Suppr超能文献

AID 诱导的拓扑异构酶 1 减少导致 DNA 结构改变和 DNA 断裂,从而促进类别转换重组。

AID-induced decrease in topoisomerase 1 induces DNA structural alteration and DNA cleavage for class switch recombination.

机构信息

Department of Immunology and Genomic Medicine, Graduate School of Medicine, Kyoto University, Yoshida Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22375-80. doi: 10.1073/pnas.0911879106. Epub 2009 Dec 11.

Abstract

To initiate class switch recombination (CSR) activation-induced cytidine deaminase (AID) induces staggered nick cleavage in the S region, which lies 5' to each Ig constant region gene and is rich in palindromic sequences. Topoisomerase 1 (Top1) controls the supercoiling of DNA by nicking, rotating, and religating one strand of DNA. Curiously, Top1 reduction or AID overexpression causes the genomic instability. Here, we report that the inactivation of Top1 by its specific inhibitor camptothecin drastically blocked both the S region cleavage and CSR, indicating that Top1 is responsible for the S region cleavage in CSR. Surprisingly, AID expression suppressed Top1 mRNA translation and reduced its protein level. In addition, the decrease in the Top1 protein by RNA-mediated knockdown augmented the AID-dependent S region cleavage, as well as CSR. Furthermore, Top1 reduction altered DNA structure of the Smu region. Taken together, AID-induced Top1 reduction alters S region DNA structure probably to non-B form, on which Top1 can introduce nicks but cannot religate, resulting in S region cleavage.

摘要

为了启动类别转换重组 (CSR),激活诱导的胞嘧啶脱氨酶 (AID) 在 S 区诱导交错的切口断裂,S 区位于每个 Ig 恒定区基因的 5'端,富含回文序列。拓扑异构酶 1 (Top1) 通过切口、旋转和重新连接一条 DNA 链来控制 DNA 的超螺旋。奇怪的是,Top1 的减少或 AID 的过表达导致基因组不稳定。在这里,我们报告说,其特异性抑制剂喜树碱使 Top1 失活,可大大阻断 S 区的切割和 CSR,表明 Top1 负责 CSR 中的 S 区切割。令人惊讶的是,AID 的表达抑制了 Top1 mRNA 的翻译并降低了其蛋白水平。此外,通过 RNA 介导的敲低减少 Top1 蛋白会增加 AID 依赖性 S 区切割和 CSR。此外,Top1 的减少改变了 Smu 区域的 DNA 结构。总之,AID 诱导的 Top1 减少改变了 S 区 DNA 结构,可能是非 B 形式,Top1 可以在其上引入切口但不能重新连接,导致 S 区切割。

相似文献

1
AID-induced decrease in topoisomerase 1 induces DNA structural alteration and DNA cleavage for class switch recombination.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22375-80. doi: 10.1073/pnas.0911879106. Epub 2009 Dec 11.
2
Decrease in topoisomerase I is responsible for activation-induced cytidine deaminase (AID)-dependent somatic hypermutation.
Proc Natl Acad Sci U S A. 2011 Nov 29;108(48):19305-10. doi: 10.1073/pnas.1114522108. Epub 2011 Nov 11.
4
Ago2 and a miRNA reduce Topoisomerase 1 for enhancing DNA cleavage in antibody diversification by activation-induced cytidine deaminase.
Proc Natl Acad Sci U S A. 2023 May 2;120(18):e2216918120. doi: 10.1073/pnas.2216918120. Epub 2023 Apr 24.
5
Topoisomerase I deficiency causes RNA polymerase II accumulation and increases AID abundance in immunoglobulin variable genes.
DNA Repair (Amst). 2015 Jun;30:46-52. doi: 10.1016/j.dnarep.2015.03.004. Epub 2015 Mar 18.
7
Single-strand DNA breaks in Ig class switch recombination that depend on UNG but not AID.
Int Immunol. 2008 Nov;20(11):1381-93. doi: 10.1093/intimm/dxn097. Epub 2008 Sep 15.
9
Splicing regulator SRSF1-3 that controls somatic hypermutation of IgV genes interacts with topoisomerase 1 and AID.
Mol Immunol. 2019 Dec;116:63-72. doi: 10.1016/j.molimm.2019.10.002. Epub 2019 Oct 15.

