Adkins Melissa W, Williams Stephanie K, Linger Jeffrey, Tyler Jessica K
Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, Colorado 80045, USA.
Mol Cell Biol. 2007 Sep;27(18):6372-82. doi: 10.1128/MCB.00981-07. Epub 2007 Jul 9.
The disassembly of promoter nucleosomes appears to be a general property of highly transcribed eukaryotic genes. We have previously shown that the disassembly of chromatin from the promoters of the Saccharomyces cerevisiae PHO5 and PHO8 genes, mediated by the histone chaperone anti-silencing function 1 (Asf1), is essential for transcriptional activation upon phosphate depletion. This mechanism of transcriptional regulation is shared with the ADY2 and ADH2 genes upon glucose removal. Promoter chromatin disassembly by Asf1 is required for recruitment of TBP and RNA polymerase II, but not the Pho4 and Pho2 activators. Furthermore, accumulation of SWI/SNF and SAGA at the PHO5 promoter requires promoter chromatin disassembly. By contrast, the requirement for SWI/SNF and SAGA to facilitate Pho4 activator recruitment to the nucleosome-buried binding site in the PHO5 promoter occurs prior to chromatin disassembly and is distinct from the stable recruitment of SWI/SNF and SAGA that occurs after chromatin disassembly.
启动子核小体的解体似乎是高度转录的真核基因的一个普遍特性。我们之前已经表明,由组蛋白伴侣抗沉默功能1(Asf1)介导的酿酒酵母PHO5和PHO8基因启动子处染色质的解体,对于磷酸盐耗尽时的转录激活至关重要。这种转录调控机制在去除葡萄糖后与ADY2和ADH2基因相同。Asf1介导的启动子染色质解体是TBP和RNA聚合酶II募集所必需的,但不是Pho4和Pho2激活因子募集所必需的。此外,SWI/SNF和SAGA在PHO5启动子处的积累需要启动子染色质解体。相比之下,SWI/SNF和SAGA促进Pho4激活因子募集到PHO5启动子中核小体掩埋的结合位点的需求发生在染色质解体之前,并且与染色质解体后发生的SWI/SNF和SAGA的稳定募集不同。