• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

PARP1 通过 PAR 化 GCN5 将其募集到 DSBs 处,促进 HR 和 NHEJ 修复。

PARylation of GCN5 by PARP1 mediates its recruitment to DSBs and facilitates both HR and NHEJ Repair.

机构信息

Shilpee Dutt Laboratory, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre, Navi Mumbai, 410210, India.

Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai, 400085, India.

出版信息

Cell Mol Life Sci. 2024 Nov 7;81(1):446. doi: 10.1007/s00018-024-05469-9.

DOI:10.1007/s00018-024-05469-9
PMID:39508866
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11544116/
Abstract

Efficient DNA double strand break (DSB) repair is necessary for genomic stability and determines efficacy of DNA damaging cancer therapeutics. Spatiotemporal dynamics and post-translational modifications of repair proteins at DSBs dictate repair efficacy. Here, we identified a non-canonical function of GCN5 in regulating both HR and NHEJ repair post genotoxic stress. Mechanistically, genotoxic stress induced GCN5 recruitment to DSBs. GCN5 PARylation by PARP1 was essential for its recruitment, acetyltransferase activity and DSB repair function. Liquid chromatography-mass spectrometry (LC-MS) identified DNA-PKcs as part of GCN5 interactome. In-vitro acetyltransferase assays revealed that GCN5 acetylates DNA-PKcs at K3241 residue, a prerequisite for DNA-PKcs S2056 phosphorylation and DSB recruitment. Alongside, ChIP-qPCR revealed GCN5 mediates transcription of PRKDC via H3K27Ac acetylation in its promoter region (- 710 to - 554). Genetic perturbation of GCN5 also decreased CHEK1, NBN1, TP53BP1, POL-L transcription and abrogated ATM, BRCA1 activation. Accordingly, GCN5 loss led to persistent ɣ-H2AX foci formation, compromised in-vivo HR-NHEJ and caused GBM radio-sensitization. Importantly, PARP1 inhibition phenocopied GCN5 loss. Together, this study identifies an untraversed DSB repair function of GCN5 and provides mechanistic insights into transcriptional as well as post-translational regulation of pivotal HR-NHEJ factors. Alongside, it highlights the translational importance of PARP1-GCN5 axis in mediating GBM radio-resistance.

摘要

高效的 DNA 双链断裂 (DSB) 修复对于基因组稳定性至关重要,决定了 DNA 损伤癌症治疗的疗效。修复蛋白在 DSB 处的时空动力学和翻译后修饰决定了修复效率。在这里,我们发现了 GCN5 在基因毒性应激后调节同源重组 (HR) 和非同源末端连接 (NHEJ) 修复的非典型功能。在机制上,基因毒性应激诱导 GCN5 募集到 DSB 。PARP1 对 GCN5 的 PAR 化对于其募集、乙酰转移酶活性和 DSB 修复功能是必不可少的。液相色谱-质谱 (LC-MS) 鉴定了 DNA-PKcs 是 GCN5 相互作用组的一部分。体外乙酰转移酶实验表明,GCN5 在 K3241 残基上将 DNA-PKcs 乙酰化,这是 DNA-PKcs S2056 磷酸化和 DSB 募集的前提。与此同时,ChIP-qPCR 显示 GCN5 通过其启动子区域(-710 至-554)中的 H3K27Ac 乙酰化来介导 PRKDC 的转录。GCN5 的遗传扰动也降低了 CHEK1、NBN1、TP53BP1、POL-L 的转录,并阻断了 ATM、BRCA1 的激活。因此,GCN5 的缺失导致持续形成 γ-H2AX 焦点,体内 HR-NHEJ 受损,并导致 GBM 放射增敏。重要的是,PARP1 抑制可模拟 GCN5 的缺失。总之,这项研究确定了 GCN5 未被探索的 DSB 修复功能,并为 HR-NHEJ 关键因子的转录和翻译后调控提供了机制见解。此外,它强调了 PARP1-GCN5 轴在介导 GBM 放射抗性中的翻译重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/aed75e2dd334/18_2024_5469_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/83faccd0a11b/18_2024_5469_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/785476e9a23e/18_2024_5469_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/4a2511b85a98/18_2024_5469_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/401039215711/18_2024_5469_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/ce852c803bf8/18_2024_5469_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/70de3f159f02/18_2024_5469_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/321fd8bbd147/18_2024_5469_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/aed75e2dd334/18_2024_5469_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/83faccd0a11b/18_2024_5469_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/785476e9a23e/18_2024_5469_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/4a2511b85a98/18_2024_5469_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/401039215711/18_2024_5469_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/ce852c803bf8/18_2024_5469_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/70de3f159f02/18_2024_5469_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/321fd8bbd147/18_2024_5469_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cb/11544116/aed75e2dd334/18_2024_5469_Fig8_HTML.jpg

