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

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 recruiti...

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Detalles Bibliográficos
Autores principales: Endoh, Mitsuhiro, Endo, Takaho A, Shinga, Jun, Hayashi, Katsuhiko, Farcas, Anca, Ma, Kit-Wan, Ito, Shinsuke, Sharif, Jafar, Endoh, Tamie, Onaga, Naoko, Nakayama, Manabu, Ishikura, Tomoyuki, Masui, Osamu, Kessler, Benedikt M, Suda, Toshio, Ohara, Osamu, Okuda, Akihiko, Klose, Robert, Koseki, Haruhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375644/
https://www.ncbi.nlm.nih.gov/pubmed/28304275
http://dx.doi.org/10.7554/eLife.21064
Descripción
Sumario: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. DOI: http://dx.doi.org/10.7554/eLife.21064.001