4.8 Article

Core transcriptional regulatory circuitry in human embryonic stem cells

Journal

CELL
Volume 122, Issue 6, Pages 947-956

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2005.08.020

Keywords

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Funding

  1. NCI NIH HHS [CA094664, F32 CA094664] Funding Source: Medline
  2. NHGRI NIH HHS [R01 HG002668-02, R01 HG002668, HG002668] Funding Source: Medline
  3. NIGMS NIH HHS [R01 GM069400, GM068273, GM069400, F32 GM068273] Funding Source: Medline

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The transcription factors OCT4, SOX2, and NANOG have essential roles in early development and are required for the propagation of undifferentiated embryonic stem (ES) cells in culture. To gain insights into transcriptional regulation of human ES cells, we have identified OCT4, SOX2, and NANOG target genes using genome-scale location analysis. We found, surprisingly, that OCT4, SOX2, and NANOG co-occupy a substantial portion of their target genes. These target genes frequently encode transcription factors, many of which are developmentally important homeodomain proteins. Our data also indicate that OCT4, SOX2, and NANOG collaborate to form regulatory circuitry consisting of autoregulatory and feedforward loops. These results provide new insights into the transcriptional regulation of stem cells and reveal how OCT4, SOX2, and NANOG contribute to pluripotency and self-renewal.

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