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端粒:保护染色体免受基因组不稳定的影响。

Telomeres: protecting chromosomes against genome instability.

机构信息

The Salk Institute for Biological Studies, Molecular and Cell Biology Laboratory, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Nat Rev Mol Cell Biol. 2010 Mar;11(3):171-81. doi: 10.1038/nrm2848. Epub 2010 Feb 3.


DOI:10.1038/nrm2848
PMID:20125188
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2842081/
Abstract

The natural ends of linear chromosomes require unique genetic and structural adaptations to facilitate the protection of genetic material. This is achieved by the sequestration of the telomeric sequence into a protective nucleoprotein cap that masks the ends from constitutive exposure to the DNA damage response machinery. When telomeres are unmasked, genome instability arises. Balancing capping requirements with telomere replication and the enzymatic processing steps that are obligatory for telomere function is a complex problem. Telomeric proteins and their interacting factors create an environment at chromosome ends that inhibits DNA repair; however, the repair machinery is essential for proper telomere function.

摘要

线性染色体的自然末端需要独特的遗传和结构适应,以促进遗传物质的保护。这是通过将端粒序列隔离到保护性核蛋白帽中来实现的,该帽可防止末端固有地暴露于 DNA 损伤反应机制。当端粒被揭开时,就会出现基因组不稳定。端粒复制和酶处理步骤与端粒功能的必需性之间的平衡是一个复杂的问题。端粒蛋白及其相互作用因子在染色体末端创造了一种抑制 DNA 修复的环境;然而,修复机制对于端粒功能的正常发挥是必不可少的。

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本文引用的文献

[1]
Human DNA methylomes at base resolution show widespread epigenomic differences.

Nature. 2009-11-19

[2]
Chromatin regulation and non-coding RNAs at mammalian telomeres.

Semin Cell Dev Biol. 2009-10-6

[3]
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EMBO J. 2009-11-4

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Mol Cell. 2009-8-28

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Genes Dev. 2009-9-1

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Mol Cell Biol. 2009-10

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Cell. 2009-8-7

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Multiple roles for MRE11 at uncapped telomeres.

Nature. 2009-8-13

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TERRA: telomeric repeat-containing RNA.

EMBO J. 2009-9-2

[10]
A two-step model for senescence triggered by a single critically short telomere.

Nat Cell Biol. 2009-8

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