CEACAM1, a SOX9 direct transcriptional target identified in the colon epithelium

被引:37
作者
Zalzali, H. [2 ,3 ]
Naudin, C. [2 ,3 ]
Bastide, P. [2 ,3 ]
Quittau-Prevostel, C. [2 ,3 ]
Yaghi, C. [4 ]
Poulat, F. [5 ]
Jay, P. [2 ,3 ]
Blache, P. [1 ,2 ,3 ]
机构
[1] Univ Montpellier, CNRS, UMR 5203, Inst Genome Fonct, F-34094 Montpellier 5, France
[2] INSERM, U661, Montpellier, France
[3] Univ Montpellier 1, Montpellier, France
[4] Univ St Joseph Achrafieh, Serv Gastroenterol, CHU Hotel Dieu France, Beirut, Lebanon
[5] Inst Genet Humaine, CNRS, UPR 1142, Montpellier, France
关键词
CEACAM1; colon epithelium; SOX9;
D O I
10.1038/onc.2008.331
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
A deletion of the transcription factor SOX9 gene in the mice intestine affects the morphology of the colon epithelium and leads to hyperplasia. Nevertheless, direct transcriptional targets of SOX9 in this tissue are still unknown. A microarray analysis identified the tumor suppressor carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) as a possible SOX9 target gene and we demonstrate here that SOX9 upregulates CEACAM1 in human colonic cells. Moreover, CEACAM1 expression is reduced in colon of SOX9-deficient mouse, suggesting an important function for SOX9 in the transcriptional activation of the CEACAM1 gene. We further identified SOX9-binding sequences in the human and rat CEACAM1 promoters, and an electrophoretic mobility shift together with a chromatin immunoprecipitation provided an additional evidence of the SOX9 binding to the human promoter. In addition, we established that histone acyl-transferase p300 behaves as an SOX9 coactivator of the rat and human CEACAM1 promoters. These results highlight CEACAM1 as the first direct target of SOX9 identified in the colon epithelium.
引用
收藏
页码:7131 / 7138
页数:8
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