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

Author:

Endoh Mitsuhiro12345ORCID,Endo Takaho A6,Shinga Jun7,Hayashi Katsuhiko8,Farcas Anca9,Ma Kit-Wan1,Ito Shinsuke12,Sharif Jafar12,Endoh Tamie135,Onaga Naoko1,Nakayama Manabu10,Ishikura Tomoyuki1,Masui Osamu1,Kessler Benedikt M11,Suda Toshio34,Ohara Osamu610,Okuda Akihiko12ORCID,Klose Robert9ORCID,Koseki Haruhiko12ORCID

Affiliation:

1. Laboratory for Developmental Genetics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan

2. Core Research for Evolutional Science and Technology, Yokohama, Japan

3. Centre for Translational Medicine,Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore

4. International Research Center for Medical Sciences, Kumamoto University, Kumamoto, Japan

5. Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan

6. Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan

7. Laboratory for Immunotherapy, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan

8. Department of Developmental Stem Cell Biology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan

9. Department of Biochemistry, Oxford University, Oxford, United Kingdom

10. Chromosome Engineering Team, Department of Technology Development, Kazusa DNA Research Institute, Kisarazu, Japan

11. Mass Spectrometry Laboratory, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

12. Division of Developmental Biology, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan

Abstract

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.

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Ministry of Education, Culture, Sports, Science and Technology

RIKEN

Japan Science and Technology Agency

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference52 articles.

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