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High-Level Activation of Transcription of the Yeast U6 snRNA Gene in Chromatin by the Basal RNA Polymerase III Transcription Factor TFIIIC

机译:基底RNA聚合酶III转录因子TFIIIC对染色质中酵母U6 snRNA基因的转录的高水平激活

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摘要

Transcription of the U6 snRNA gene (SNR6) in Saccharomyces cerevisiae by RNA polymerase III (pol III) requires TFIIIC and its box A and B binding sites. In contrast, TFIIIC has little or no effect on SNR6 transcription with purified components in vitro due to direct recognition of the SNR6 TATA box by TFIIIB. When SNR6 was assembled into chromatin in vitro by use of the Drosophila melanogaster S-190 extract, transcription of these templates with highly purified yeast pol III, TFIIIC, and TFIIIB displayed a near-absolute requirement for TFIIIC but yielded a 5- to 15-fold-higher level of transcription relative to naked DNA (>100-fold activation over repressed chromatin). Analysis of chromatin structure demonstrated that TFIIIC binding leads to remodeling of U6 gene chromatin, resulting in positioning of a nucleosome between boxes A and B. The resulting folding of the intervening DNA into the nucleosome could bring the suboptimally spaced SNR6 box A and B elements into greater proximity and thus facilitate activation of transcription. In the absence of ATP, however, the binding of TFIIIC to box B in chromatin was not accompanied by remodeling and the transcription activation was ∼35% of that seen in its presence, implying that both TFIIIC binding and ATP-dependent chromatin remodeling were required for the full activation of the gene. Our results suggest that TFIIIC, which is a basal transcription factor of pol III, also plays a direct role in remodeling chromatin on the SNR6 gene.
机译:RNA聚合酶III(pol III)在酿酒酵母中转录U6 snRNA基因(SNR6)需要TFIIIC及其框A和框B的结合位点。相反,由于TFIIIB直接识别SNR6 TATA框,因此TFIIIC在体外用纯化的成分对SNR6转录几乎没有影响。当使用果蝇S-190提取物将SNR6体外组装到染色质中时,用高度纯化的酵母pol III,TFIIIC和TFIIIB转录这些模板显示出对TFIIIC几乎绝对的要求,但产生了5至15-相对于裸露的DNA而言,转录水平提高了1倍(与抑制的染色质相比,活化程度提高了100倍)。染色质结构分析表明,TFIIIC结合导致U6基因染色质重塑,从而导致核小体位于A和B盒之间。插入的DNA折叠进入核小体中会导致亚最佳间隔的SNR6盒A和B元素进入更大的亲和力,从而促进转录激活。然而,在没有ATP的情况下,TFIIIC与染色质中框B的结合并不伴随重塑,转录激活程度约为存在时的35%,这意味着既需要TFIIIC结合又需要依赖ATP的染色质重塑完全激活基因。我们的结果表明,TFIIIC是pol III的基础转录因子,在SNR6基因的染色质重塑中也起着直接作用。

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