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TERRA recruitment of polycomb to telomeres is essential for histone trymethylation marks at telomeric heterochromatin

机译:端粒异端的TERRA募集对端粒异染色质上组蛋白的甲基化标记至关重要

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摘要

TERRAs are long non-coding RNAs generated from the telomeres. Lack of TERRA knockout models has hampered understanding TERRAs’ functions. We recently identified chromosome 20q as one of the main origins of human TERRAs, allowing us to generate the first 20q-TERRA knockout models and to demonstrate that TERRAs are essential for telomere length maintenance and protection. Here, we use ALT 20q-TERRA knockout cells to address a direct role of TERRAs in telomeric heterochromatin formation. We find that 20q-TERRAs are essential for the establishment of H3K9me3, H4K20me3, and H3K27me3 heterochromatin marks at telomeres. At the mechanistic level, we find that TERRAs bind to PRC2, responsible for catalyzing H3K27 tri-methylation, and that its localization to telomeres is TERRA-dependent. We further demonstrate that PRC2-dependent H3K27me3 at telomeres is required for the establishment of H3K9me3, H4K20me3, and HP1 binding at telomeres. Together, these findings demonstrate an important role for TERRAs in telomeric heterochromatin assembly.
机译:TERRA是从端粒产生的长的非编码RNA。缺少TERRA淘汰模型妨碍了对TERRA功能的理解。我们最近将20q染色体鉴定为人类TERRA的主要来源之一,这使我们能够生成第一个20q-TERRA基因敲除模型,并证明TERRA对端粒长度的维持和保护至关重要。在这里,我们使用ALT 20q-TERRA基因敲除细胞来解决TERRA在端粒异染色质形成中的直接作用。我们发现20q-TERRAs对于在端粒建立H3K9me3,H4K20me3和H3K27me3异染色质标记至关重要。在机制水平上,我们发现TERRAs与PRC2结合,负责催化H3K27三甲基化,并且其定位于端粒是TERRA依赖性的。我们进一步证明端粒上依赖PRC2的H3K27me3是建立端粒H3K9me3,H4K20me3和HP1结合所必需的。总之,这些发现证明了TERRA在端粒异染色质组装中的重要作用。

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