Epigenetic dynamics of stem cells and cell lineage commitment: digging Waddington's canal

被引:341
|
作者
Hemberger, Myriam [1 ]
Dean, Wendy
Reik, Wolf
机构
[1] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge CB22 3AT, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
PRIMORDIAL GERM-CELLS; HISTONE ARGININE METHYLATION; EMBRYONIC STEM; DNA METHYLATION; TRANSCRIPTIONAL REGULATION; MOUSE EMBRYO; DEVELOPMENTAL REGULATORS; LYSINE METHYLATION; GENE-REGULATION; SELF-RENEWAL;
D O I
10.1038/nrm2727
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells of the early mammalian embryo, including pluripotent embryonic stem (ES) cells and primordial germ cells (PGCs), are epigenetically dynamic and heterogeneous. During early development, this heterogeneity of epigenetic states is associated with stochastic expression of lineage-determining transcription factors that establish an intimate crosstalk with epigenetic modifiers. Lineage-specific epigenetic modification of crucial transcription factor loci (for example, methylation of the Elf5 promoter) leads to the restriction of transcriptional circuits and the fixation of lineage fate. The intersection of major epigenetic reprogramming and programming events in the early embryo creates plasticity followed by commitment to the principal cell lineages of the early conceptus.
引用
收藏
页码:526 / 537
页数:12
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