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核小体重塑去乙酰化酶复合物:连接组蛋白修饰与核小体重塑

The NuRD complex: linking histone modification to nucleosome remodeling.

作者信息

Feng Q, Zhang Y

机构信息

Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, NC 27599-7295, USA.

出版信息

Curr Top Microbiol Immunol. 2003;274:269-90. doi: 10.1007/978-3-642-55747-7_10.

Abstract

ATP-dependent nucleosome remodeling and core histone tail modifications play important roles in chromatin function. Purification and characterization of the NuRD/Mi-2 complex, which possesses both nucleosome remodeling and histone deacetylase activities, suggests that ATP-dependent nucleosome remodeling and histone tail modification can be coupled. Recent studies indicate that NuRD is an integral part of the MeCP1 complex, suggesting that nucleosome remodeling and histone deacetylation play important roles in methylated DNA silencing. Studies in Caenorhabditis elegans have revealed important functions of the NuRD complex in embryonic patterning and Ras signaling. Accumulating evidence indicates that NuRD may regulate transcription of specific genes by interacting with specific transcriptional factors. In addition, it may also participate in genome-wide transcriptional regulation through an association with histone tails.

摘要

ATP 依赖的核小体重塑和核心组蛋白尾部修饰在染色质功能中发挥重要作用。具有核小体重塑和组蛋白去乙酰化酶活性的 NuRD/Mi-2 复合物的纯化与特性分析表明,ATP 依赖的核小体重塑和组蛋白尾部修饰可能相互关联。最近的研究表明,NuRD 是 MeCP1 复合物的一个组成部分,这表明核小体重塑和组蛋白去乙酰化在甲基化 DNA 沉默中起重要作用。秀丽隐杆线虫的研究揭示了 NuRD 复合物在胚胎模式形成和 Ras 信号传导中的重要功能。越来越多的证据表明,NuRD 可能通过与特定转录因子相互作用来调节特定基因的转录。此外,它还可能通过与组蛋白尾部结合参与全基因组转录调控。

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