Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84112, USA.
Nucleic Acids Res. 2020 Nov 4;48(19):10877-10889. doi: 10.1093/nar/gkaa819.
The Saccharomyces cerevisiae HO gene is a model regulatory system with complex transcriptional regulation. Budding yeast divide asymmetrically and HO is expressed only in mother cells where a nucleosome eviction cascade along the promoter during the cell cycle enables activation. HO expression in daughter cells is inhibited by high concentration of Ash1 in daughters. To understand how Ash1 represses transcription, we used a myo4 mutation which boosts Ash1 accumulation in both mothers and daughters and show that Ash1 inhibits promoter recruitment of SWI/SNF and Gcn5. We show Ash1 is also required for the efficient nucleosome repopulation that occurs after eviction, and the strongest effects of Ash1 are seen when Ash1 has been degraded and at promoter locations distant from where Ash1 bound. Additionally, we defined a specific nucleosome/nucleosome-depleted region structure that restricts HO activation to one of two paralogous DNA-binding factors. We also show that nucleosome eviction occurs bidirectionally over a large distance. Significantly, eviction of the more distant nucleosomes is dependent upon the FACT histone chaperone, and FACT is recruited to these regions when eviction is beginning. These last observations, along with ChIP experiments involving the SBF factor, suggest a long-distance loop transiently forms at the HO promoter.
酿酒酵母 HO 基因是一个具有复杂转录调控的模型调控系统。芽殖酵母不对称分裂,HO 仅在母细胞中表达,在细胞周期中,核小体沿着启动子发生驱逐级联,从而激活 HO 的表达。高浓度的 Ash1 在子细胞中抑制 HO 的表达。为了理解 Ash1 如何抑制转录,我们利用了一个 myo4 突变,该突变增强了 Ash1 在母细胞和子细胞中的积累,并表明 Ash1 抑制了 SWI/SNF 和 Gcn5 对启动子的募集。我们还表明,Ash1 对于驱逐后发生的核小体重新填充是必需的,并且当 Ash1 降解时以及在远离 Ash1 结合位置的启动子位置,Ash1 的影响最强。此外,我们定义了一种特定的核小体/核小体缺失区域结构,将 HO 的激活限制在两个同源 DNA 结合因子之一上。我们还表明,核小体驱逐是双向发生的,跨越了很大的距离。重要的是,更远的核小体的驱逐依赖于 FACT 组蛋白伴侣,并且当驱逐开始时,FACT 被招募到这些区域。这些最后的观察结果,以及涉及 SBF 因子的 ChIP 实验表明,在 HO 启动子处形成了一个长距离环。