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染色质重塑因子 Ino80C 独立于 H2A.Z 发挥作用,可驱逐启动子核小体并刺激酵母中高表达基因的转录。

Chromatin remodeler Ino80C acts independently of H2A.Z to evict promoter nucleosomes and stimulate transcription of highly expressed genes in yeast.

机构信息

Division of Molecular and Cellular Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Department of Biological Sciences, Oakland University, Rochester, MI 48309, USA.

出版信息

Nucleic Acids Res. 2020 Sep 4;48(15):8408-8430. doi: 10.1093/nar/gkaa571.

Abstract

The chromatin remodelers SWI/SNF and RSC function in evicting promoter nucleosomes at highly expressed yeast genes, particularly those activated by transcription factor Gcn4. Ino80 remodeling complex (Ino80C) can establish nucleosome-depleted regions (NDRs) in reconstituted chromatin, and was implicated in removing histone variant H2A.Z from the -1 and +1 nucleosomes flanking NDRs; however, Ino80C's function in transcriptional activation in vivo is not well understood. Analyzing the cohort of Gcn4-induced genes in ino80Δ mutants has uncovered a role for Ino80C on par with SWI/SNF in evicting promoter nucleosomes and transcriptional activation. Compared to SWI/SNF, Ino80C generally functions over a wider region, spanning the -1 and +1 nucleosomes, NDR and proximal genic nucleosomes, at genes highly dependent on its function. Defects in nucleosome eviction in ino80Δ cells are frequently accompanied by reduced promoter occupancies of TBP, and diminished transcription; and Ino80 is enriched at genes requiring its remodeler activity. Importantly, nuclear depletion of Ino80 impairs promoter nucleosome eviction even in a mutant lacking H2A.Z. Thus, Ino80C acts widely in the yeast genome together with RSC and SWI/SNF in evicting promoter nucleosomes and enhancing transcription, all in a manner at least partly independent of H2A.Z editing.

摘要

染色质重塑因子 SWI/SNF 和 RSC 可在高表达的酵母基因中去除启动子核小体,特别是那些被转录因子 Gcn4 激活的基因。Ino80 重塑复合物(Ino80C)可在重组染色质中建立无核小体区域(NDR),并被认为可将组蛋白变体 H2A.Z 从 NDR 侧翼的-1 和+1 核小体中去除;然而,Ino80C 在体内转录激活中的功能尚未得到很好的理解。在 ino80Δ 突变体中分析 Gcn4 诱导的基因队列时,发现 Ino80C 在去除启动子核小体和转录激活方面与 SWI/SNF 具有同等作用。与 SWI/SNF 相比,Ino80C 通常在更广泛的区域起作用,跨越-1 和+1 核小体、NDR 和近端基因核小体,在高度依赖其功能的基因上。在 ino80Δ 细胞中,核小体驱逐缺陷通常伴随着 TBP 启动子占有率降低和转录减少;并且 Ino80 富集在需要其重塑酶活性的基因上。重要的是,即使在缺乏 H2A.Z 的突变体中,Ino80 的核内耗竭也会损害启动子核小体的驱逐。因此,Ino80C 与 RSC 和 SWI/SNF 一起广泛作用于酵母基因组,以去除启动子核小体并增强转录,至少在某种程度上独立于 H2A.Z 编辑。

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