A satellite DNA array barcodes chromosome 7 and regulates totipotency via ZFP819

Author:

Fernandes Liane P.1ORCID,Enriquez-Gasca Rocio1ORCID,Gould Poppy A.1ORCID,Holt James H.1,Conde Lucia2ORCID,Ecco Gabriela3,Herrero Javier2ORCID,Gifford Robert4ORCID,Trono Didier3ORCID,Kassiotis George5ORCID,Rowe Helen M.1ORCID

Affiliation:

1. Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK.

2. Bill Lyons Informatics Centre, UCL Cancer Institute, London WC1E 6BT, UK.

3. School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

4. MRC–University of Glasgow Centre for Virus Research, Glasgow, UK.

5. The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.

Abstract

Mammalian genomes are a battleground for genetic conflict between repetitive elements and KRAB-zinc finger proteins (KZFPs). We asked whether KZFPs can regulate cell fate by using ZFP819, which targets a satellite DNA array, ZP3AR. ZP3AR coats megabase regions of chromosome 7 encompassing genes encoding ZSCAN4, a master transcription factor of totipotency. Depleting ZFP819 in mouse embryonic stem cells (mESCs) causes them to transition to a 2-cell (2C)–like state, whereby the ZP3AR array switches from a poised to an active enhancer state. This is accompanied by a global erosion of heterochromatin roadblocks, which we link to decreased SETDB1 stability. These events result in transcription of active LINE-1 elements and impaired differentiation. In summary, ZFP819 and TRIM28 partner up to close chromatin across Zscan4 , to promote exit from totipotency. We propose that satellite DNAs may control developmental fate transitions by barcoding and switching off master transcription factor genes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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