引用本文的文献

1
G-quadruplexes on chromosomal DNA negatively regulates topoisomerase 1 activity.
Nucleic Acids Res. 2024 Mar 21;52(5):2142-2156. doi: 10.1093/nar/gkae073.
3
Ago2 and a miRNA reduce Topoisomerase 1 for enhancing DNA cleavage in antibody diversification by activation-induced cytidine deaminase.
Proc Natl Acad Sci U S A. 2023 May 2;120(18):e2216918120. doi: 10.1073/pnas.2216918120. Epub 2023 Apr 24.
4
Topoisomerases in Immune Cell Development and Function.
J Immunol. 2023 Jan 15;210(2):126-133. doi: 10.4049/jimmunol.2200650.
6
Epigenetic reader SP140 loss of function drives Crohn's disease due to uncontrolled macrophage topoisomerases.
Cell. 2022 Aug 18;185(17):3232-3247.e18. doi: 10.1016/j.cell.2022.06.048. Epub 2022 Aug 10.
7
Molecular profiling of individual FDA-approved clinical drugs identifies modulators of nonsense-mediated mRNA decay.
Mol Ther Nucleic Acids. 2021 Dec 10;27:304-318. doi: 10.1016/j.omtn.2021.12.003. eCollection 2022 Mar 8.
9
RNA-binding motifs of hnRNP K are critical for induction of antibody diversification by activation-induced cytidine deaminase.
Proc Natl Acad Sci U S A. 2020 May 26;117(21):11624-11635. doi: 10.1073/pnas.1921115117. Epub 2020 May 8.

本文引用的文献

1
Apex2 is required for efficient somatic hypermutation but not for class switch recombination of immunoglobulin genes.
Int Immunol. 2009 Aug;21(8):947-55. doi: 10.1093/intimm/dxp061. Epub 2009 Jun 25.
3
Cdc2-like kinases and DNA topoisomerase I regulate alternative splicing of tissue factor in human endothelial cells.
Circ Res. 2009 Mar 13;104(5):589-99. doi: 10.1161/CIRCRESAHA.108.183905. Epub 2009 Jan 22.
4
Conformational variants of duplex DNA correlated with cytosine-rich chromosomal fragile sites.
J Biol Chem. 2009 Mar 13;284(11):7157-64. doi: 10.1074/jbc.M806866200. Epub 2008 Dec 23.
5
Mechanism and regulation of class switch recombination.
Annu Rev Immunol. 2008;26:261-92. doi: 10.1146/annurev.immunol.26.021607.090248.
6
Two levels of protection for the B cell genome during somatic hypermutation.
Nature. 2008 Feb 14;451(7180):841-5. doi: 10.1038/nature06547.
7
Mechanism of R-loop formation at immunoglobulin class switch sequences.
Mol Cell Biol. 2008 Jan;28(1):50-60. doi: 10.1128/MCB.01251-07. Epub 2007 Oct 22.
8
Nonclassic functions of human topoisomerase I: genome-wide and pharmacologic analyses.
Cancer Res. 2007 Sep 15;67(18):8752-61. doi: 10.1158/0008-5472.CAN-06-4554.
9
Sequence dependence of chromosomal R-loops at the immunoglobulin heavy-chain Smu class switch region.
Mol Cell Biol. 2007 Aug;27(16):5921-32. doi: 10.1128/MCB.00702-07. Epub 2007 Jun 11.
10
Non-B DNA conformations, mutagenesis and disease.
Trends Biochem Sci. 2007 Jun;32(6):271-8. doi: 10.1016/j.tibs.2007.04.003. Epub 2007 May 9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验