| Literature DB >> 27843122 |
Hirotaka Hamada1, Hiroaki Okae2, Hidehiro Toh3, Hatsune Chiba1, Hitoshi Hiura1, Kenjiro Shirane3, Tetsuya Sato4, Mikita Suyama4, Nobuo Yaegashi5, Hiroyuki Sasaki3, Takahiro Arima6.
Abstract
DNA methylation is globally reprogrammed after fertilization, and as a result, the parental genomes have similar DNA-methylation profiles after implantation except at the germline differentially methylated regions (gDMRs). We and others have previously shown that human blastocysts might contain thousands of transient maternally methylated gDMRs (transient mDMRs), whose maternal methylation is lost in embryonic tissues after implantation. In this study, we performed genome-wide allelic DNA methylation analyses of purified trophoblast cells from human placentas and, surprisingly, found that more than one-quarter of the transient-in-embryo mDMRs maintained their maternally biased DNA methylation. RNA-sequencing-based allelic expression analyses revealed that some of the placenta-specific mDMRs were associated with expression of imprinted genes (e.g., TIGAR, SLC4A7, PROSER2-AS1, and KLHDC10), and three imprinted gene clusters were identified. This approach also identified some X-linked gDMRs. Comparisons of the data with those from other mammals revealed that genomic imprinting in the placenta is highly variable. These findings highlight the incomplete erasure of germline DNA methylation in the human placenta; understanding this erasure is important for understanding normal placental development and the pathogenesis of developmental disorders with imprinting effects.Entities:
Keywords: DNA methylation; RNA sequencing; X-chromosome inactivation; genomic imprinting; germline differentially methylated region; human placenta; whole-genome bisulfite sequencing
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Year: 2016 PMID: 27843122 PMCID: PMC5097938 DOI: 10.1016/j.ajhg.2016.08.021
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025