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染色质背景下的DNA错配修复

DNA mismatch repair in the context of chromatin.

作者信息

Huang Yaping, Li Guo-Min

机构信息

Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA.

出版信息

Cell Biosci. 2020 Feb 3;10:10. doi: 10.1186/s13578-020-0379-7. eCollection 2020.

DOI:10.1186/s13578-020-0379-7
PMID:32025281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6996186/
Abstract

DNA mismatch repair (MMR) maintains replication fidelity by correcting mispaired nucleotides incorporated by DNA polymerases. Defects in MMR lead to cancers characterized by microsatellite instability. Recently, chromatin mechanisms that regulate MMR have been discovered, which sheds new light on MMR deficiency and its role in tumorigenesis. This review summarizes these chromatin-level mechanisms that regulate MMR and their implications for tumor development.

摘要

DNA错配修复(MMR)通过校正DNA聚合酶掺入的错配核苷酸来维持复制保真度。MMR缺陷会导致以微卫星不稳定性为特征的癌症。最近,已发现调控MMR的染色质机制,这为MMR缺陷及其在肿瘤发生中的作用提供了新的线索。本综述总结了这些调控MMR的染色质水平机制及其对肿瘤发展的影响。

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本文引用的文献

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Chromatin remodeling and mismatch repair: Access and excision.染色质重塑和错配修复:进入和切除。
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Cancer-driving H3G34V/R/D mutations block H3K36 methylation and H3K36me3-MutSα interaction.致癌的 H3G34V/R/D 突变阻断 H3K36 甲基化和 H3K36me3-MutSα 相互作用。
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DNA mismatch repair preferentially safeguards actively transcribed genes.
用于儿童癌症的免疫检查点抑制剂:仍然处于僵局吗?
Pharmaceuticals (Basel). 2024 Jul 26;17(8):991. doi: 10.3390/ph17080991.
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Sumoylation participates in the regulation of YB-1-mediated mismatch repair deficiency and alkylator tolerance.SUMO化参与YB-1介导的错配修复缺陷和烷化剂耐受性的调控。
Am J Cancer Res. 2022 Dec 15;12(12):5462-5483. eCollection 2022.
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Research highlights on contributions of mitochondrial DNA microsatellite instability in solid cancers - an overview.实体癌中线粒体DNA微卫星不稳定性贡献的研究亮点——综述
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Pan-Cancer Transcriptomic Analysis Identifies PLK1 Crucial for the Tumorigenesis of Clear Cell Renal Cell Carcinoma.泛癌转录组分析确定PLK1对透明细胞肾细胞癌的肿瘤发生至关重要。
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Comprehensive Pan-Cancer Analysis and the Regulatory Mechanism of ASF1B, a Gene Associated With Thyroid Cancer Prognosis in the Tumor Micro-Environment.肿瘤微环境中与甲状腺癌预后相关基因ASF1B的综合泛癌分析及其调控机制
Front Oncol. 2021 Aug 20;11:711756. doi: 10.3389/fonc.2021.711756. eCollection 2021.
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DNA Mismatch Repair and its Role in Huntington's Disease.DNA 错配修复及其在亨廷顿病中的作用。
J Huntingtons Dis. 2021;10(1):75-94. doi: 10.3233/JHD-200438.
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Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.CAG/CTG 重复不稳定的修饰因子:来自哺乳动物模型的见解。
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Cancers (Basel). 2021 Jan 11;13(2):241. doi: 10.3390/cancers13020241.
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Inhibition of a K9/K36 demethylase by an H3.3 point mutation found in paediatric glioblastoma.在儿科脑胶质瘤中发现的 H3.3 点突变抑制了 K9/K36 去甲基酶。
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Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1.错配碱基对周围的核小体通过 Msh2 依赖性反应排除,该反应借助于 SNF2 家族 ATP 酶 Smarcad1。
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ARID1A deficiency promotes mutability and potentiates therapeutic antitumor immunity unleashed by immune checkpoint blockade.ARID1A 缺失可促进突变并增强免疫检查点阻断引发的抗肿瘤治疗性免疫。
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