The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression

  1. Ying Guo*,
  2. Robert Costa,
  3. Heather Ramsey*,
  4. Trevor Starnes*,
  5. Gail Vance,
  6. Kent Robertson§,
  7. Mark Kelley§,
  8. Rolland Reinbold,
  9. Hans Scholer, and
  10. Robert Hromas*,
  1. *Department of Medicine and The Walther Oncology Center, R4-202, 1044 West Walnut Street, Indiana University Medical Center, Indianapolis, IN 46202; Department of Molecular Genetics, University of Illinois College of Medicine, 900 South Ashland Avenue, Chicago, IL 60607-7170; Department of Medical and Molecular Genetics, IB 264, 975 West Walnut Street, Indiana University Medical Center, Indianapolis, IN 46202; §Department of Pediatrics and Wells Center for Pediatric Research, James Whitcomb Riley Hospital for Children, 702 Barnhill Drive, Indiana University Medical Center, Indianapolis, IN 46202; and Center for Animal Transgenesis and Germ Cell Research, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19348
  1. Communicated by Lawrence H. Einhorn, Indiana University Cancer Center, Indianapolis, IN (received for review October 1, 2001)

Abstract

The POU homeodomain protein Oct-4 and the Forkhead Box protein FoxD3 (previously Genesis) are transcriptional regulators expressed in embryonic stem cells. Down-regulation of Oct-4 during gastrulation is essential for proper endoderm development. After gastrulation, FoxD3 is generally down-regulated during early endoderm formation, although it specifically remains expressed in the embryonic neural crest. In these studies, we have found that Oct-4 and FoxD3 can bind to identical regulatory DNA sequences. In addition, Oct-4 physically interacted with the FoxD3 DNA-binding domain. Cotransfection of Oct-4 and FoxD3 expression vectors activated the osteopontin enhancer, which is expressed in totipotent embryonic stem cells. FoxA1 and FoxA2 (previously HNF-3α and HNF-3β) are Forkhead Box transcription factors that participate in liver and lung formation from foregut endoderm. Although FoxD3 activated the FoxA1 and FoxA2 promoters, Oct-4 inhibited FoxD3 activation of the FoxA1 and FoxA2 endodermal promoters. These data indicate that Oct-4 functions as a corepressor of FoxD3 to provide embryonic lineage-specific transcriptional regulatory activity to maintain appropriate developmental timing.

Footnotes

  • To whom reprint requests should be addressed. E-mail: rhromas{at}iupui.edu.

  • Abbreviations:
    ES,
    embryonic stem;
    GST,
    glutathione S-transferase;
    EMSA,
    electrophoretic mobility-shift assay
« Previous | Next Article »Table of Contents