From the Department of Oncology and.
the Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201.
J Biol Chem. 2018 Sep 28;293(39):15120-15135. doi: 10.1074/jbc.RA118.004974. Epub 2018 Aug 16.
RNA has been shown to interact with various proteins to regulate chromatin dynamics and gene expression. However, it is unknown whether RNAs associate with epigenetic marks such as post-translational modifications of histones, including histone 4 lysine 20 trimethylation (H4K20me3) or trimethylated histone 3 lysine 4 (H3K4me3), to regulate chromatin and gene expression. Here, we used chromatin-associated RNA immunoprecipitation (CARIP) followed by next-generation sequencing (CARIP-Seq) to survey RNAs associated with H4K20me3- and H3K4me3-marked chromatin on a global scale in embryonic stem (ES) cells. We identified thousands of mRNAs and noncoding RNAs that associate with H4K20me3- and H3K4me3-marked chromatin. H4K20me3- and H3K4me3-interacting RNAs are involved in chromatin organization and modification and RNA processing, whereas H4K20me3-only RNAs are involved in cell motility and differentiation, and H3K4me3-only RNAs are involved in metabolic processes and RNA processing. Expression of H3K4me3-associated RNAs is enriched in ES cells, whereas expression of H4K20me3-associated RNAs is enriched in ES cells and differentiated cells. H4K20me3- and H3K4me3-interacting RNAs originate from genes that co-localize with features of active chromatin, including transcriptional machinery and active promoter regions, and the histone modification H3K36me3 in gene body regions. We also found that H4K20me3 and H3K4me3 are associated with distinct gene features including transcripts of greater length and exon number relative to unoccupied transcripts. H4K20me3- and H3K4me3-marked chromatin is also associated with processed RNAs (exon transcripts) relative to unspliced pre-mRNA and ncRNA transcripts. In summary, our results provide evidence that H4K20me3- and H3K4me3-associated RNAs represent a distinct subnetwork of the ES cell transcriptional repertoire.
RNA 已被证明与各种蛋白质相互作用,以调节染色质动力学和基因表达。然而,目前尚不清楚 RNA 是否与组蛋白的翻译后修饰(包括组蛋白 4 赖氨酸 20 三甲基化(H4K20me3)或三甲基化组蛋白 3 赖氨酸 4(H3K4me3))等表观遗传标记结合,以调节染色质和基因表达。在这里,我们使用染色质相关 RNA 免疫沉淀(CARIP),然后进行下一代测序(CARIP-Seq),在胚胎干细胞(ES 细胞)中对与 H4K20me3 和 H3K4me3 标记的染色质相关的 RNA 进行了全面的调查。我们鉴定了数千个与 H4K20me3 和 H3K4me3 标记的染色质结合的 mRNA 和非编码 RNA。H4K20me3 和 H3K4me3 相互作用的 RNA 参与染色质组织和修饰以及 RNA 处理,而 H4K20me3 仅 RNA 参与细胞运动和分化,H3K4me3 仅 RNA 参与代谢过程和 RNA 处理。H3K4me3 相关 RNA 的表达在 ES 细胞中富集,而 H4K20me3 相关 RNA 的表达在 ES 细胞和分化细胞中富集。H4K20me3 和 H3K4me3 相互作用的 RNA 来自与活跃染色质特征(包括转录机制和活性启动子区域)以及基因体区域的组蛋白修饰 H3K36me3 共定位的基因。我们还发现 H4K20me3 和 H3K4me3 与不同的基因特征相关,包括与未占据的转录本相比具有更长和更多外显子的转录本。H4K20me3 和 H3K4me3 标记的染色质也与加工 RNA(外显子转录本)相关,而与未剪接的前体 RNA 和 ncRNA 转录本相比。总之,我们的研究结果为 H4K20me3 和 H3K4me3 相关 RNA 代表 ES 细胞转录组的一个独特的子网络提供了证据。