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一种Smad转录共抑制因子。

A Smad transcriptional corepressor.

作者信息

Wotton D, Lo R S, Lee S, Massagué J

机构信息

Cell Biology Program, Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

Cell. 1999 Apr 2;97(1):29-39. doi: 10.1016/s0092-8674(00)80712-6.

Abstract

Following TGFbeta receptor-mediated phosphorylation and association with Smad4, Smad2 moves into the nucleus, binds to target promoters in association with DNA-binding cofactors, and recruits coactivators such as p300/CBP to activate transcription. We identified the homeodomain protein TGIF as a Smad2-binding protein and a repressor of transcription. A TGFbeta-activated Smad complex can recruit TGIF and histone deacetylases (HDACs) to a Smad target promoter, repressing transcription. Thus, upon entering the nucleus, a Smad2-Smad4 complex may interact with coactivators, forming a transcriptional activation complex, or with TGIF and HDACs, forming a transcriptional repressor complex. Formation of one of these two mutually exclusive complexes is determined by the relative levels of Smad corepressors and coactivators within the cell.

摘要

在转化生长因子β(TGFβ)受体介导的磷酸化并与Smad4结合后,Smad2进入细胞核,与DNA结合辅助因子一起结合到靶启动子上,并募集共激活因子如p300/CBP来激活转录。我们鉴定出同源结构域蛋白TGIF是一种Smad2结合蛋白和转录抑制因子。TGFβ激活的Smad复合物可将TGIF和组蛋白脱乙酰基酶(HDACs)募集到Smad靶启动子上,从而抑制转录。因此,进入细胞核后,Smad2-Smad4复合物可能与共激活因子相互作用,形成转录激活复合物,或者与TGIF和HDACs相互作用,形成转录抑制复合物。这两种互斥复合物之一的形成取决于细胞内Smad共抑制因子和共激活因子的相对水平。

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