相似文献

1
PARylation of GCN5 by PARP1 mediates its recruitment to DSBs and facilitates both HR and NHEJ Repair.PARP1 通过 PAR 化 GCN5 将其募集到 DSBs 处,促进 HR 和 NHEJ 修复。
Cell Mol Life Sci. 2024 Nov 7;81(1):446. doi: 10.1007/s00018-024-05469-9.
2
Common and unique genetic interactions of the poly(ADP-ribose) polymerases PARP1 and PARP2 with DNA double-strand break repair pathways.聚(ADP-核糖)聚合酶PARP1和PARP2与DNA双链断裂修复途径的常见和独特遗传相互作用。
DNA Repair (Amst). 2016 Sep;45:56-62. doi: 10.1016/j.dnarep.2016.06.001. Epub 2016 Jun 16.
3
GCN5 mediates DNA-PKcs crotonylation for DNA double-strand break repair and determining cancer radiosensitivity.GCN5 介导 DNA-PKcs 的克罗顿化以修复 DNA 双链断裂并决定癌症的放射敏感性。
Br J Cancer. 2024 Jun;130(10):1621-1634. doi: 10.1038/s41416-024-02636-4. Epub 2024 Apr 4.
4
Sp1-dependent recruitment of the histone acetylase p300 to DSBs facilitates chromatin remodeling and recruitment of the NHEJ repair factor Ku70.Sp1 依赖性募集组蛋白乙酰转移酶 p300 到 DSBs 促进染色质重塑和 NHEJ 修复因子 Ku70 的募集。
DNA Repair (Amst). 2021 Sep;105:103171. doi: 10.1016/j.dnarep.2021.103171. Epub 2021 Jul 7.
5
Histone deacetylase inhibitors decrease NHEJ both by acetylation of repair factors and trapping of PARP1 at DNA double-strand breaks in chromatin.组蛋白去乙酰化酶抑制剂通过修复因子的乙酰化作用以及在染色质中DNA双链断裂处捕获PARP1来减少非同源末端连接。
Leuk Res. 2016 Jun;45:14-23. doi: 10.1016/j.leukres.2016.03.007. Epub 2016 Mar 30.
6
DNA repair kinetics in SCID mice Sertoli cells and DNA-PKcs-deficient mouse embryonic fibroblasts.重症联合免疫缺陷(SCID)小鼠支持细胞和DNA依赖蛋白激酶催化亚基(DNA-PKcs)缺陷型小鼠胚胎成纤维细胞中的DNA修复动力学
Chromosoma. 2017 Mar;126(2):287-298. doi: 10.1007/s00412-016-0590-9. Epub 2016 May 2.
7
CTCF facilitates DNA double-strand break repair by enhancing homologous recombination repair.CTCF 通过增强同源重组修复来促进 DNA 双链断裂修复。
Sci Adv. 2017 May 24;3(5):e1601898. doi: 10.1126/sciadv.1601898. eCollection 2017 May.
8
Parp1-XRCC1 and the repair of DNA double strand breaks in mouse round spermatids.PARP1-XRCC1 与 DNA 双链断裂在小鼠圆形精子细胞中的修复。
Mutat Res. 2010 Jan 5;683(1-2):84-90. doi: 10.1016/j.mrfmmm.2009.10.011.
9
Analysis of chromatid-break-repair detects a homologous recombination to non-homologous end-joining switch with increasing load of DNA double-strand breaks.分析着丝粒断裂修复检测到同源重组向非同源末端连接的转换,这种转换随着 DNA 双链断裂负荷的增加而增加。
Mutat Res Genet Toxicol Environ Mutagen. 2021 Jul;867:503372. doi: 10.1016/j.mrgentox.2021.503372. Epub 2021 Jun 12.
10
Synergistic Roles of Non-Homologous End Joining and Homologous Recombination in Repair of Ionizing Radiation-Induced DNA Double Strand Breaks in Mouse Embryonic Stem Cells.非同源末端连接和同源重组在修复小鼠胚胎干细胞中电离辐射诱导的 DNA 双链断裂中的协同作用。
Cells. 2024 Aug 30;13(17):1462. doi: 10.3390/cells13171462.

