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靶基因背景影响 KAT3 家族的 CBP 和 p300 组蛋白乙酰转移酶的转录需求。

Target gene context influences the transcriptional requirement for the KAT3 family of CBP and p300 histone acetyltransferases.

机构信息

Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, TN, USA.

出版信息

Epigenetics. 2010 Jan 1;5(1):9-15. doi: 10.4161/epi.5.1.10449. Epub 2010 Jan 27.

Abstract

One general principle of gene regulation is that DNA-binding transcription factors modulate transcription by recruiting cofactors that modify histones and chromatin structure. A second implicit principle is that a particular cofactor is necessary at all the target genes where the cofactor is recruited. Increasingly, these principles do not appear to be absolute, as experimentally defined relationships between transcription, cofactors and chromatin modification grow in complexity. The KAT3 histone acetyltransferases CREB binding protein (CBP) and p300 have at least 400 interacting protein partners, thereby acting as hubs in gene regulatory networks. Studies using mutant primary cells indicate that the occurrence of CBP and p300 at any given target gene sometimes correlates with, rather than dictates transcription. This suggests that there are unexpected levels of redundancy between CBP/p300 and other unrelated coactivators, or that CBP/p300 recruitment may sometimes be coincidental. A transcription factor may therefore recruit the same group of coactivators as part of its "toolbox", but it is the characteristics of the individual target gene that determine which coactivation "tools" are required for its transcription.

摘要

基因调控的一个普遍原则是,DNA 结合转录因子通过招募改变组蛋白和染色质结构的辅助因子来调节转录。第二个隐含的原则是,特定的辅助因子在被招募的所有靶基因中都是必需的。越来越多的证据表明,这些原则似乎并不绝对,因为转录、辅助因子和染色质修饰之间的实验定义关系变得越来越复杂。KAT3 组蛋白乙酰转移酶 CREB 结合蛋白 (CBP) 和 p300 至少有 400 个相互作用的蛋白伴侣,因此它们作为基因调控网络的枢纽。使用突变原代细胞的研究表明,CBP 和 p300 在任何给定的靶基因上的出现有时与转录相关,而不是决定转录。这表明 CBP/p300 和其他不相关的共激活因子之间存在意想不到的冗余水平,或者 CBP/p300 的募集有时可能是偶然的。因此,转录因子可能会将相同的一组共激活因子作为其“工具箱”的一部分进行招募,但决定其转录所需的共激活“工具”的是单个靶基因的特征。

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