TCF and SOX proteins belong to the high mobility group box transcription factor family. Whereas TCFs, the transcriptional effectors of the Wnt pathway, have been widely implicated in the development, homeostasis and disease of the intestine epithelium, little is known about the function of the SOX proteins in this tissue. Here, we identified SOX9 in a SOX expression screening in the mouse fetal intestine. We report that the SOX9 protein is expressed in the intestinal epithelium in a pattern characteristic of Wnt targets. We provide in vitro and in vivo evidence that a bipartite β-catenin/TCF4 transcription factor, the effector of the Wnt signaling pathway, is required for SOX9 expression in epithelial cells. Finally, in colon epithelium-derived cells, SOX9 transcriptionally represses the CDX2 and MUC2 genes, normally expressed in the mature villus cells of the intestinal epithelium, and may therefore contribute to the Wnt-dependent maintenance of a progenitor cell phenotype.
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5 July 2004
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July 06 2004
SOX9 is an intestine crypt transcription factor, is regulated by the Wnt pathway, and represses the CDX2 and MUC2 genes
Philippe Blache,
Philippe Blache
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
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Marc van de Wetering,
Marc van de Wetering
2Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, Netherlands
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Isabelle Duluc,
Isabelle Duluc
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
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Claire Domon,
Claire Domon
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
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Philippe Berta,
Philippe Berta
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
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Jean-Noël Freund,
Jean-Noël Freund
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
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Hans Clevers,
Hans Clevers
2Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, Netherlands
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Philippe Jay
Philippe Jay
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
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Philippe Blache
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
Marc van de Wetering
2Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, Netherlands
Isabelle Duluc
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
Claire Domon
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
Philippe Berta
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
Jean-Noël Freund
3Institut National de la Santé et de la Recherche Médicale (INSERM) U381, F-67200 Strasbourg, France
Hans Clevers
2Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, Netherlands
Philippe Jay
1Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS) UPR1142, 34396 Montpellier, Cedex 5, France
Address correspondence to Philippe Jay, Institut de Génétique Humaine, CNRS UPR1142, 141 rue de la Cardonille, 34396 Montpellier, Cedex 5, France. Tel.: 33-499-61-99-40. Fax: 33-499-61-99-01. email: [email protected]
The online version of this article contains supplemental material.
Abbreviations used in this paper: CD, campomelic dysplasia; cyt-E-cadherin, cytoplasmic domain of E-cadherin.
Received:
November 05 2003
Accepted:
May 29 2004
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2004
J Cell Biol (2004) 166 (1): 37–47.
Article history
Received:
November 05 2003
Accepted:
May 29 2004
Citation
Philippe Blache, Marc van de Wetering, Isabelle Duluc, Claire Domon, Philippe Berta, Jean-Noël Freund, Hans Clevers, Philippe Jay; SOX9 is an intestine crypt transcription factor, is regulated by the Wnt pathway, and represses the CDX2 and MUC2 genes . J Cell Biol 5 July 2004; 166 (1): 37–47. doi: https://doi.org/10.1083/jcb.200311021
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