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首页> 外文期刊>Molecular and Cellular Biology >Positive and Negative Regulation of the Cardiovascular Transcription Factor KLF5 by p300 and the Oncogenic Regulator SET through Interaction and Acetylation on the DNA-Binding Domain
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Positive and Negative Regulation of the Cardiovascular Transcription Factor KLF5 by p300 and the Oncogenic Regulator SET through Interaction and Acetylation on the DNA-Binding Domain

机译:p300对心血管转录因子KLF5的正负调节作用以及通过DNA结合域上的相互作用和乙酰化作用调节致癌调节剂SET

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Here we show a novel pathway of transcriptional regulation of a DNA-binding transcription factor by coupled interaction and modification (e.g., acetylation) through the DNA-binding domain (DBD). The oncogenic regulator SET was isolated by affinity purification of factors interacting with the DBD of the cardiovascular transcription factor KLF5. SET negatively regulated KLF5 DNA binding, transactivation, and cell-proliferative activities. Down-regulation of the negative regulator SET was seen in response to KLF5-mediated gene activation. The coactivator/acetylase p300, on the other hand, interacted with and acetylated KLF5 DBD, and activated its transcription. Interestingly, SET inhibited KLF5 acetylation, and a nonacetylated mutant of KLF5 showed reduced transcriptional activation and cell growth complementary to the actions of SET. These findings suggest a new pathway for regulation of a DNA-binding transcription factor on the DBD through interaction and coupled acetylation by two opposing regulatory factors of a coactivator/acetylase and a negative cofactor harboring activity to inhibit acetylation.
机译:在这里,我们显示了通过结合相互作用和修饰(例如,乙酰化)通过DNA结合域(DBD)的DNA结合转录因子的转录调节的新途径。通过亲和纯化与心血管转录因子KLF5的DBD相互作用的因子,分离出致癌调节剂SET。 SET负调节KLF5 DNA的结合,反式激活和细胞增殖活性。看到负调节剂SET的下调是对KLF5介导的基因激活的响应。另一方面,辅助激活剂/乙酰化酶p300与KLF5 DBD相互作用并被其乙酰化,从而激活其转录。有趣的是,SET抑制了KLF5的乙酰化作用,而KLF5的非乙酰化突变体显示出与SET的作用互补的转录激活和细胞生长降低。这些发现提示了通过相互作用和偶联乙酰化作用来调节DBD上的DNA结合转录因子的新途径,该作用是通过两个相对的调节因子/辅酶/乙酰化酶和负的辅因子具有抑制乙酰化作用的。

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