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染色质修饰:衰老和老化的驱动力?

Chromatin modifications: the driving force of senescence and aging?

作者信息

Dimauro Teresa, David Gregory

机构信息

Department of Pharmacology, NYU Langone Medical Center, New York, NY 10016, USA.

出版信息

Aging (Albany NY). 2009 Feb 13;1(2):182-90. doi: 10.18632/aging.100023.

DOI:10.18632/aging.100023
PMID:20157508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2806002/
Abstract

An emerging field of investigation in the search for treatment of human disease is the modulation of chromatin modifications. Chromatin modifications impart virtually all processes occurring in the mammalian nucleus, from regulation of transcription to genomic stability and nuclear high order organization. It has been well recognized that, as the mammalian cell ages, its chromatin structure evolves, both at a global level and at specific loci. While these observations are mostly correlative, recent technical developments allowing loss-of-function experiments and genome-wide approaches have permitted the identification of a causal relationship between specific changes in chromatin structure and the aging phenotype. Here we review the evidence pointing to the modulation of chromatin structure as a potential driving force of cellular aging in mammals.

摘要

在寻找人类疾病治疗方法的过程中,一个新兴的研究领域是染色质修饰的调控。染色质修饰几乎影响着哺乳动物细胞核内发生的所有过程,从转录调控到基因组稳定性和核高级结构组织。人们已经充分认识到,随着哺乳动物细胞的衰老,其染色质结构在整体水平和特定基因座都会发生变化。虽然这些观察大多只是相关性的,但最近允许进行功能丧失实验和全基因组方法的技术发展,使得人们能够确定染色质结构的特定变化与衰老表型之间的因果关系。在这里,我们综述了表明染色质结构调控是哺乳动物细胞衰老潜在驱动力的证据。

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本文引用的文献

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SIRT6 stabilizes DNA-dependent protein kinase at chromatin for DNA double-strand break repair.SIRT6使染色质上的DNA依赖性蛋白激酶稳定,以进行DNA双链断裂修复。
Aging (Albany NY). 2009 Jan 15;1(1):109-21. doi: 10.18632/aging.100011.
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dSir2 and Dmp53 interact to mediate aspects of CR-dependent lifespan extension in D. melanogaster.Sir2和Dmp53相互作用,介导黑腹果蝇中与CR相关的寿命延长的各个方面。
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The A- and B-type nuclear lamin networks: microdomains involved in chromatin organization and transcription.A 型和 B 型核纤层网络:参与染色质组织和转录的微结构域。
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SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging.SIRT1在染色质上的重新分布促进基因组稳定性,但在衰老过程中会改变基因表达。
Cell. 2008 Nov 28;135(5):907-18. doi: 10.1016/j.cell.2008.10.025.
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The H3K36 demethylase Jhdm1b/Kdm2b regulates cell proliferation and senescence through p15(Ink4b).H3K36去甲基化酶Jhdm1b/Kdm2b通过p15(Ink4b)调节细胞增殖和衰老。
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Re-positioning genes to the nuclear envelope in mammalian cells: impact on transcription.将基因重新定位到哺乳动物细胞的核膜:对转录的影响。
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Genes Dev. 2008 Aug 1;22(15):2048-61. doi: 10.1101/gad.476008.
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Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease.擦除甲基标记:处于细胞分化和疾病核心的组蛋白去甲基化酶
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