首页> 外文期刊>The Biochemical Journal >Transcriptional autorepression of Msx1 gene is mediated by interactions of Msx1 protein with a multi-protein transcriptional complex containing TATA-binding protein, Sp1 and cAMP-response-element-binding protein-binding protein (CBP/p300).
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Transcriptional autorepression of Msx1 gene is mediated by interactions of Msx1 protein with a multi-protein transcriptional complex containing TATA-binding protein, Sp1 and cAMP-response-element-binding protein-binding protein (CBP/p300).

机译:Msx1基因的转录自动阻遏是通过Msx1蛋白与包含TATA结合蛋白,Sp1和cAMP-反应-元素-结合蛋白结合蛋白(CBP / p300)的多蛋白转录复合物相互作用而介导的。

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摘要

The TATA-less murine Msx1 promoter contains two Msx1-binding motifs, located at -568 to -573 and +25 to +30, and is subject to potent autorepression [Takahashi, Guron, Shetty, Matsui and Raghow (1997) J. Biol. Chem. 272, 22667-22678]. To investigate the molecular mechanism by which Msx1 represses the activity of its own promoter, we transfected C2C12 myoblasts with Msx1-promoter-luciferase constructs and assessed reporter gene activity, with and without the exogenous expression of Msx1. We demonstrate that Msx1-mediated autorepression remained unaffected, regardless of the presence or absence of the Msx1 recognition motifs on the promoter. Furthermore, graded exogenous expression of TATA-binding protein (TBP), Sp1 or cAMP-response-element-binding protein-binding protein (CBP/p300) could counteract the autoinhibitory activity of Msx1. Finally, we demonstrate that Msx1 protein can be immunoprecipitated in a multiprotein complex containing TBP, Sp1 and CBP/p300. We hypothesize that the interaction of Msx1 protein with one or more ubiquitous or tissue-restricted transcription factors mediates transcriptional autorepression of the Msx1 gene.
机译:不含TATA的鼠Msx1启动子包含两个Msx1结合基序,位于-568至-573和+25至+30,并受到有效的自抑制作用[Takahashi,Guron,Shetty,Matsui和Raghow(1997)J. Biol 。化学272,22667-22678]。要研究Msx1抑制其自身启动子活性的分子机制,我们用Msx1启动子荧光素酶构建体转染了C2C12成肌细胞,并评估了有无Msx1外源表达的报道基因活性。我们证明,无论启动子上是否存在Msx1识别基元,Msx1介导的自动阻遏作用均不受影响。此外,TATA结合蛋白(TBP),Sp1或cAMP反应元件结合蛋白结合蛋白(CBP / p300)的分级外源表达可以抵消Msx1的自抑制活性。最后,我们证明Msx1蛋白可以在包含TBP,Sp1和CBP / p300的多蛋白复合物中被免疫沉淀。我们假设Msx1蛋白与一个或多个普遍存在或组织受限的转录因子的相互作用介导了Msx1基因的转录自抑制。

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