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Repression of Smad transcriptional activity by PIASy, an inhibitor of activated STAT

机译:PIASy(活化的STAT的抑制剂)抑制Smad转录活性

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Smad proteins mediate transforming growth factor beta (TGF-beta)-inducible transcriptional responses. Protein inhibitor of activated signal transducer and activator of transcription (PIAS) represents a family of proteins that inhibits signal transducer and activator of transcription and also regulates other transcriptional responses. In an effort to identify Smad-interacting proteins by a yeast three-hybrid screen with Smad3 and Smad4 as baits, we identified PIASy, a member of the PIAS family. In yeast, PIASy interacts strongly with Smad4 and also with receptor-regulated Smads. In mammalian cells, PIASy binds most strongly with Smad3 and also associates with other receptor-regulated Smads and Smad4. The interaction between Smad3 and PIASy is increased in the presence of TGF-beta and occurs through the C-terminal domain of Smad3. Moreover, Smad3, Smad4, and PIASy can form a ternary complex. PIASy does not inhibit Smad complex binding to DNA, but it represses Smad transcriptional activity. Interestingly, conditional overexpression of PIASy selectively inhibits a subset of endogenous TGF-beta-responsive genes, which includes the cyclin-dependent kinase inhibitor p15, and the plasminogen activator inhibitor 1. We further show that PIASy can interact constitutively with histone deacetylase 1 (HDAC1) and that addition of HDAC inhibitor trichostatin A (TSA) can prevent the inhibitory function of PIASy. Taken together, our studies indicate that PIASy can inhibit TGF-beta/Smad transcriptional responses through interactions with Smad proteins and HDAC. [References: 55]
机译:Smad蛋白介导转化生长因子β(TGF-β)诱导的转录反应。激活的信号转导子和转录激活子(PIAS)的蛋白抑制剂代表一系列蛋白,它们抑制信号的转导子和转录激活子并调节其他转录反应。为了通过以Smad3和Smad4为诱饵的酵母三杂交筛选识别Smad相互作用蛋白,我们鉴定了PIASy家族的成员PIASy。在酵母中,PIASy与Smad4以及与受体调节的Smads强烈相互作用。在哺乳动物细胞中,PIASy与Smad3的结合最牢固,并且还与其他受体调节的Smads和Smad4结合。在存在TGF-β的情况下,Smad3与PIASy之间的相互作用会增强,并通过Smad3的C端结构域发生。此外,Smad3,Smad4和PIASy可以形成三元复合物。 PIASy不会抑制Smad复合物与DNA的结合,但会抑制Smad的转录活性。有趣的是,PIASy的条件性过表达选择性抑制了内源性TGF-β反应基因的子集,其中包括细胞周期蛋白依赖性激酶抑制剂p15和纤溶酶原激活物抑制剂1。我们进一步证明PIASy可以与组蛋白脱乙酰基酶1(HDAC1 ),并且加入HDAC抑制剂曲古抑菌素A(TSA)可以阻止PIASy的抑制功能。两者合计,我们的研究表明PIASy可以通过与Smad蛋白和HDAC相互作用来抑制TGF-beta / Smad转录反应。 [参考:55]

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