The human mucin MUC4 is transcriptionally regulated by caudal-related homeobox, hepatocyte nuclear factors, forkhead box A, and GATA endodermal transcription factors in epithelial cancer cells

被引:42
作者
Jonckheere, Nicolas
Vincent, Audrey
Perrais, Michael
Ducourouble, Marie-Paule
Korteland-van Male, Anita
Aubert, Jean-Pierre
Pigny, Pascal
Carraway, Kermit L.
Freund, Jean-Noel
Renes, Ingrid B.
Van Seuningen, Isabelle
机构
[1] INSERM, U560, F-59045 Lille, France
[2] Erasmus MC, Dept Pediat, Div Gastroenterol, NL-3015 GE Rotterdam, Netherlands
[3] Erasmus MC, Dept Pediat, Div Nutr, NL-3015 GE Rotterdam, Netherlands
[4] Erasmus MC, Div Neonatol, NL-3015 GE Rotterdam, Netherlands
[5] Sophia Childrens Univ Hosp, NL-3015 GE Rotterdam, Netherlands
[6] Univ Miami, Sch Med, Dept Cell Biol & Anat, Miami, FL 33136 USA
[7] INSERM, U682, F-67200 Strasbourg, France
关键词
D O I
10.1074/jbc.M700905200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human gene MUC4 encodes a large transmembrane mucin that is developmentally regulated and expressed along the undifferfetal development. Immunohistochemical analysis of Muc4 expression inentiated pseudostratified epithelium, as early as 6.5 weeks during developing mouse lung and gastrointestinal tract showed a different spatio-temporal pattern of expression before and after cytodifferentiation. The molecular mechanisms governing MUC4 expression during development are, however, unknown. Hepatocyte nuclear factors (HNF), forkhead box A (FOXA), GATA, and caudal-related homeobox transcription factors (TFs) are known to control cell differentiation of gut endoderm derived-tissues during embryonic development. They also control the expression of cell- and tissue-specific genes and may thus control MUC4 expression. To test this hypothesis, we studied and deciphered the molecular mechanisms responsible for MUC4 transcriptional regulation by these TFs. Experiments using small interfering RNA, cell co-transfection, and site-directed mutagenesis indicated that MUC4 is regulated at the transcriptional level by CDX-1 and -2, HNF-1 alpha and -1 beta, FOXA1/A2, HNF-4 alpha and -4 gamma, and GATA-4, -5, and -6 factors in a cell- specific manner. Binding of TFs was assessed by chromatin immunoprecipitation, and gel-shift assays. Altogether, these results demonstrate that MUC4 is a target gene of endodermal TFs and thus point out an important role for these TFs in regulating MUC4 expression during epithelial differentiation during development, cancer, and repair.
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收藏
页码:22638 / 22650
页数:13
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