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PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells.

María Inés Pérez Millán | Michelle L Brinkmeier | Amanda H Mortensen | Sally A Camper
eLife | 2016

Mutations in PROP1 are the most common cause of hypopituitarism in humans; therefore, unraveling its mechanism of action is highly relevant from a therapeutic perspective. Our current understanding of the role of PROP1 in the pituitary gland is limited to the repression and activation of the pituitary transcription factor genes Hesx1 and Pou1f1, respectively. To elucidate the comprehensive PROP1-dependent gene regulatory network, we conducted genome-wide analysis of PROP1 DNA binding and effects on gene expression in mutant mice, mouse isolated stem cells and engineered mouse cell lines. We determined that PROP1 is essential for stimulating stem cells to undergo an epithelial to mesenchymal transition-like process necessary for cell migration and differentiation. Genomic profiling reveals that PROP1 binds to genes expressed in epithelial cells like Claudin 23, and to EMT inducer genes like Zeb2, Notch2 and Gli2. Zeb2 activation appears to be a key step in the EMT process. Our findings identify PROP1 as a central transcriptional component of pituitary stem cell differentiation.

Pubmed ID: 27351100

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: P30 CA046592
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK034933
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD030428
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD034283

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