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Epigenetic Control of Cell Potency and Fate Determination during Mammalian Gastrulation
被引:1
|作者:
Sullivan, Adrienne E. E.
[1
,2
,3
]
机构:
[1] Francis Crick Inst, Quantitat Stem Cell Biol Lab, London NW1 1AT, England
[2] Univ Adelaide, Fac Hlth & Med Sci, Adelaide Ctr Epigenet, Sch Biomed, Adelaide 5000, Australia
[3] Univ Adelaide, South Australian immunoGEN Canc Inst SAiGENCI, Fac Hlth & Med Sci, Adelaide 5000, Australia
来源:
关键词:
embryonic stem cells;
epigenetic remodelling;
lineage specification;
embryonic development;
gene regulation;
RNA-POLYMERASE-II;
DNA METHYLATION;
CHROMATIN-STRUCTURE;
SELF-RENEWAL;
HUMAN ES;
DIFFERENTIATION;
TRANSCRIPTION;
COMPLEX;
MAINTENANCE;
ENHANCERS;
D O I:
10.3390/genes14061143
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Pluripotent embryonic stem cells have a unique and characteristic epigenetic profile, which is critical for differentiation to all embryonic germ lineages. When stem cells exit the pluripotent state and commit to lineage-specific identities during the process of gastrulation in early embryogenesis, extensive epigenetic remodelling mediates both the switch in cellular programme and the loss of potential to adopt alternative lineage programmes. However, it remains to be understood how the stem cell epigenetic profile encodes pluripotency, or how dynamic epigenetic regulation helps to direct cell fate specification. Recent advances in stem cell culture techniques, cellular reprogramming, and single-cell technologies that can quantitatively profile epigenetic marks have led to significant insights into these questions, which are important for understanding both embryonic development and cell fate engineering. This review provides an overview of key concepts and highlights exciting new advances in the field.
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页数:16
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