| Literature DB >> 29414683 |
Jin Zhang1, Jing Zhao2, Perrine Dahan3, Vivian Lu4, Cheng Zhang5, Hu Li5, Michael A Teitell6.
Abstract
Emerging and seminal studies have shown that cell metabolism influences gene expression by modifying the epigenome, which can regulate stem cell pluripotency, differentiation, and somatic cell reprogramming. Core pluripotency factors and developmental regulators reciprocally control the expression of key metabolism genes and their encoded pathways. Recent technological advances enabling sensitive detection methods during early mammalian development revealed the state-specific and context-dependent coordination of signal transduction, histone modifications, and gene expression in developing, resting, and malnourished embryos. Here, we discuss metabolism as a potential driver of earliest cell fate through its influence on the epigenome and gene expression in embryos and their in vitro surrogate pluripotent stem cells.Entities:
Mesh:
Year: 2018 PMID: 29414683 DOI: 10.1016/j.cmet.2018.01.008
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287