Transcriptional activation of the MUC2 gene by p53

被引:49
作者
Ookawa, K
Kudo, T
Aizawa, S
Saito, H
Tsuchida, S
机构
[1] Hirosaki Univ, Sch Med, Dept Biochem 2, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ, Sch Med, Dept Internal Med, Hirosaki, Aomori 0368562, Japan
[3] Hirosaki Univ, Ctr Educ & Res Lifelong Learning, Hirosaki, Aomori 0368560, Japan
关键词
D O I
10.1074/jbc.M207986200
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
MUC2 is one of the major components of mucins that provide a protective barrier between epithelial surfaces and the gut lumen. We investigated possible alterations of MUC2 gene expression by p53 and p21(Sdi1/Waf1/Cip1) in a human colon cancer cell line, DLD-1, establishing subclones in which a tetracycline-regulatable promoter controls exogenous p53 and p21. expression. MUC2 mRNA more significantly increased in response to p53 than to p21. Unexpectedly, MUC2 expression was also induced in human osteosarcoma cells, U-2OS and Saos-2, by exogenous p53. We next performed a reporter assay to test the direct regulation of MUC2 gene expression by p53. Deletion and mutagenesis of the MUC2 promoter region showed that it contains two sites for transactivation by p53. Furthermore, an electrophoretic mobility shift assay indicated that p53 binds to those elements. We analyzed MUC2 expression in other cell types possessing a functional p53 after exposure to various forms of stress. In MCF7 breast cancer and A427 lung cancer cells, MUC2 expression was increased along with the endogenous p53 level by actinomycin D, UVC, and x-ray, but not in RERF-LC-MS lung cancer cells carrying a mutated p53. These results suggest that p53 directly activates the MUC2 gene in many cell types.
引用
收藏
页码:48270 / 48275
页数:6
相关论文
共 47 条
[1]   Phenotypic alterations of small cell lung carcinoma induced by different levels of wild-type p53 expression [J].
Adachi, J ;
Ookawa, K ;
Kohno, T ;
Tomizawa, Y ;
Tsuchida, S ;
Yokota, J .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (02) :148-155
[2]   The MUC2 gene product: a human intestinal mucin [J].
Allen, A ;
Hutton, DA ;
Pearson, JP .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1998, 30 (07) :797-801
[3]  
Aslam F, 2001, CANCER RES, V61, P570
[4]  
Baldus SE, 1998, INT J CANCER, V79, P133, DOI 10.1002/(SICI)1097-0215(19980417)79:2<133::AID-IJC6>3.0.CO
[5]  
2-U
[6]   EXPRESSION OF MUC2-MUCIN IN COLORECTAL ADENOMAS AND CARCINOMAS OF DIFFERENT HISTOLOGICAL TYPES [J].
BLANK, M ;
KLUSSMANN, E ;
KRUGERKRASAGAKES, S ;
SCHMITTGRAFF, A ;
STOLTE, M ;
BORNHOEFT, G ;
STEIN, H ;
XING, PX ;
MCKENZIE, IFC ;
VERSTIJNEN, CPHJ ;
RIECKEN, EO ;
HANSKI, C .
INTERNATIONAL JOURNAL OF CANCER, 1994, 59 (03) :301-306
[7]  
CAMPO E, 1991, CANCER RES, V51, P4436
[8]  
CASEY G, 1991, ONCOGENE, V6, P1791
[9]   P53 FUNCTIONS AS A CELL-CYCLE CONTROL PROTEIN IN OSTEOSARCOMAS [J].
DILLER, L ;
KASSEL, J ;
NELSON, CE ;
GRYKA, MA ;
LITWAK, G ;
GEBHARDT, M ;
BRESSAC, B ;
OZTURK, M ;
BAKER, SJ ;
VOGELSTEIN, B ;
FRIEND, SH .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (11) :5772-5781
[10]   DEFINITION OF A CONSENSUS BINDING-SITE FOR P53 [J].
ELDEIRY, WS ;
KERN, SE ;
PIETENPOL, JA ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE GENETICS, 1992, 1 (01) :45-49