Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells
- PMID: 10742100
- DOI: 10.1038/74199
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells
Abstract
Cell fate during development is defined by transcription factors that act as molecular switches to activate or repress specific gene expression programmes. The POU transcription factor Oct-3/4 (encoded by Pou5f1) is a candidate regulator in pluripotent and germline cells and is essential for the initial formation of a pluripotent founder cell population in the mammalian embryo. 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 into primitive endoderm and mesoderm. In contrast, repression 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 role 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.
Comment in
-
Oct-4, scene 1: the drama of mouse development.Nat Genet. 2000 Apr;24(4):328-30. doi: 10.1038/74129. Nat Genet. 2000. PMID: 10742086 No abstract available.
Similar articles
-
Oct-3/4 and Sox2 regulate Oct-3/4 gene in embryonic stem cells.J Biol Chem. 2005 Feb 18;280(7):5307-17. doi: 10.1074/jbc.M410015200. Epub 2004 Nov 22. J Biol Chem. 2005. PMID: 15557334
-
Oct-4 knockdown induces similar patterns of endoderm and trophoblast differentiation markers in human and mouse embryonic stem cells.Stem Cells. 2004;22(2):225-35. doi: 10.1634/stemcells.22-2-225. Stem Cells. 2004. PMID: 14990861
-
Small increases in the level of Sox2 trigger the differentiation of mouse embryonic stem cells.Stem Cells. 2008 Apr;26(4):903-11. doi: 10.1634/stemcells.2007-0951. Epub 2008 Jan 31. Stem Cells. 2008. PMID: 18238855
-
Oct-4: gatekeeper in the beginnings of mammalian development.Stem Cells. 2001;19(4):271-8. doi: 10.1634/stemcells.19-4-271. Stem Cells. 2001. PMID: 11463946 Review.
-
Oct-3/4: not just a gatekeeper of pluripotency for embryonic stem cell, a cell fate instructor through a gene dosage effect.Cell Cycle. 2007 Jan 1;6(1):8-10. doi: 10.4161/cc.6.1.3633. Epub 2007 Jan 29. Cell Cycle. 2007. PMID: 17245123 Review.
Cited by
-
CD133 expression predicts lung metastasis and poor prognosis in osteosarcoma patients: A clinical and experimental study.Exp Ther Med. 2012 Sep;4(3):435-441. doi: 10.3892/etm.2012.603. Epub 2012 Jun 8. Exp Ther Med. 2012. PMID: 23181114 Free PMC article.
-
Directed Evolution of an Enhanced POU Reprogramming Factor for Cell Fate Engineering.Mol Biol Evol. 2021 Jun 25;38(7):2854-2868. doi: 10.1093/molbev/msab075. Mol Biol Evol. 2021. PMID: 33720298 Free PMC article.
-
The quantitative proteomes of human-induced pluripotent stem cells and embryonic stem cells.Mol Syst Biol. 2011 Nov 22;7:550. doi: 10.1038/msb.2011.84. Mol Syst Biol. 2011. PMID: 22108792 Free PMC article.
-
Optimal ratio of transcription factors for somatic cell reprogramming.J Biol Chem. 2012 Oct 19;287(43):36273-82. doi: 10.1074/jbc.M112.380683. Epub 2012 Sep 6. J Biol Chem. 2012. PMID: 22955270 Free PMC article.
-
Human embryonic stem cells differentiated to lung lineage-specific cells ameliorate pulmonary fibrosis in a xenograft transplant mouse model.PLoS One. 2012;7(3):e33165. doi: 10.1371/journal.pone.0033165. Epub 2012 Mar 28. PLoS One. 2012. PMID: 22470441 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
