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XB-ART-51677
Nat Commun January 20, 2015; 6 10148.

Embryonic transcription is controlled by maternally defined chromatin state.

Hontelez S , van Kruijsbergen I , Georgiou G , van Heeringen SJ , Bogdanovic O , Lister R , Veenstra GJ .


Abstract
Histone-modifying enzymes are required for cell identity and lineage commitment, however little is known about the regulatory origins of the epigenome during embryonic development. Here we generate a comprehensive set of epigenome reference maps, which we use to determine the extent to which maternal factors shape chromatin state in Xenopus embryos. Using α-amanitin to inhibit zygotic transcription, we find that the majority of H3K4me3- and H3K27me3-enriched regions form a maternally defined epigenetic regulatory space with an underlying logic of hypomethylated islands. This maternal regulatory space extends to a substantial proportion of neurula stage-activated promoters. In contrast, p300 recruitment to distal regulatory regions requires embryonic transcription at most loci. The results show that H3K4me3 and H3K27me3 are part of a regulatory space that exerts an extended maternal control well into post-gastrulation development, and highlight the combinatorial action of maternal and zygotic factors through proximal and distal regulatory sequences.

PubMed ID: 26679111
PMC ID: PMC4703837
Article link: Nat Commun
Grant support: R01HD069344 NICHD NIH HHS , R01 HD069344 NICHD NIH HHS

Genes referenced: crebbp gbx2.1 gbx2.2


External Resources:
Article Images: [+] show captions

References:
Akkers, 2009, Pubmed, Xenbase [+]


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