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A more recent version of this article appeared on April 27, 2001
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Papers In Press, published online ahead of print January 30, 2001
J. Biol. Chem, 10.1074/jbc.M010534200
Submitted on November 21, 2000
Revised on January 29, 2001
Accepted on January 29, 2001

Aberrant expression of human mucin gene MUC5B in gastric carcinoma and gastric cancer cells. Identification and regulation of a distal promoter

Michaël Perrais, Pascal Pigny, Marie-Pierre Buisine, Nicole Porchet, Jean-Pierre Aubert, and Isabelle Van Seuningen-Lempire

Unité INSERM 377, Lille cedex 59045

Corresponding Author: vanseuni{at}lille.inserm.fr

In gastric cancer, altered expression of MUC1, MUC2, MUC5AC and MUC6 mucin genes has already been described. We show in this report, by the means of in situ hybridization, RT-PCR and transfection assays that MUC5B is also abnormally expressed in gastric carcinomatous tissues and cell lines. We thus undertook to elucidate the molecular mechanisms that regulate the transcription of MUC5B in gastric cancer cells. To this end, high-expressing (KATO-III) and low-expressing (AGS) gastric cancer cell lines were chosen to study human mucin gene MUC5B expression and promoter activity. Sequencing of the promoter region revealed a distal TATA box located 1 kilobase upstream of the proximal TATA box. Functional activity of the promoter was addressed by using deletion mutants covering 2044 nucleotides upstream of the MUC5B transcription start site. We identified a distal promoter 10 times more active than the proximal promoter in KATO-III cells. In AGS cells, both promoters, much less active, showed the same range of activity. Binding assays allowed us to show that the transcription factor ATF-1 binds to a cis-element present in the distal promoter. Sp1, which binds to both promoters specifically transactivates the proximal promoter. Treatment of transfected cells with PMA, cholera toxin A subunit, and calcium ionophore A23187 showed that only PMA led to a substantial activation of the distal promoter. MUC5B 5'-flanking region having a high GC content, influence of methylation on the MUC5B expression was assessed. Our results indicate that repression of MUC5B expression visualized in AGS cells is due in part to the presence of numerous methylated cytosine residues throughout the 5'-flanking region. Altogether these results demonstrate that MUC5B expression in gastric cancer cells is governed by a highly active distal promoter that is up-regulated by PKC and that repression is under the influence of methylation.


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