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本文引用的文献

1
Organizing DNA repair in the nucleus: DSBs hit the road.在细胞核中组织DNA修复:双链断裂踏上征程。
Curr Opin Cell Biol. 2017 Jun;46:1-8. doi: 10.1016/j.ceb.2016.12.003. Epub 2017 Jan 6.
2
Persistent nuclear actin filaments inhibit transcription by RNA polymerase II.持续存在的核肌动蛋白丝会抑制RNA聚合酶II的转录。
J Cell Sci. 2016 Sep 15;129(18):3412-25. doi: 10.1242/jcs.195867. Epub 2016 Aug 2.
3
High Expression of XRCC6 Promotes Human Osteosarcoma Cell Proliferation through the β-Catenin/Wnt Signaling Pathway and Is Associated with Poor Prognosis.XRCC6的高表达通过β-连环蛋白/ Wnt信号通路促进人骨肉瘤细胞增殖并与不良预后相关。
Int J Mol Sci. 2016 Jul 22;17(7):1188. doi: 10.3390/ijms17071188.
4
A Role for Nuclear Actin in HDAC 1 and 2 Regulation.核肌动蛋白在组蛋白去乙酰化酶 1 和 2 调控中的作用。
Sci Rep. 2016 Jun 27;6:28460. doi: 10.1038/srep28460.
5
LIG4 mediates Wnt signalling-induced radioresistance.LIG4介导Wnt信号通路诱导的放射抗性。
Nat Commun. 2016 Mar 24;7:10994. doi: 10.1038/ncomms10994.
6
Nuclear F-actin enhances the transcriptional activity of β-catenin by increasing its nuclear localization and binding to chromatin.核内丝状肌动蛋白通过增加β-连环蛋白的核定位及与染色质的结合来增强其转录活性。
Histochem Cell Biol. 2016 Apr;145(4):389-99. doi: 10.1007/s00418-016-1416-9. Epub 2016 Feb 22.
7
Beyond β-catenin: prospects for a larger catenin network in the nucleus.超越β-连环蛋白:细胞核中更大连环蛋白网络的前景。
Nat Rev Mol Cell Biol. 2016 Jan;17(1):55-64. doi: 10.1038/nrm.2015.3. Epub 2015 Nov 18.
8
Reevaluating αE-catenin monomer and homodimer functions by characterizing E-cadherin/αE-catenin chimeras.通过表征E-钙黏蛋白/αE-连环蛋白嵌合体重新评估αE-连环蛋白单体和同二聚体的功能
J Cell Biol. 2015 Sep 28;210(7):1065-74. doi: 10.1083/jcb.201411080.
9
Molecular mechanism of adenomatous polyposis coli-induced blockade of base excision repair pathway in colorectal carcinogenesis.腺瘤性结肠息肉病蛋白在结直肠癌发生过程中诱导碱基切除修复途径阻断的分子机制。
Life Sci. 2015 Oct 15;139:145-52. doi: 10.1016/j.lfs.2015.08.019. Epub 2015 Sep 1.
10
DNA damage induces nuclear actin filament assembly by Formin -2 and Spire-½ that promotes efficient DNA repair. [corrected].DNA损伤通过Formin-2和Spire-½诱导核肌动蛋白丝组装,从而促进高效的DNA修复。[已修正]
Elife. 2015 Aug 19;4:e07735. doi: 10.7554/eLife.07735.

细胞核α-连环蛋白通过β-连环蛋白和细胞核肌动蛋白介导DNA损伤反应。

Nuclear α-catenin mediates the DNA damage response via β-catenin and nuclear actin.

作者信息

Serebryannyy Leonid A, Yemelyanov Alex, Gottardi Cara J, de Lanerolle Primal

机构信息

Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL 60612, USA

Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

出版信息

J Cell Sci. 2017 May 15;130(10):1717-1729. doi: 10.1242/jcs.199893. Epub 2017 Mar 27.

DOI:10.1242/jcs.199893
PMID:28348105
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5450192/
Abstract

α-Catenin is an F-actin-binding protein widely recognized for its role in cell-cell adhesion. However, a growing body of literature indicates that α-catenin is also a nuclear protein. In this study, we show that α-catenin is able to modulate the sensitivity of cells to DNA damage and toxicity. Furthermore, nuclear α-catenin is actively recruited to sites of DNA damage. This recruitment occurs in a β-catenin-dependent manner and requires nuclear actin polymerization. These findings provide mechanistic insight into the WNT-mediated regulation of the DNA damage response and suggest a novel role for the α-catenin-β-catenin complex in the nucleus.

摘要

α-连环蛋白是一种F-肌动蛋白结合蛋白,因其在细胞间黏附中的作用而广为人知。然而,越来越多的文献表明,α-连环蛋白也是一种核蛋白。在本研究中,我们表明α-连环蛋白能够调节细胞对DNA损伤和毒性的敏感性。此外,核α-连环蛋白会被主动招募到DNA损伤位点。这种招募以β-连环蛋白依赖的方式发生,并且需要核肌动蛋白聚合。这些发现为WNT介导的DNA损伤反应调节提供了机制性见解,并提示了α-连环蛋白-β-连环蛋白复合物在细胞核中的新作用。