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H3K4me2 and WDR5 enriched chromatin interacting long non-coding RNAs maintain transcriptionally competent chromatin at divergent transcriptional units

机译:H3K4me2和WDR5富集的染色质相互作用的长非编码RNA维持在不同转录单位的转录能力染色质

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摘要

Recently lncRNAs have been implicated in the sub-compartmentalization of eukaryotic genome via genomic targeting of chromatin remodelers. To explore the function of lncRNAs in the maintenance of active chromatin, we characterized lncRNAs from the chromatin enriched with H3K4me2 and WDR5 using chromatin RNA immunoprecipitation (ChRIP). Significant portion of these enriched lncRNAs were arranged in antisense orientation with respect to their protein coding partners. Among these, 209 lncRNAs, commonly enriched in H3K4me2 and WDR5 chromatin fractions, were named as active chromatin associated lncRNAs (active lncCARs). Interestingly, 43% of these active lncCARs map to divergent transcription units. Divergent transcription (XH) units were overrepresented in the active lncCARs as compared to the inactive lncCARs. ChIP-seq analysis revealed that active XH transcription units are enriched with H3K4me2, H3K4me3 and WDR5. WDR5 depletion resulted in the loss of H3K4me3 but not H3K4me2 at the XH promoters. Active XH CARs interact with and recruit WDR5 to XH promoters, and their depletion leads to decrease in the expression of the corresponding protein coding genes and loss of H3K4me2, H3K4me3 and WDR5 at the active XH promoters. This study unravels a new facet of chromatin-based regulation at the divergent XH transcription units by this newly identified class of H3K4me2/WDR5 chromatin enriched lncRNAs.
机译:最近,lncRNA已经通过染色质重塑剂的基因组靶向作用参与了真核生物基因组的亚室化。为了探索lncRNA在活性染色质维持中的功能,我们使用染色质RNA免疫沉淀法(ChRIP)从富含H3K4me2和WDR5的染色质中鉴定了lncRNAs。这些富集的lncRNA的重要部分相对于其蛋白编码伴侣以反义方向排列。其中,通常富含H3K4me2和WDR5染色质组分的209个lncRNA被称为与活性染色质相关的lncRNA(活性lncCAR)。有趣的是,这些活性lncCAR中有43%映射到不同的转录单位。与不活跃的lncCAR相比,活跃的lncCAR中的差异转录(XH)单位过多。 ChIP-seq分析显示,活跃的XH转录单元富含H3K4me2,H3K4me3和WDR5。 WDR5耗尽导致XH启动子丢失H3K4me3,但没有丢失H3K4me2。活跃的XH CAR与XDR启动子相互作用并将WDR5募集到XH启动子,并且它们的耗竭导致相应蛋白质编码基因的表达减少,以及活跃XH启动子处的H3K4me2,H3K4me3和WDR5丢失。这项研究通过这种新鉴定的富含H3K4me2 / WDR5染色质的lncRNA,揭示了在不同的XH转录单位上基于染色质的调控的新方面。

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