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融合还是不融合:检查点和 DNA 修复蛋白如何维持端粒?

To fuse or not to fuse: how do checkpoint and DNA repair proteins maintain telomeres?

机构信息

Department of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL 60607, USA.

出版信息

Front Biosci (Landmark Ed). 2010 Jun 1;15(3):1105-18. doi: 10.2741/3664.

Abstract

DNA damage checkpoint and DNA repair mechanisms play critical roles in the stable maintenance of genetic information. Various forms of DNA damage that arise inside cells due to common errors in normal cellular processes, such as DNA replication, or due to exposure to various DNA damaging agents, must be quickly detected and repaired by checkpoint signaling and repair factors. Telomeres, the natural ends of linear chromosomes, share many features with undesired "broken" DNA, and are recognized and processed by various DNA damage checkpoint and DNA repair proteins. However, their modes of action at telomeres must be altered from their actions at other DNA damage sites to avoid telomere fusions and permanent cell cycle arrest. Interestingly, accumulating evidence indicates that DNA damage checkpoint and DNA repair proteins are essential for telomere maintenance. In this article, we review our current knowledge on various mechanisms by which DNA damage checkpoint and DNA repair proteins are modulated at telomeres and how they might contribute to telomere maintenance in eukaryotes.

摘要

DNA 损伤检查点和 DNA 修复机制在稳定维持遗传信息方面发挥着关键作用。由于正常细胞过程中的常见错误(如 DNA 复制)或由于暴露于各种 DNA 损伤剂,细胞内会产生各种形式的 DNA 损伤,必须通过检查点信号和修复因子快速检测和修复。端粒是线性染色体的自然末端,与不想要的“断裂”DNA 具有许多共同特征,并且被各种 DNA 损伤检查点和 DNA 修复蛋白识别和处理。然而,它们在端粒上的作用方式必须与其在其他 DNA 损伤部位的作用方式不同,以避免端粒融合和永久性细胞周期停滞。有趣的是,越来越多的证据表明,DNA 损伤检查点和 DNA 修复蛋白对于端粒维持是必不可少的。在本文中,我们回顾了目前关于 DNA 损伤检查点和 DNA 修复蛋白在端粒上的各种调节机制的知识,以及它们如何有助于真核生物的端粒维持。

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本文引用的文献

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