哺乳动物端粒处的染色质调控和非编码 RNA

Chromatin regulation and non-coding RNAs at mammalian telomeres.

机构信息

Telomeres and Telomerase Group, Molecular Oncology Program, Spanish National Cancer Research Centre (CNIO), Melchor Fernandez Almagro 3, 28029 Madrid, Spain.

出版信息

Semin Cell Dev Biol. 2010 Apr;21(2):186-93. doi: 10.1016/j.semcdb.2009.09.015. Epub 2009 Oct 6.

Abstract

In eukaryotes, terminal chromosome repeats are bound by a specialized nucleoprotein complex that controls telomere length and protects chromosome ends from DNA repair and degradation. In mammals the "shelterin" complex mediates these central functions at telomeres. In the recent years it has become evident that also the heterochromatic structure of mammalian telomeres is implicated in telomere length regulation. Impaired telomeric chromatin compaction results in a loss of telomere length control. Progressive telomere shortening affects chromatin compaction at telomeric and subtelomeric repeats and activates alternative telomere maintenance mechanisms. Dynamics of chromatin structure of telomeres during early mammalian development and nuclear reprogramming further indicates a central role of telomeric heterochromatin in organismal development. In addition, the recent discovery that telomeres are transcribed, giving rise to UUAGGG-repeat containing TelRNAs/TERRA, opens a new level of chromatin regulation at telomeres. Understanding the links between the epigenetic status of telomeres, TERRA/TelRNA and telomere homeostasis will open new avenues for our understanding of organismal development, cancer and ageing.

摘要

在真核生物中,端粒重复序列被一种特殊的核蛋白复合物所结合,这种复合物控制着端粒的长度,并保护染色体末端免受 DNA 修复和降解的影响。在哺乳动物中,“庇护素”复合物在端粒处介导这些核心功能。近年来,人们已经清楚地认识到,哺乳动物端粒的异染色质结构也参与了端粒长度的调节。端粒染色质的压缩受损会导致端粒长度失去控制。端粒逐渐缩短会影响端粒和着丝粒重复序列的染色质压缩,并激活替代的端粒维持机制。在早期哺乳动物发育和核重编程过程中端粒染色质结构的动力学进一步表明,端粒异染色质在机体发育中起着核心作用。此外,最近发现端粒是转录的,产生含有 UUAGGG 重复的 TelRNAs/TERRA,这为端粒的染色质调控开辟了一个新的层次。了解端粒的表观遗传状态、TERRA/TelRNA 和端粒稳态之间的联系,将为我们理解机体发育、癌症和衰老开辟新的途径。

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