The emergence of genome architecture and zygotic genome activation

被引:30
作者
Vallot, Antoine [1 ]
Tachibana, Kikue [1 ,2 ]
机构
[1] Austrian Acad Sci, Inst Mol Biotechnol, Vienna Bioctr VBC, Dr Bohr Gasse 3, A-1030 Vienna, Austria
[2] Max Planck Inst Biochem, Dept Totipotency, Klopferspitz 18, D-82152 Martinsried, Germany
基金
欧洲研究理事会; 奥地利科学基金会;
关键词
Chromatin structure; Cohesin; Zygotic genome activation; ZGA; Reprogramming; Zygote; Hi-C; Totipotency; Pioneer transcription factor; TAD; CTCF; CHROMATIN ARCHITECTURE; TRANSCRIPTION FACTORS; GENE-EXPRESSION; KEY ACTIVATOR; HUMAN COHESIN; ORGANIZATION; DOMAINS; CTCF; ZELDA; DNA;
D O I
10.1016/j.ceb.2020.02.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fusion of two transcriptionally silent gametes, egg and sperm, generates a totipotent zygote that activates zygotic transcription to support further development. Although the molecular details of zygotic genome activation (ZGA) are not well understood in most species, an emerging concept is that one or more pioneer transcription factors trigger zygotic transcription. Concomitantly, extensive changes in 3D chromatin organization occur during development. In this review, we discuss recent advances in understanding when and how genome architecture emerges in early metazoan embryos, how the zygotic genome is activated, and how these events might be coordinated. We also highlight some of the unknowns that may be critical to address in the future.
引用
收藏
页码:50 / 57
页数:8
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