首页> 美国卫生研究院文献>Nucleic Acids Research >CpG methylation has differential effects on the binding of YY1 and ETS proteins to the bi-directional promoter of the Surf-1 and Surf-2 genes.
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CpG methylation has differential effects on the binding of YY1 and ETS proteins to the bi-directional promoter of the Surf-1 and Surf-2 genes.

机译:CpG甲基化对YY1和ETS蛋白与Surf-1和Surf-2基因的双向启动子的结合具有不同的影响。

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摘要

The divergently transcribed Surf-1 and Surf-2 housekeeping genes are separated by a bi-directional, TATA-less promoter which lies within a CpG-rich island. Here we show that CpG methylation severely reduces transcription in the direction of both Surf-1 and Surf-2. Previous work has identified three promoter elements (Su1, Su2 and Su3) which are conserved between the human and mouse Surf-1/Surf-2 promoters. These elements bind transcription factors present in human and mouse cell nuclear extracts in vitro and mutations which prevent factor binding also reduce promoter activity in vivo. Transcription initiation factor YY1 binds to the Su1 site and stimulates transcription in the direction of Surf-1 and, to a lesser extent, Surf-2. Here we show that members of the ETS family of transcription factors bind to the Su2 site. Although the Su1 factor binding site contains three CpG dinucleotides, the binding of YY1 is not affected by CpG methylation. In contrast, CpG methylation abolishes the binding of ETS proteins to the Su2 site; methylation of a single cytosine, at position 3 of the consensus ETS site, is sufficient to prevent factor binding. This direct effect on the binding of ETS proteins is, however, not in itself sufficient to explain the repression of this promoter by CpG methylation. A mutation of the Su2 site which removes the sequence CpG, but which does not prevent ETS factor binding, fails to relieve this promoter from repression by CpG methylation.
机译:转录不同的Surf-1和Surf-2看家基因被位于CpG丰富的岛内的双向,无TATA的启动子隔开。在这里,我们显示CpG甲基化严重降低了Surf-1和Surf-2方向的转录。先前的工作已经确定了三个启动子元件(Su1,Su2和Su3),它们在人类和小鼠Surf-1 / Surf-2启动子之间是保守的。这些元件结合体外存在于人和小鼠细胞核提取物中的转录因子,并且阻止因子结合的突变也降低了体内启动子的活性。转录起始因子YY1与Su1位点结合,并在Surf-1方向(较小程度上,在Surf-2方向)上刺激转录。在这里,我们显示ETS转录因子家族的成员与Su2位点结合。尽管Su1因子结合位点包含三个CpG二核苷酸,但YY1的结合不受CpG甲基化的影响。相反,CpG甲基化消除了ETS蛋白与Su2位点的结合。在共有ETS位点的3位上,单个胞嘧啶的甲基化足以防止因子结合。然而,对ETS蛋白结合的直接影响本身不足以解释CpG甲基化对该启动子的抑制作用。 Su2位点的突变可除去序列CpG,但不能阻止ETS因子结合,不能使该启动子免受CpG甲基化的抑制。

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