POU homeodomain protein OCT1 is implicated in the expression of the caudal-related homeobox gene Cdx-2

被引:33
作者
Jin, TR
Li, HQ
机构
[1] Univ Toronto, Univ Hlth Network, Toronto Gen Res Inst, Div Cell & Mol Biol, Toronto, ON M5G 2M1, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M1, Canada
[3] Univ Toronto, Dept Med, Toronto, ON M5G 2M1, Canada
关键词
D O I
10.1074/jbc.M008277200
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 caudal homeobox gene Cdx-2 is a transcriptional activator for approximately a dozen genes specifically expressed in pancreatic islets and intestinal cells. It is also involved in preventing the development of colorectal tumors. Studies using "knockout" approaches demonstrated that Cdx-2 is haplo-insufficient in certain tissues including the intestines but not the pancreatic islets, The mechanisms, especially transcription factors, which regulate Cdx-2 expression, are virtually unknown. We found previously that Cdx-2 expression could be autoregulated in a cell type-specific manner. In this study, we located an octamer (OCT) binding site within the mouse Cdx-2 gene promoter, This site, designated as Cdx-2(P)OCT, is involved in the expression of the Cdx-2 promoter. Both pancreatic and intestinal cell lines were found to express a number of POU (OCT binding) homeodomain proteins examined by electrophoretic mobility shift assay. However, it appears that Cdx-2(P)OCT interacts only with OCT1 in the nuclear extracts of the intestinal cell lines examined, although it interacts with OCT1 and at least two other POU proteins that are to be identified in the pancreatic InR1-G9 cell nuclear extract. Co-transfecting OCT1 cDNA but not five other POU gene cDNAs activates the Cdx-2 promoter in the pancreatic InR1-G9 and the intestinal Caco-2 cell lines. In contrast, Cdx-2(P)OCT cannot act as an enhancer element if it is fused to a thymidine kinase promoter. Furthermore, Cdx-2(P)OCT-thymidine kinase fusion promoters cannot be activated by OCT1 co-transfection, Cell type-specific expression, cell type-specific binding affinity of POU proteins to the cis-element Cdx-2(P)OCT, and the DNA content-dependent activation of Cdx-2 promoter via Cdx-2POCT by OCT1 suggest that POU proteins play important and complicated roles in modulating Cdx-2 expression in cell type-specific manners.
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页码:14752 / 14758
页数:7
相关论文
共 48 条
[21]  
JAMES R, 1991, J BIOL CHEM, V266, P3246
[22]  
JAMES R, 1994, J BIOL CHEM, V269, P15229
[23]   THE PROGLUCAGON GENE UPSTREAM ENHANCER CONTAINS POSITIVE AND NEGATIVE DOMAINS IMPORTANT FOR TISSUE-SPECIFIC PROGLUCAGON GENE-TRANSCRIPTION [J].
JIN, T ;
DRUCKER, DJ .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (10) :1306-1320
[24]  
Jin TR, 1999, INT J CANCER, V81, P104, DOI 10.1002/(SICI)1097-0215(19990331)81:1<104::AID-IJC18>3.0.CO
[25]  
2-Q
[26]  
Jin TR, 1996, MOL CELL BIOL, V16, P19
[27]   The caudal-related homeodomain protein Cdx-2/3 regulates glucagon gene expression in islet cells [J].
Laser, B ;
Meda, P ;
Constant, I ;
Philippe, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) :28984-28994
[28]   OCT-1 AND OCT-2 POTENTIATE FUNCTIONAL INTERACTIONS OF A TRANSCRIPTION FACTOR WITH THE PROXIMAL SEQUENCE ELEMENT OF SMALL NUCLEAR-RNA GENES [J].
MURPHY, S ;
YOON, JB ;
GERSTER, T ;
ROEDER, RG .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (07) :3247-3261
[29]   A single serine residue at position 375 of VP16 is critical for complex assembly with Oct-1 and HCF and is a target of phosphorylation by casein kinase II [J].
OReilly, D ;
Hanscombe, O ;
OHare, P .
EMBO JOURNAL, 1997, 16 (09) :2420-2430
[30]   Selective binding of steroid hormone receptors to octamer transcription factors determines transcriptional synergism at the mouse mammary tumor virus promoter [J].
Préfontaine, GG ;
Walther, R ;
Giffin, W ;
Lemieux, ME ;
Pope, L ;
Haché, RJG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26713-26719