Epigenetic Dynamics of Imprinted X Inactivation During Early Mouse Development
Epigenetic Dynamics of Imprinted X Inactivation During Early Mouse Development
The initiation of X-chromosome inactivation is thought to be tightly correlated with early differentiation events during mouse development. Here, we show that although initially active, the paternal X chromosome undergoes imprinted inactivation from the cleavage stages, well before cellular differentiation. A reversal of the inactive state, with a loss of epigenetic marks such as histone modifications and polycomb proteins, subsequently occurs in cells of the inner cell mass (ICM), which give rise to the embryo-proper in which random X inactivation is known to occur. This reveals the remarkable plasticity of the X-inactivation process during preimplantation development and underlines the importance of the ICM in global reprogramming of epigenetic marks in the early embryo.
- Rockefeller University United States
- Howard Hughes Medical Institute United States
- Centre national de la recherche scientifique France
- Institute Curie France
- University of Medicine and Dentistry of New Jersey United States
Male, 570, Blastomeres, RNA, Untranslated, Transcription, Genetic, 610, Acetylation, Embryo, Mammalian, Chromosomes, Mammalian, Methylation, Morula, Chromatin, Epigenesis, Genetic, Histones, Embryonic and Fetal Development, Genomic Imprinting, Mice, Blastocyst, Dosage Compensation, Genetic, Animals, Female, RNA, Long Noncoding
Male, 570, Blastomeres, RNA, Untranslated, Transcription, Genetic, 610, Acetylation, Embryo, Mammalian, Chromosomes, Mammalian, Methylation, Morula, Chromatin, Epigenesis, Genetic, Histones, Embryonic and Fetal Development, Genomic Imprinting, Mice, Blastocyst, Dosage Compensation, Genetic, Animals, Female, RNA, Long Noncoding
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