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

被引:109
作者
Guo, Y
Costa, R
Ramsey, H
Starnes, T
Vance, G
Robertson, K
Kelley, M
Reinbold, R
Scholer, H
Hromas, R
机构
[1] Indiana Univ, Med Ctr, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ, Med Ctr, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[3] Univ Illinois, Coll Med, Dept Mol Genet, Chicago, IL 60607 USA
[4] Indiana Univ, Med Ctr, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[5] Indiana Univ, Med Ctr, James Whitcomb Riley Hosp Children, Dept Pediat, Indianapolis, IN 46202 USA
[6] Indiana Univ, Med Ctr, James Whitcomb Riley Hosp Children, Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[7] Univ Penn, New Bolton Ctr, Sch Vet Med, Ctr Anim Transgenesis & Germ Cell Res, Kennett Sq, PA 19348 USA
关键词
D O I
10.1073/pnas.062041099
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. Cortransfection of Oct-4 and FoxD3 expression vectors activated the osteopontin enhancer, which is expressed in totipotent embryonic stem cells. FoxA1 and FoxA2 (previously HNF-3alpha and HNF-3beta) 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.
引用
收藏
页码:3663 / 3667
页数:5
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