Epigenetic restriction of embryonic cell lineage fate by methylation of Elf5

被引:278
作者
Ng, Ray Kit [1 ,2 ]
Dean, Wendy [1 ]
Dawson, Claire [1 ]
Lucifero, Diana [1 ]
Madeja, Zofia [1 ,2 ]
Reik, Wolf [1 ,2 ]
Hemberger, Myriam [1 ,2 ]
机构
[1] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge CB22 3AT, England
[2] Univ Cambridge, Ctr Trophoblast Res, Cambridge CB2 3EG, 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
D O I
10.1038/ncb1786
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mouse ES cells can differentiate into all three germ layers of the embryo but are generally excluded from the trophoblast lineage. Here we show that ES cells deficient in DNA methylation can differentiate efficiently into trophoblast derivatives. In a genome-wide screen we identified the transcription factor Elf5 as methylated and repressed in ES cells, and hypomethylated and expressed in TS and methylation-deficient ES cells. Elf5 creates a positive-feedback loop with the TS cell determinants Cdx2 and Eomes that is restricted to the trophoblast lineage by epigenetic regulation of Elf5. Importantly, the late-acting function of Elf5 allows initial plasticity and regulation in the early blastocyst. Thus, Elf5 functions as a gatekeeper, downstream of initial lineage determination, to reinforce commitment to the trophoblast lineage or to abort this pathway in epiblast cells. This epigenetic restriction of cell lineage fate provides a molecular mechanism for Waddington's concept of canalization of developmental pathways.
引用
收藏
页码:1280 / U68
页数:16
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