引用本文的文献

1
Establishment and transcriptomic characteristics of radio-resistant meningioma cell lines.放射性抗性脑膜瘤细胞系的建立及其转录组特征
J Neurooncol. 2025 May;173(1):105-119. doi: 10.1007/s11060-025-04966-6. Epub 2025 Feb 28.

本文引用的文献

1
The novel Plasmodium berghei protein S14 is essential for sporozoite gliding motility and infectivity.新型伯氏疟原虫蛋白 S14 对子孢子的滑行运动和感染力是必需的。
J Cell Sci. 2024 Jun 1;137(11). doi: 10.1242/jcs.261857. Epub 2024 Jun 7.
2
GCN5 mediates DNA-PKcs crotonylation for DNA double-strand break repair and determining cancer radiosensitivity.GCN5 介导 DNA-PKcs 的克罗顿化以修复 DNA 双链断裂并决定癌症的放射敏感性。
Br J Cancer. 2024 Jun;130(10):1621-1634. doi: 10.1038/s41416-024-02636-4. Epub 2024 Apr 4.
3
DNA-PKcs-mediated transcriptional regulation of TOP2B drives chemoresistance in acute myeloid leukemia.
DNA依赖蛋白激酶催化亚基(DNA-PKcs)介导的拓扑异构酶IIβ(TOP2B)转录调控驱动急性髓系白血病的化疗耐药。
J Cell Sci. 2024 Feb 1;137(3). doi: 10.1242/jcs.261931. Epub 2024 Feb 13.
4
Histone acetyltransferase Gcn5-mediated histone H3 acetylation facilitates cryptococcal morphogenesis and sexual reproduction.组蛋白乙酰转移酶 Gcn5 介导的组蛋白 H3 乙酰化促进隐球菌形态发生和有性生殖。
mSphere. 2023 Dec 20;8(6):e0029923. doi: 10.1128/msphere.00299-23. Epub 2023 Oct 18.
5
Emerging role of GCN5 in human diseases and its therapeutic potential.GCN5 在人类疾病中的新兴作用及其治疗潜力。
Biomed Pharmacother. 2023 Sep;165:114835. doi: 10.1016/j.biopha.2023.114835. Epub 2023 Jun 21.
6
Characterization of Chromosomal Instability in Glioblastoma.胶质母细胞瘤中染色体不稳定性的特征分析
Front Genet. 2022 Jan 28;12:810793. doi: 10.3389/fgene.2021.810793. eCollection 2021.
7
DUSP6 regulates radiosensitivity in glioblastoma by modulating the recruitment of phosphorylated DNAPKcs at DNA double-strand breaks.DUSP6 通过调节 DNA 双链断裂处磷酸化的 DNAPKcs 的募集来调节胶质母细胞瘤的放射敏感性。
J Cell Sci. 2021 Dec 15;134(24). doi: 10.1242/jcs.259520.
8
DNA Repair Pathways in Cancer Therapy and Resistance.癌症治疗与耐药中的DNA修复途径
Front Pharmacol. 2021 Feb 8;11:629266. doi: 10.3389/fphar.2020.629266. eCollection 2020.
9
Transcriptional Activation of MYC-Induced Genes by GCN5 Promotes B-cell Lymphomagenesis.GCN5 转录激活 MYC 诱导基因促进 B 细胞淋巴瘤的发生。
Cancer Res. 2020 Dec 15;80(24):5543-5553. doi: 10.1158/0008-5472.CAN-20-2379. Epub 2020 Nov 9.
10
Elevated GCN5 expression confers tamoxifen resistance by upregulating AIB1 expression in ER-positive breast cancer.GCN5 表达升高通过上调 ER 阳性乳腺癌中的 AIB1 表达赋予他莫昔芬耐药性。
Cancer Lett. 2020 Dec 28;495:145-155. doi: 10.1016/j.canlet.2020.09.017. Epub 2020 Sep 25.