PAX8-mediated activation of the wt1 tumor suppressor gene

被引:59
作者
Dehbi, M
Pelletier, J
机构
[1] MCGILL UNIV,DEPT BIOCHEM,MONTREAL,PQ H3G 1Y6,CANADA
[2] MCGILL UNIV,MCGILL CANC CTR,MONTREAL,PQ H3G 1Y6,CANADA
关键词
kidney development; Pax-8; Wilms tumor; wt1;
D O I
10.1002/j.1460-2075.1996.tb00804.x
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 developing renal system has long been exploited to study the regulation of gene expression during mesenchymal-epithelial transitions. Several transcription factors, including WT1 and PAX8, are expressed early in nephrogenesis and play a key role in this process, The expression of PAX8 occurs in the induced mesenchyme of the developing kidney prior to the upregulation of WT1 levels in the same cells. In this report, we assessed whether the Pax-8 gene product resides upstream of wt1 in a common regulatory pathway. Transfection studies, as well as gel-shift assays, indicate that PAX8 transactivates wt1 through elements within a 38 bp conserved motif, present in human and murine promoters, Two PAXS isoforms, generated by alternative splicing at the C-terminus and previously thought to lack transactivation potential, were found to be capable of activating wt1 expression, We also demonstrate that the endogenous wt1 promoter can be upregulated by exogenously supplied PAXS, suggesting that a function of PAXS during mesenchymal-epithelial cell transition in renal development is to induce wt1 gene expression.
引用
收藏
页码:4297 / 4306
页数:10
相关论文
共 63 条
[1]   PAX-5 ENCODES THE TRANSCRIPTION FACTOR BSAP AND IS EXPRESSED IN LYMPHOCYTES-B, THE DEVELOPING CNS, AND ADULT TESTIS [J].
ADAMS, B ;
DORFLER, P ;
AGUZZI, A ;
KOZMIK, Z ;
URBANEK, P ;
MAURERFOGY, I ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1992, 6 (09) :1589-1607
[2]  
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[3]   A NOVEL B-CELL LINEAGE-SPECIFIC TRANSCRIPTION FACTOR PRESENT AT EARLY BUT NOT LATE STAGES OF DIFFERENTIATION [J].
BARBERIS, A ;
WIDENHORN, K ;
VITELLI, L ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1990, 4 (05) :849-859
[4]   REARRANGEMENT OF THE PAX3 PAIRED BOX GENE IN THE PEDIATRIC SOLID TUMOR ALVEOLAR RHABDOMYOSARCOMA [J].
BARR, FG ;
GALILI, N ;
HOLICK, J ;
BIEGEL, JA ;
ROVERA, G ;
EMANUEL, BS .
NATURE GENETICS, 1993, 3 (02) :113-117
[5]  
BECKWITH J B, 1990, Pediatric Pathology, V10, P1
[6]   CONSERVATION OF A LARGE PROTEIN DOMAIN IN THE SEGMENTATION GENE PAIRED AND IN FUNCTIONALLY RELATED GENES OF DROSOPHILA [J].
BOPP, D ;
BURRI, M ;
BAUMGARTNER, S ;
FRIGERIO, G ;
NOLL, M .
CELL, 1986, 47 (06) :1033-1040
[7]   A non-AUG translational initiation event generates novel WT1 isoforms [J].
Bruening, W ;
Pelletier, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :8646-8654
[8]  
Bruening Wendy, 1994, Seminars in Developmental Biology, V5, P333, DOI 10.1006/sedb.1994.1042
[9]   ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS [J].
CALL, KM ;
GLASER, T ;
ITO, CY ;
BUCKLER, AJ ;
PELLETIER, J ;
HABER, DA ;
ROSE, EA ;
KRAL, A ;
YEGER, H ;
LEWIS, WH ;
JONES, C ;
HOUSMAN, DE .
CELL, 1990, 60 (03) :509-520
[10]   THE MOLECULAR-BASIS OF THE UNDULATED PAX-1 MUTATION [J].
CHALEPAKIS, G ;
FRITSCH, R ;
FICKENSCHER, H ;
DEUTSCH, U ;
GOULDING, M ;
GRUSS, P .
CELL, 1991, 66 (05) :873-884