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哺乳动物转录抑制因子RBP(CBF1)靶向TFIID和TFIIA以阻止激活转录。

The mammalian transcriptional repressor RBP (CBF1) targets TFIID and TFIIA to prevent activated transcription.

作者信息

Olave I, Reinberg D, Vales L D

机构信息

Department of Biochemistry, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854 USA.

出版信息

Genes Dev. 1998 Jun 1;12(11):1621-37. doi: 10.1101/gad.12.11.1621.

Abstract

RBP is a cellular protein that functions as a transcriptional repressor in mammalian cells. RBP has elicited great interest lately because of its established roles in regulating gene expression, in Drosophila and mouse development, and as a component of the Notch signal transduction pathway. This report focuses on the mechanism by which RBP represses transcription and thereby regulates expression of a relatively simple, but natural, promoter. The results show that, irrespective of the close proximity between RBP and other transcription factors bound to the promoter, RBP does not occlude binding by these other transcription factors. Instead, RBP interacts with two transcriptional coactivators: dTAFII110, a subunit of TFIID, and TFIIA to repress transcription. The domain of dTAFII110 targeted by RBP is the same domain that interacts with TFIIA, but is disparate from the domain that interacts with Sp1. Repression can be thwarted when stable transcription preinitiation complexes are formed before RBP addition, suggesting that RBP interaction with TFIIA and TFIID perturbs optimal interactions between these coactivators. Consistent with this, interaction between RBP and TFIIA precludes interaction with dTAFII110. This is the first report of a repressor specifically targeting these two coactivators to subvert activated transcription.

摘要

RBP是一种细胞蛋白,在哺乳动物细胞中作为转录抑制因子发挥作用。由于RBP在调节基因表达、果蝇和小鼠发育以及作为Notch信号转导途径的一个组成部分方面已确立的作用,它最近引起了极大的关注。本报告重点关注RBP抑制转录从而调节一个相对简单但天然的启动子表达的机制。结果表明,无论RBP与结合在启动子上的其他转录因子之间的距离有多近,RBP都不会阻碍这些其他转录因子的结合。相反,RBP与两种转录共激活因子相互作用:TFIID的一个亚基dTAFII110和TFIIA,以抑制转录。RBP靶向的dTAFII110结构域与与TFIIA相互作用的结构域相同,但与与Sp1相互作用的结构域不同。当在添加RBP之前形成稳定的转录起始前复合物时,抑制作用可能会受到阻碍,这表明RBP与TFIIA和TFIID的相互作用扰乱了这些共激活因子之间的最佳相互作用。与此一致的是,RBP与TFIIA之间的相互作用排除了与dTAFII110的相互作用。这是关于一种阻遏物特异性靶向这两种共激活因子以颠覆激活转录的首次报道。

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