Epigenetic regulation of cell fate transition: learning from early embryo development and somatic cell reprogramming†

被引:8
|
作者
Chen, Chuan [1 ]
Gao, Yawei [1 ]
Liu, Wenqiang [2 ]
Gao, Shaorong [1 ,2 ]
机构
[1] Tongji Univ, Shanghai East Hosp, Frontier Sci Ctr Stem Cell Res,Inst Regenerat Med, Sch Life Sci & Technol,Shanghai Key Lab Signaling, Shanghai, Peoples R China
[2] Tongji Univ, Frontier Sci Ctr Stem Cell Res, Clin & Translat Res Ctr,Shanghai Key Lab Signalin, Sch Life Sci & Technol,Shanghai Matern & Infant H, Shanghai, Peoples R China
关键词
epigenetic dynamics; embryo development; reprogramming; transcriptome transition; regulatory network; MOUSE EARLY EMBRYOS; DNA METHYLATION; ENDOGENOUS RETROVIRUSES; MAMMALIAN DEVELOPMENT; HISTONE ACETYLATION; IPS CELLS; CHROMATIN; OOCYTES; H3K4ME3; IDENTIFICATION;
D O I
10.1093/biolre/ioac087
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epigenetic regulations play a central role in governing the embryo development and somatic cell reprogramming. Taking advantage of recent advances in low-input sequencing techniques, researchers have uncovered a comprehensive view of the epigenetic landscape during rapid transcriptome transitions involved in the cell fate commitment. The well-organized epigenetic reprogramming also highlights the essential roles of specific epigenetic regulators to support efficient regulation of transcription activity and chromatin remodeling. This review briefly introduces the recent progress in the molecular dynamics and regulation mechanisms implicated in mouse early embryo development and somatic cell reprograming, as well as the multi-omics regulatory mechanisms of totipotency mediated by several key factors, which provide valuable resources for further investigations on the complicated regulatory network in essential biological events.
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页码:183 / 195
页数:13
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