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组蛋白变体H2A.Z的C末端结构域对H2A.Z占据和核小体定位具有位点特异性差异效应。

The Histone Variant H2A.Z C-Terminal Domain Has Locus-Specific Differential Effects on H2A.Z Occupancy and Nucleosome Localization.

作者信息

Neumann Hannah, Jeronimo Celia, Lucier Jean-François, Pasquier Emeline, Robert François, Wellinger Raymund J, Gaudreau Luc

机构信息

Department of Biology, Université de Sherbrooke, Sherbrooke, Quebec, Canada.

Montreal Clinical Research Institute, Montréal, Quebec, Canada.

出版信息

Microbiol Spectr. 2023 Feb 23;11(2):e0255022. doi: 10.1128/spectrum.02550-22.

Abstract

The incorporation of histone variant H2A.Z into nucleosomes creates specialized chromatin domains that regulate DNA-templated processes, such as gene transcription. In Saccharomyces cerevisiae, the diverging H2A.Z C terminus is thought to provide the H2A.Z exclusive functions. To elucidate the roles of this H2A.Z C terminus genome-wide, we used derivatives in which the C terminus was replaced with the corresponding region of H2A (ZA protein), or the H2A region plus a transcriptional activating peptide (ZA-rII'), with the intent of regenerating the H2A.Z-dependent regulation globally. The distribution of these H2A.Z derivatives indicates that the H2A.Z C-terminal region is crucial for both maintaining the occupation level of H2A.Z and the proper positioning of targeted nucleosomes. Interestingly, the specific contribution on incorporation efficiency versus nucleosome positioning varies enormously depending on the locus analyzed. Specifically, the role of H2A.Z in global transcription regulation relies on its C-terminal region. Remarkably, however, this mostly involves genes without a H2A.Z nucleosome in the promoter. Lastly, we demonstrate that the main chaperone complex which deposits H2A.Z to gene regulatory region (SWR1-C) is necessary to localize all H2A.Z derivatives at their specific loci, indicating that the differential association of these derivatives is not due to impaired interaction with SWR1-C. We provide evidence that the Saccharomyces cerevisiae C-terminal region of histone variant H2A.Z can mediate its special function in performing gene regulation by interacting with effector proteins and chaperones. These functional interactions allow H2A.Z not only to incorporate to very specific gene regulatory regions, but also to facilitate the gene expression process. To achieve this, we used a chimeric protein which lacks the native H2A.Z C-terminal region but contains an acidic activating region, a module that is known to interact with components of chromatin-remodeling entities and/or transcription modulators. We reasoned that because this activating region can fulfill the role of the H2A.Z C-terminal region, at least in part, the role of the latter would be to interact with these activating region targets.

摘要

组蛋白变体H2A.Z掺入核小体可形成专门的染色质结构域,调控诸如基因转录等以DNA为模板的过程。在酿酒酵母中,H2A.Z不同的C末端被认为赋予了H2A.Z独特的功能。为了在全基因组范围内阐明该H2A.Z C末端的作用,我们构建了一些衍生物,其中C末端被H2A的相应区域(ZA蛋白)或H2A区域加上一个转录激活肽(ZA-rII')所取代,目的是在整体上重现依赖H2A.Z的调控。这些H2A.Z衍生物的分布表明,H2A.Z C末端区域对于维持H2A.Z的占据水平以及靶向核小体的正确定位都至关重要。有趣的是,根据所分析的基因座,其对掺入效率和核小体定位的具体贡献差异极大。具体而言,H2A.Z在全局转录调控中的作用依赖于其C末端区域。然而,值得注意的是,这主要涉及启动子中没有H2A.Z核小体的基因。最后,我们证明将H2A.Z沉积到基因调控区域的主要伴侣复合物(SWR1-C)对于将所有H2A.Z衍生物定位到其特定基因座是必需的,这表明这些衍生物的差异结合并非由于与SWR1-C的相互作用受损。我们提供的证据表明,酿酒酵母组蛋白变体H2A.Z的C末端区域可通过与效应蛋白和伴侣蛋白相互作用,在执行基因调控中发挥其特殊功能。这些功能相互作用使H2A.Z不仅能够掺入非常特定的基因调控区域,还能促进基因表达过程。为实现这一点,我们使用了一种嵌合蛋白,该蛋白缺乏天然的H2A.Z C末端区域,但含有一个酸性激活区域,该模块已知可与染色质重塑实体和/或转录调节剂的成分相互作用。我们推断,由于这个激活区域至少可以部分履行H2A.Z C末端区域的作用,那么后者的作用将是与这些激活区域的靶点相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/394a/10100702/7b2c0209ba91/spectrum.02550-22-f001.jpg

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