Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells

被引:2729
|
作者
Niwa, H
Miyazaki, J
Smith, AG
机构
[1] Univ Edinburgh, Ctr Genome Res, Edinburgh, Midlothian, Scotland
[2] Osaka Univ, Dept Nutr & Physiol Chem, Osaka, Japan
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1038/74199
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cell fate during development is defined by transcription factors that act as molecular switches to activate or repress specific less than twofold increase in expression causes differentiation gene expression programmes. The POU transcription factor into primitive endoderm and mesoderm, In contrast, repression Oct-3/4 (encoded by Pou5f1) is a candidate regulator in pluripotent and germline cells(1-4) and is essential for the initial formation of a pluripotent founder cell population in the mammalian embryo(5). Here we use conditional expression and repression in embryonic stem (ES) cells to determine requirements for Oct-3/4 in the maintenance of developmental potency. Although transcriptional determination has usually been considered as a binary on-off control system, we found that the precise level of Oct-3/4 governs three distinct fates of ES cells, A less than twofold increase in expression causes differentiation of Oct-3/4 induces loss of pluripotency and dedifferentiation to trophectoderm. Thus a critical amount of Oct-3/4 is required to sustain stem-cell self-renewal, and up- or downregulation induce divergent developmental programmes. Our findings establish a pole for Oct-3/4 as a master regulator of pluripotency that controls lineage commitment and illustrate the sophistication of critical transcriptional regulators and the consequent importance of quantitative analyses.
引用
收藏
页码:372 / 376
页数:5
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