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腺病毒E1A对YY1转录抑制的解除是由E1A相关蛋白p300介导的。

Relief of YY1 transcriptional repression by adenovirus E1A is mediated by E1A-associated protein p300.

作者信息

Lee J S, Galvin K M, See R H, Eckner R, Livingston D, Moran E, Shi Y

机构信息

Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Genes Dev. 1995 May 15;9(10):1188-98. doi: 10.1101/gad.9.10.1188.

Abstract

YY1 represses transcription when bound upstream of transcriptional initiation sites. This repression can be relieved by adenovirus E1A. Here, we present genetic evidence that the ability of E1A to relieve YY1 repression was impaired by mutations that affect E1A binding to its associated protein p300. This suggests that E1A may modulate the repressor activity of YY1 by binding to p300, which may be physically complexed with YY1. A YY1/p300 protein complex in vivo was demonstrated by several independent approaches, and the YY1-interacting domain was mapped to the carboxy-terminal region of p300, distinct from the E1A-binding site. Unlike E2F/RB, the YY1/p300 complex is not disrupted by E1A. Functional studies using recombinant p300 demonstrated unequivocally that p300 is capable of mediating E1A-induced transcriptional activation through YY1. Taken together, these results reveal, for the first time, a YY1/p300 complex that is targeted by E1A and demonstrate a function for p300 in mediating interactions between YY1 and E1A. Our data thus identify YY1 as a partner protein for p300 and uncover a molecular mechanism for the relief of YY1-mediated repression by E1A.

摘要

当YY1结合在转录起始位点上游时,它会抑制转录。腺病毒E1A可以解除这种抑制作用。在此,我们提供了遗传学证据,表明影响E1A与其相关蛋白p300结合的突变会损害E1A解除YY1抑制的能力。这表明E1A可能通过与p300结合来调节YY1的阻遏活性,而p300可能与YY1形成物理复合物。通过几种独立的方法在体内证实了YY1/p300蛋白复合物的存在,并且将与YY1相互作用的结构域定位到p300的羧基末端区域,该区域与E1A结合位点不同。与E2F/RB不同,YY1/p300复合物不会被E1A破坏。使用重组p300进行的功能研究明确表明,p300能够通过YY1介导E1A诱导的转录激活。综上所述,这些结果首次揭示了一种被E1A靶向的YY1/p300复合物,并证明了p300在介导YY1和E1A之间相互作用中的功能。因此,我们的数据将YY1鉴定为p300的伴侣蛋白,并揭示了E1A解除YY1介导的抑制作用的分子机制。

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