Identification of connective tissue growth factor as a target of WT1 transcriptional regulation

被引:31
作者
Stanhope-Baker, P [1 ]
Williams, BRG [1 ]
机构
[1] Cleveland Clin Fdn, Dept Canc Biol, Lerner Res Inst, Cleveland, OH 44195 USA
关键词
D O I
10.1074/jbc.M004901200
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 Wilms tumor suppressor WT1 has transcription-activating and -suppressing capabilities. WT1-responsive promoters have been described; however, in large part, it remains unclear which potential downstream genes are physiologically relevant and mediate the function of WT1 in tumorigenesis and development. To identify genes regulated by WT1 in vivo, we used a dominant-negative version of WT1 to modulate WT1 activity in a Wilms tumor cell line. Screening oligonucleotide arrays with RNA from these cells uncovered a number of genes whose expression was altered by abrogation of WT1 function. Several of the genes encode members of the CCN family of growth regulators. The promoter of one of these genes, connective tissue growth factor (CTGF), is suppressed by WT1 both in its endogenous location and in reporter constructs. WT1 regulation of CTGF expression is not mediated by previously identified WT1 recognition elements and may therefore involve a novel mechanism. Our results indicate that CTGF is a bona fide target of WT1 transcriptional suppression and likely plays a role in Wilms tumorigenesis and associated disease syndromes.
引用
收藏
页码:38139 / 38150
页数:12
相关论文
共 57 条
[21]   E-cadherin is a WT1 target gene [J].
Hosono, S ;
Gross, I ;
English, MA ;
Hajra, KM ;
Fearon, ER ;
Licht, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) :10943-10953
[22]   Expression of connective tissue growth factor in human renal fibrosis [J].
Ito, Y ;
Aten, J ;
Bende, RJ ;
Oemar, BS ;
Rabelink, TJ ;
Weening, JJ ;
Goldschmeding, R .
KIDNEY INTERNATIONAL, 1998, 53 (04) :853-861
[23]  
Johnstone RW, 1996, MOL CELL BIOL, V16, P6945
[24]   PROVIRAL REARRANGEMENTS AND OVEREXPRESSION OF A NEW CELLULAR GENE (NOV) IN MYELOBLASTOSIS-ASSOCIATED VIRUS TYPE-1-INDUCED NEPHROBLASTOMAS [J].
JOLIOT, V ;
MARTINERIE, C ;
DAMBRINE, G ;
PLASSIART, G ;
BRISAC, M ;
CROCHET, J ;
PERBAL, B .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (01) :10-21
[25]  
Kato MV, 1996, ONCOGENE, V12, P1361
[26]   Identification of a family of low-affinity insulin-like growth factor binding proteins (IGFBPs): Characterization of connective tissue growth factor as a member of the IGFBP superfamily [J].
Kim, HS ;
Nagalla, SR ;
Oh, Y ;
Wilson, E ;
Roberts, CT ;
Rosenfeld, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :12981-12986
[27]  
Kireeva ML, 1996, MOL CELL BIOL, V16, P1326
[28]   Cyr61 and Fisp12 are both ECM-associated signaling molecules: Activities, metabolism, and localization during development [J].
Kireeva, ML ;
Latinkic, BV ;
Kolesnikova, TV ;
Chen, CC ;
Yang, GP ;
Abler, AS ;
Lau, LF .
EXPERIMENTAL CELL RESEARCH, 1997, 233 (01) :63-77
[29]   WT-1 IS REQUIRED FOR EARLY KIDNEY DEVELOPMENT [J].
KREIDBERG, JA ;
SARIOLA, H ;
LORING, JM ;
MAEDA, M ;
PELLETIER, J ;
HOUSMAN, D ;
JAENISCH, R .
CELL, 1993, 74 (04) :679-691
[30]   The Wilms tumor suppressor WT1 encodes a transcriptional activator of amphiregulin [J].
Lee, SB ;
Huang, K ;
Palmer, R ;
Truong, VB ;
Herzlinger, D ;
Kolquist, KA ;
Wong, J ;
Paulding, C ;
Yoon, SK ;
Gerald, W ;
Oliner, JD ;
Haber, DA .
CELL, 1999, 98 (05) :663-673