The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression
- Ying Guo*,
- Robert Costa†,
- Heather Ramsey*,
- Trevor Starnes*,
- Gail Vance‡,
- Kent Robertson§,
- Mark Kelley§,
- Rolland Reinbold¶,
- Hans Scholer¶, and
- Robert Hromas*,‖
- *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
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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
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↵ ‖ 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
- Copyright © 2002, The National Academy of Sciences





