Telomeres and Telomerase Group, Molecular Oncology Program, Melchor Fernández Almagro 3, E-28029, Madrid, Spain.
Confocal Microscopy Unit, Spanish National Cancer Centre (CNIO), Melchor Fernández Almagro 3, E-28029, Madrid, Spain.
Nat Commun. 2018 Apr 18;9(1):1548. doi: 10.1038/s41467-018-03916-3.
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.
TERRAs 是从端粒产生的长非编码 RNA。缺乏 TERRA 敲除模型阻碍了对 TERRA 功能的理解。我们最近确定了 20 号染色体是人类 TERRA 的主要起源之一,这使我们能够生成第一个 20q-TERRA 敲除模型,并证明 TERRA 对于端粒长度维持和保护是必不可少的。在这里,我们使用 ALT 20q-TERRA 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-TERRA 对于在端粒处建立 H3K9me3、H4K20me3 和 H3K27me3 异染色质标记至关重要。在机制水平上,我们发现 TERRA 与负责催化 H3K27 三甲基化的 PRC2 结合,并且其定位于端粒依赖于 TERRA。我们进一步证明端粒处 PRC2 依赖性 H3K27me3 对于在端粒处建立 H3K9me3、H4K20me3 和 HP1 结合是必需的。总之,这些发现表明 TERRA 在端粒异染色质组装中起着重要作用。