Epigenetic programming and reprogramming during development

被引:316
作者
Cantone, Irene [1 ]
Fisher, Amanda G. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Lymphocyte Dev Grp, Med Res Council Clin Sci Ctr, London, England
基金
英国医学研究理事会;
关键词
PLURIPOTENT STEM-CELLS; ACTIVE DNA DEMETHYLATION; HISTONE H3; TRANSCRIPTIONAL ACTIVITY; PATERNAL GENOME; EFFECT GENE; GERM-CELLS; METHYLATION; CHROMATIN; REPLICATION;
D O I
10.1038/nsmb.2489
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell identity is determined by specific gene expression patterns that are conveyed by interactions between transcription factors and DNA in the context of chromatin. In development, epigenetic modifiers are thought to stabilize gene expression and ensure that patterns of DNA methylation and histone modification are reinstated in cells as they divide. Global erasure of epigenetic marks occurs naturally at two stages in the mammalian life cycle, but it can also be artificially engineered using a variety of reprogramming strategies. Here we review some of the recent advances in understanding how epigenetic remodeling contributes to conversion of cell fate in vivo and in vitro. We summarize current models of epigenetic erasure and discuss the various enzymes and mechanisms that may operate in cellular reprogramming.
引用
收藏
页码:282 / 289
页数:8
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