Polycomb group proteins Ring1A/B are functionally linked to the core transcriptional regulatory circuitry to maintain ES cell identity

Author:

Endoh Mitsuhiro1,Endo Takaho A.2,Endoh Tamie1,Fujimura Yu-ichi1,Ohara Osamu1,Toyoda Tetsuro2,Otte Arie P.3,Okano Masaki4,Brockdorff Neil5,Vidal Miguel16,Koseki Haruhiko1

Affiliation:

1. RIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro, Tsurumi-ku,Yokohama 230-0045, Japan.

2. RIKEN Genomic Sciences Center, 1-7-22 Suehiro, Tsurumi-ku, Yokohama 230-0045,Japan.

3. Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 406, 1098 SM Amsterdam, The Netherlands.

4. RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku,Kobe, Hyogo 6500047, Japan.

5. Developmental Epigenetics Group, MRC Clinical Sciences Centre, ICFM,Hammersmith Hospital, DuCane Road, London W12 ONN, UK.

6. Centro de Investigaciones Biologicas, Department of Developmental and Cell Biology, Ramiro de Maeztu 9, 28040 Madrid, Spain.

Abstract

The Polycomb group (PcG) proteins mediate heritable silencing of developmental regulators in metazoans, participating in one of two distinct multimeric protein complexes, the Polycomb repressive complexes 1 (PRC1) and 2(PRC2). Although PRC2 has been shown to share target genes with the core transcription network, including Oct3/4, to maintain embryonic stem (ES)cells, it is still unclear whether PcG proteins and the core transcription network are functionally linked. Here, we identify an essential role for the core PRC1 components Ring1A/B in repressing developmental regulators in mouse ES cells and, thereby, in maintaining ES cell identity. A significant proportion of the PRC1 target genes are also repressed by Oct3/4. We demonstrate that engagement of PRC1 at target genes is Oct3/4-dependent,whereas engagement of Oct3/4 is PRC1-independent. Moreover, upon differentiation induced by Gata6 expression, most of the Ring1A/B target genes are derepressed and the binding of Ring1A/B to their target loci is also decreased. Collectively, these results indicate that Ring1A/B-mediated Polycomb silencing functions downstream of the core transcriptional regulatory circuitry to maintain ES cell identity.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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