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PCGF6-PRC1 suppresses premature differentiation of mouse embryonic stem cells by regulating germ cell-related genes

机译:PCGF6-PRC1通过调节生殖细胞相关基因抑制小鼠胚胎干细胞的过早分化

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摘要

The ring finger protein PCGF6 (polycomb group ring finger 6) interacts with RING1A/B and E2F6 associated factors to form a non-canonical PRC1 (polycomb repressive complex 1) known as PCGF6-PRC1. Here, we demonstrate that PCGF6-PRC1 plays a role in repressing a subset of PRC1 target genes by recruiting RING1B and mediating downstream mono-ubiquitination of histone H2A. PCGF6-PRC1 bound loci are highly enriched for promoters of germ cell-related genes in mouse embryonic stem cells (ESCs). Conditional ablation of Pcgf6 in ESCs leads to robust de-repression of such germ cell-related genes, in turn affecting cell growth and viability. We also find a role for PCGF6 in pre- and peri-implantation mouse embryonic development. We further show that a heterodimer of the transcription factors MAX and MGA recruits PCGF6 to target loci. PCGF6 thus links sequence specific target recognition by the MAX/MGA complex to PRC1-dependent transcriptional silencing of germ cell-specific genes in pluripotent stem cells.
机译:无名指蛋白PCGF6(聚梳组无名指6)与RING1A / B和E2F6相关因子相互作用,形成称为PCGF6-PRC1的非规范PRCC1(聚梳抑制复合物1)。在这里,我们证明PCGF6-PRC1在通过募集RING1B并介导组蛋白H2A的下游单泛素化来抑制PRC1目标基因的一个子集中。 PCGF6-PRC1绑定的基因座是小鼠胚胎干细胞(ESC)中生殖细胞相关基因启动子的高度富集。 ESC中Pcgf6的条件消融可导致此类生殖细胞相关基因的强烈抑制,进而影响细胞生长和生存能力。我们还发现PCGF6在植入前和植入前小鼠胚胎发育中的作用。我们进一步表明,转录因子MAX和MGA的异二聚体募集PCGF6到靶基因座。因此,PCGF6将MAX / MGA复合物的序列特异性靶标识别与多能干细胞中生殖细胞特异性基因的PRC1依赖性转录沉默联系起来。

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