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DNA甲基化偶联转录抑制的动态调控:MeCP2对脑源性神经营养因子的调控

Dynamic regulation of DNA methylation coupled transcriptional repression: BDNF regulation by MeCP2.

作者信息

Wade Paul A

机构信息

Emory University, Department of Pathology and Laboratory Medicine, Whitehead Research Building Room 142, 615 Michael Street, Atlanta, GA 30322, USA.

出版信息

Bioessays. 2004 Mar;26(3):217-20. doi: 10.1002/bies.20018.

Abstract

A recurrent theme in eukaryotic genome regulation stipulates that the properties of DNA are strongly influenced by the nucleoprotein complex into which it is assembled. Methylation of cytosine residues in vertebrate genomes has been implicated in influencing the assembly of locally repressive chromatin architecture. Current models suggest that covalent modification of DNA results in heritable, long-term transcriptional silencing. In October of 2003, two manuscripts were published that challenge important aspects of this model, suggesting that modulation of both DNA methylation itself, as well as the machinery implicated in its interpretation, are involved in acute gene regulation.

摘要

真核生物基因组调控中的一个反复出现的主题表明,DNA的特性受到其组装而成的核蛋白复合体的强烈影响。脊椎动物基因组中胞嘧啶残基的甲基化与局部抑制性染色质结构的组装有关。目前的模型表明,DNA的共价修饰会导致可遗传的长期转录沉默。2003年10月,两篇论文发表,对该模型的重要方面提出了挑战,表明DNA甲基化本身以及参与其解读的机制的调节都参与了急性基因调控。

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