期刊
MOLECULAR CELL
卷 47, 期 6, 页码 909-920出版社
CELL PRESS
DOI: 10.1016/j.molcel.2012.07.010
关键词
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资金
- European Young Investigator Award (EURYI)
- Fondation Schlumberger
- BBSRC [BB/G00711X/1]
- Wellcome Trust [085448/Z/08/Z]
- ARC
- Institut Curie, S.A.
- Canceropole Ile-de-France
- RCUK
- Biotechnology and Biological Sciences Research Council [BB/G00711X/1] Funding Source: researchfish
- Engineering and Physical Sciences Research Council [836374] Funding Source: researchfish
- BBSRC [BB/G00711X/1] Funding Source: UKRI
- Wellcome Trust [085448/Z/08/Z] Funding Source: Wellcome Trust
Identifying loci with parental differences in DNA methylation is key to unraveling parent-of-origin phenotypes. By conducting a MeDIP-Seq screen in maternal-methylation free postimplantation mouse embryos (Dnmt3L-/+), we demonstrate that maternal-specific methylation exists very scarcely at midgestation. We reveal two forms of oocyte-specific methylation inheritance: limited to preimplantation, or with longer duration, i.e. maternally imprinted loci. Transient and imprinted maternal germline DMRs (gDMRs) are indistinguishable in gametes and preimplantation embryos, however, de novo methylation of paternal alleles at implantation delineates their fates and acts as a major leveling factor of parent-inherited differences. We characterize two new imprinted gDMRs, at the Cdh15 and AK008011 loci, with tissue-specific imprinting loss, again by paternal methylation gain. Protection against demethylation after fertilization has been emphasized as instrumental in maintaining parent-of-origin methylation inherited from the gametes. Here we provide evidence that protection against de novo methylation acts as an equal major pivot, at implantation and throughout life.
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