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SNAPc: a core promoter factor with a built-in DNA-binding damper that is deactivated by the Oct-1 POU domain

机译:SNAPc:具有内置DNA结合阻尼器的核心启动子因子可被Oct-1 POU域失活

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摘要

snRNA gene transcription is activated in part by recruitment of SNAPc to the core promoter through protein–protein contacts with the POU domain of the enhancer-binding factor Oct-1. We show that a mini-SNAPc consisting of a subset of SNAPc subunits is capable of directing both RNA polymerase II (Pol II) and Pol III snRNA gene transcription. Mini-SNAPc cannot be recruited by Oct-1, but binds as efficiently to the promoter as SNAPc together with Oct-1 and directs activated RNA Pol III transcription. Thus, SNAPc represses its own binding to DNA, and repression is relieved by interactions with the Oct-1 POU domain that promote cooperative binding. We have shown previously that TBP also represses its own binding, and in that case repression is relieved by cooperative interactions with SNAPc. This may represent a general mechanism to ensure that core promoter-binding factors, which have strikingly slow off-rates, are recruited specifically to promoter sequences rather than to cryptic-binding sites in the genome.
机译:通过与增强子结合因子Oct-1的POU结构域的蛋白质接触将SNAPc募集到核心启动子,部分激活了snRNA基因转录。我们显示迷你SNAPc的SNAPc亚基的一个子集是能够指导RNA聚合酶II(Pol II)和Pol III snRNA基因转录。 Mini-SNAPc不能被Oct-1募集,但是与OctAP一样有效地与SNAPc结合到启动子上,并指导活化的RNA Pol III转录。因此,SNAPc抑制其自身与DNA的结合,并通过与促进协同结合的Oct-1 POU域相互作用来缓解抑制。先前我们已经表明,TBP还抑制其自身的绑定,在这种情况下,通过与SNAPc的协作交互来缓解抑制。这可能代表了确保核心启动子结合因子(具有显着减慢速率)被专门募集到启动子序列而不是基因组中的隐秘结合位点的一般机制。

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