GATA-4: FOG interactions regulate gastric epithelial development in the mouse

被引:23
作者
Jacobsen, CM
Mannisto, S
Porter-Tinge, S
Genova, E
Parviainen, H
Heikinheimo, M
Adameyko, II
Tevosian, SG
Wilson, DB
机构
[1] Washington Univ, St Louis Childrens Hosp, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[3] Univ Helsinki, Childrens Hosp, Biomedicum Helsinki, Program Dev & Reprod Biol, Helsinki, Finland
[4] Tampere Univ, Pediat Res Ctr, FIN-33101 Tampere, Finland
[5] Univ Hosp, FIN-33101 Tampere, Finland
[6] Dartmouth Coll Sch Med, Dept Genet, Hanover, NH USA
关键词
stomach; transcription factor; gene expression; foregut;
D O I
10.1002/dvdy.20552
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Transcription factor GATA-4 is a key participant in cytodifferentiation of the mouse hindstomach. Here we show that GATA-4 cooperates with a Friend-of-GATA (FOG) cofactor to direct gene expression in this segment of gut. Immunohistochemical staining revealed that GATA-4 and FOG-1 are co-expressed in hindstomach epithelial cells from embryonic days (E) 11.5 to 18.5. The other member of the mammalian FOG family, FOG-2, was not detected in gastric epithelium. To show that GATA-4:FOG interactions influence stomach development, we analyzed Gata4(ki/ki) mice, which express a mutant GATA-4 that cannot bind FOG cofactors. Sonic Hedgehog, an endoderm-derived signaling molecule normally down-regulated in the distal stomach, was over-expressed in hindstomach epithelium of E11.5 Gata4(ki/ki) mice, and there was a concomitant decrease in fibroblast growth factor-10 in adjacent mesenchyme. We conclude that functional interaction between GATA-4 and a member of the FOG family, presumably FOG-1, is required for proper epithelial-mesenchymal signaling in the developing stomach.
引用
收藏
页码:355 / 362
页数:8
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