative end joining. Importantly, these phenotypes were not observed in cells lacking senataxin or RNase H2B alone. We propose that senataxin acts redundantly with RNase H2 to mediate timely R loop removal, promoting efficient repair while suppressing AID-dependent genome instability and insertional mutagenesis.

摘要

类别转换重组产生了不同的抗体同种型,这对强大的适应性免疫系统至关重要,而缺陷与自身免疫疾病和淋巴瘤的发生有关。类别转换重组过程中需要转录来招募胞嘧啶脱氨酶 AID——这是形成 DNA 双链断裂的必要步骤——并在免疫球蛋白重链基因座内强烈诱导 R 环的形成。然而,R 环对类别转换重组过程中双链断裂的形成和修复的影响仍不清楚。在这里,我们报告说,缺乏两种参与 R 环去除的酶——senataxin 和 RNase H2 的细胞在不影响其转录活性、AID 募集或类别转换重组效率的情况下,在免疫球蛋白重链基因座中表现出增加的 R 环形成和基因组不稳定性。senataxin 和 RNase H2 缺陷细胞在转换连接处也表现出增加的插入突变,这是替代末端连接的标志。重要的是,在单独缺乏 senataxin 或 RNase H2B 的细胞中没有观察到这些表型。我们提出,senataxin 与 RNase H2 冗余地作用以介导及时的 R 环去除,促进有效的修复,同时抑制 AID 依赖性基因组不稳定性和插入突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e57/9771370/1800a05f6b00/elife-78917-fig1.jpg

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