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The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription

机译:酵母中的组蛋白变体H2A.Z几乎仅沿转录方向掺入+1核小体中

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摘要

Transcription start sites (TSS) in eukaryotes are characterized by a nucleosome-depleted region (NDR), which appears to be flanked upstream and downstream by strongly positioned nucleosomes incorporating the histone variant H2A.Z. H2A.Z associates with both active and repressed TSS and is important for priming genes for rapid transcriptional activation. However, the determinants of H2A.Z occupancy at specific nucleosomes and its relationship to transcription initiation remain unclear. To further elucidate the specificity of H2A.Z, we determined its genomic localization at single nucleosome resolution, as well as the localization of its chromatin remodelers Swr1 and Ino80. By analyzing H2A.Z occupancy in conjunction with RNA expression data that captures promoter-derived antisense initiation, we find that H2A.Z’s bimodal incorporation on either side of the NDR is not a general feature of TSS, but is specifically a marker for bidirectional transcription, such that the upstream flanking −1 H2A.Z-containing nucleosome is more appropriately considered as a +1 H2A.Z nucleosome for antisense transcription. The localization of H2A.Z almost exclusively at the +1 nucleosome suggests that a transcription-initiation dependent process could contribute to its specific incorporation.
机译:真核生物中的转录起始位点(TSS)的特征是核小体耗尽区(NDR),该区域似乎位于上游和下游,侧翼是结合有组蛋白变体H2A.Z的牢固定位的核小体。 H2A.Z与活跃的TSS和受抑制的TSS都相关,并且对于启动快速转录激活的基因很重要。但是,尚不清楚H2A.Z在特定核小体上的占有率及其与转录起始的关系的决定因素。为了进一步阐明H2A.Z的特异性,我们确定了其在单核小体分辨率下的基因组定位,以及其染色质重塑剂Swr1和Ino80的定位。通过分析H2A.Z的占有率以及捕获启动子衍生的反义起始的RNA表达数据,我们发现H2A.Z在NDR两侧的双峰掺入不是TSS的一般特征,而是专门用于双向转录的标记,使得上游侧翼含-1 H2A.Z的核小体更适合被认为是用于反义转录的+1 H2A.Z核小体。 H2A.Z几乎完全位于+1核小体上,这表明转录起始依赖性过程可能有助于其特异性掺入。

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