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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:基础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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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。相比之下,由于TFIIIB直接识别 SNR6 TATA盒,TFIIIC对体外纯化成分的 SNR6 转录几乎没有影响。当使用 Drosophila melanogaster S-190提取物将 SNR6 体外组装到染色质中时,这些模板在高纯度酵母pol III,TFIIIC和TFIIIB的转录下显示出几乎达到TFIIIC的绝对要求,但相对于裸露的DNA产生了5至15倍高的转录水平(比抑制的染色质活化> 100倍)。染色质结构的分析表明,TFIIIC结合导致U6基因染色质的重塑,从而导致核小体位于框A和B之间。插入的DNA折叠进入核小体中会导致亚最佳间隔的 SNR6 框A和B的元素更接近,因此有助于转录的激活。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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