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The Dynamics of Genome-wide DNA Methylation Reprogramming in Mouse Primordial Germ Cells

by: Stefanie Seisenberger, Simon Andrews, Felix Krueger, Julia Arand, Jörn Walter, Fátima Santos, Christian Popp, Bernard Thienpont, Wendy Dean, Wolf Reik
Mol Cell, Vol. 48, No. 6. (28 December 2012), pp. 849-862, doi:10.1016/j.molcel.2012.11.001  Key: citeulike:11841975

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Abstract

Genome-wide DNA methylation reprogramming occurs in mouse primordial germ cells (PGCs) and preimplantation embryos, but the precise dynamics and biological outcomes are largely unknown. We have carried out whole-genome bisulfite sequencing (BS-Seq) and RNA-Seq across key stages from E6.5 epiblast to E16.5 PGCs. Global loss of methylation takes place during PGC expansion and migration with evidence for passive demethylation, but sequences that carry long-term epigenetic memory (imprints, CpG islands on the X chromosome, germline-specific genes) only become demethylated upon entry of PGCs into the gonads. The transcriptional profile of PGCs is tightly controlled despite global hypomethylation, with transient expression of the pluripotency network, suggesting that reprogramming and pluripotency are inextricably linked. Our results provide a framework for the understanding of the epigenetic ground state of pluripotency in the germline. º DNA demethylation in PGCs occurs in two phases º Global loss of methylation reveals evidence for a passive demethylation mechanism º Global methylation erasure coincides with expression of the pluripotency network º VECs (variably erased CGIs) may act as carriers of transgenerational inheritance


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