Univ Paris Est Creteil, INSERM, EnvA, EFS, AP-HP, IMRB, F-94010, Creteil, France.
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Nat Commun. 2021 Jun 8;12(1):3450. doi: 10.1038/s41467-021-23775-9.
The epigenetic mechanisms coordinating the maintenance of adult cellular lineages and the inhibition of alternative cell fates remain poorly understood. Here we show that targeted ablation of the histone chaperone HIRA in myogenic cells leads to extensive transcriptional modifications, consistent with a role in maintaining skeletal muscle cellular identity. We demonstrate that conditional ablation of HIRA in muscle stem cells of adult mice compromises their capacity to regenerate and self-renew, leading to tissue repair failure. Chromatin analysis of Hira-deficient cells show a significant reduction of histone variant H3.3 deposition and H3K27ac modification at regulatory regions of muscle genes. Additionally, we find that genes from alternative lineages are ectopically expressed in Hira-mutant cells via MLL1/MLL2-mediated increase of H3K4me3 mark at silent promoter regions. Therefore, we conclude that HIRA sustains the chromatin landscape governing muscle cell lineage identity via incorporation of H3.3 at muscle gene regulatory regions, while preventing the expression of alternative lineage genes.
表观遗传机制协调成体细胞谱系的维持和抑制替代细胞命运的机制仍知之甚少。在这里,我们表明,在成肌细胞中靶向消融组蛋白伴侣 HIRA 会导致广泛的转录修饰,这与维持骨骼肌细胞特性的作用一致。我们证明,条件性消融成年小鼠肌肉干细胞中的 HIRA 会损害它们的再生和自我更新能力,导致组织修复失败。Hira 缺陷细胞的染色质分析显示,组蛋白变体 H3.3 的沉积和调节区域的 H3K27ac 修饰显著减少肌肉基因。此外,我们发现通过沉默启动子区域的 MLL1/MLL2 介导的 H3K4me3 标记,替代谱系的基因在 Hira 突变细胞中异位表达。因此,我们得出结论,HIRA 通过将 H3.3 整合到肌肉基因调控区域来维持调控肌肉细胞谱系特性的染色质景观,同时防止替代谱系基因的表达。