| Literature DB >> 29255258 |
Ping Zhu1,2,3,4, Hongshan Guo1,2,5, Yixin Ren1,6, Yu Hou1,2, Ji Dong1,2, Rong Li1,6, Ying Lian1,6, Xiaoying Fan1,2, Boqiang Hu1,2, Yun Gao1,2, Xiaoye Wang1,6, Yuan Wei1,6, Ping Liu1,6, Jie Yan1,6, Xiulian Ren1,6, Peng Yuan1,6, Yifeng Yuan1,6, Zhiqiang Yan1,6, Lu Wen1,2, Liying Yan7,8,9,10, Jie Qiao11,12,13,14,15,16, Fuchou Tang17,18,19,20,21.
Abstract
DNA methylation is a crucial layer of epigenetic regulation during mammalian embryonic development 1-3 . Although the DNA methylome of early human embryos has been analyzed 4-6 , some of the key features have not been addressed thus far. Here we performed single-cell DNA methylome sequencing for human preimplantation embryos and found that tens of thousands of genomic loci exhibited de novo DNA methylation. This finding indicates that genome-wide DNA methylation reprogramming during preimplantation development is a dynamic balance between strong global demethylation and drastic focused remethylation. Furthermore, demethylation of the paternal genome is much faster and thorough than that of the maternal genome. From the two-cell to the postimplantation stage, methylation of the paternal genome is consistently lower than that of the maternal genome. We also show that the genetic lineage of early blastomeres can be traced by DNA methylation analysis. Our work paves the way for deciphering the secrets of DNA methylation reprogramming in early human embryos.Entities:
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Year: 2017 PMID: 29255258 DOI: 10.1038/s41588-017-0007-6
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330