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FACT and Asf1 regulate nucleosome dynamics and coactivator binding at the HO promoter.

机译:FACT和Asf1调节HO启动子处的核小体动力学和共激活因子结合。

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Transcriptional activators and coactivators overcome repression by chromatin, but regulation of chromatin disassembly and coactivator binding to promoters is poorly understood. Activation of the yeast HO gene follows the sequential binding of both sequence-specific DNA-binding proteins and coactivators during the cell cycle. Here, we show that the nucleosome disassembly occurs in waves both along the length of the promoter and during the cell cycle. Different chromatin modifiers are required for chromatin disassembly at different regions of the promoter, with Swi/Snf, the FACT chromatin reorganizer, and the Asf1 histone chaperone each required for nucleosome eviction at distinct promoter regions. FACT and Asf1 both bind to upstream elements of the HO promoter well before the gene is transcribed. The Swi/Snf, SAGA, and Mediator coactivators bind first to the far upstream promoter region and subsequently to a promoter proximal region, and FACT and Asf1 are both required for this coactivator re-recruitment.
机译:转录激活剂和共激活剂克服了染色质的阻抑作用,但对染色质分解和共激活剂与启动子结合的调控了解甚少。酵母HO基因的激活遵循序列特异性DNA结合蛋白和共激活因子在细胞周期中的顺序结合。在这里,我们表明核小体的分解发生在沿启动子的长度和细胞周期中的波中。在启动子的不同区域进行染色质拆卸需要使用不同的染色质修饰剂,而Swi / Snf,FACT染色质重组剂和Asf1组蛋白分子伴侣则需要在不同的启动子区域逐出核小体。 FACT和Asf1都早在基因转录前就与HO启动子的上游元件结合。 Swi / Snf,SAGA和介体共激活因子首先与远上游启动子区域结合,然后与启动子近端区域结合,并且该共激活因子的重新招募都需要FACT和Asf1。

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