Zhang Haiying, Roberts Douglas N, Cairns Bradley R
Howard Hughes Medical Institute, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Cell. 2005 Oct 21;123(2):219-31. doi: 10.1016/j.cell.2005.08.036.
Histone variants help specialize chromatin regions; however, their impact on transcriptional regulation is largely unknown. Here, we determined the genome-wide localization and dynamics of Htz1, the yeast histone H2A variant. Htz1 localizes to hundreds of repressed/basal Pol II promoters and prefers TATA-less promoters. Specific Htz1 deposition requires the SWR1 complex, which largely colocalizes with Htz1. Htz1 occupancy correlates with particular histone modifications, and Htz1 deposition is partially reliant on Gcn5 (a histone acetyltransferase) and Bdf1, an SWR1 complex member that binds acetylated histones. Changes in growth conditions cause a striking redistribution of Htz1 from activated to repressed/basal promoters. Furthermore, Htz1 promotes full gene activation but does not generally impact repression. Importantly, Htz1 releases from purified chromatin in vitro under conditions where H2A and H3 remain associated. We suggest that Htz1-bearing nucleosomes are deposited at repressed/basal promoters but facilitate activation through their susceptibility to loss, thereby helping to expose promoter DNA.
组蛋白变体有助于使染色质区域特化;然而,它们对转录调控的影响在很大程度上尚不清楚。在这里,我们确定了酵母组蛋白H2A变体Htz1在全基因组范围内的定位和动态变化。Htz1定位于数百个受抑制/基础的Pol II启动子,且更倾向于无TATA盒的启动子。特定的Htz1沉积需要SWR1复合物,该复合物在很大程度上与Htz1共定位。Htz1的占据与特定的组蛋白修饰相关,并且Htz1的沉积部分依赖于Gcn5(一种组蛋白乙酰转移酶)和Bdf1,Bdf1是SWR1复合物的一个成员,可结合乙酰化组蛋白。生长条件的变化导致Htz1从激活的启动子显著重新分布到受抑制/基础的启动子。此外,Htz1促进基因的完全激活,但通常不影响基因抑制。重要的是,在H2A和H3仍保持结合的条件下,Htz1在体外从纯化的染色质中释放出来。我们认为,含有Htz1的核小体沉积在受抑制/基础的启动子上,但通过它们对丢失的敏感性促进激活,从而有助于暴露启动子DNA。