| Literature DB >> 25220291 |
Fan Guo1, Xianlong Li2, Dan Liang3, Tong Li4, Ping Zhu2, Hongshan Guo2, Xinglong Wu2, Lu Wen2, Tian-Peng Gu4, Boqiang Hu2, Colum P Walsh5, Jinsong Li6, Fuchou Tang7, Guo-Liang Xu8.
Abstract
The epigenomes of mammalian sperm and oocytes, characterized by gamete-specific 5-methylcytosine (5mC) patterns, are reprogrammed during early embryogenesis to establish full developmental potential. Previous studies have suggested that the paternal genome is actively demethylated in the zygote while the maternal genome undergoes subsequent passive demethylation via DNA replication during cleavage. Active demethylation is known to depend on 5mC oxidation by Tet dioxygenases and excision of oxidized bases by thymine DNA glycosylase (TDG). Here we show that both maternal and paternal genomes undergo widespread active and passive demethylation in zygotes before the first mitotic division. Passive demethylation was blocked by the replication inhibitor aphidicolin, and active demethylation was abrogated by deletion of Tet3 in both pronuclei. At actively demethylated loci, 5mCs were processed to unmodified cytosines. Surprisingly, the demethylation process was unaffected by the deletion of TDG from the zygote, suggesting the existence of other demethylation mechanisms downstream of Tet3-mediated oxidation.Entities:
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Year: 2014 PMID: 25220291 DOI: 10.1016/j.stem.2014.08.003
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633