| Literature DB >> 29967139 |
Ken-Ichiro Abe1, Satoshi Funaya1, Dai Tsukioka1, Machika Kawamura1, Yutaka Suzuki2, Masataka G Suzuki1, Richard M Schultz3,4, Fugaku Aoki5.
Abstract
In mice, transcription initiates at the mid-one-cell stage and transcriptional activity dramatically increases during the two-cell stage, a process called zygotic gene activation (ZGA). Associated with ZGA is a marked change in the pattern of gene expression that occurs after the second round of DNA replication. To distinguish ZGA before and after the second-round DNA replication, the former and latter are called minor and major ZGA, respectively. Although major ZGA are required for development beyond the two-cell stage, the function of minor ZGA is not well understood. Transiently inhibiting minor ZGA with 5, 6-dichloro-1-β-d-ribofuranosyl-benzimidazole (DRB) resulted in the majority of embryos arresting at the two-cell stage and retention of the H3K4me3 mark that normally decreases. After release from DRB, at which time major ZGA normally occurred, transcription initiated with characteristics of minor ZGA but not major ZGA, although degradation of maternal mRNA normally occurred. Thus, ZGA occurs sequentially starting with minor ZGA that is critical for the maternal-to-zygotic transition.Entities:
Keywords: gene expression; maternal-to-zygotic transition; minor zygotic gene activation; preimplantation mouse embryo
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Year: 2018 PMID: 29967139 PMCID: PMC6055165 DOI: 10.1073/pnas.1804309115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205