Transcriptional regulation by WT1 in development

被引:94
作者
Roberts, SGE [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.gde.2005.08.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Wilms' tumour suppressor protein, WT1, plays a central role in the development of the genitourinary system and also other organs and tissues. WT1 can act as a transcriptional regulator or as an RNA processing factor in an isoform-dependent manner. The mechanisms that are used by WT1 to regulate transcription, and its associated target genes have been difficult to study, in part because the transcription function of WT1 is highly context-dependent. Recent studies have provided new insights into how WT1 achieves this specificity and have uncovered new target genes that are regulated by WT1 during development. In addition, ongoing studies of transgenic animals and analyses in kidney explant systems have revealed further roles for WT1 in development.
引用
收藏
页码:542 / 547
页数:6
相关论文
共 43 条
[1]   BASP1 is a transcriptional cosuppressor for the Wilms' tumor suppressor protein WT1 [J].
Carpenter, B ;
Hill, KJ ;
Charalambous, M ;
Wagner, KJ ;
Lahiri, D ;
James, DI ;
Andersen, JS ;
Schumacher, V ;
Royer-Pokora, B ;
Mann, M ;
Ward, A ;
Roberts, SGE .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (02) :537-549
[2]   Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours [J].
Dallosso, AR ;
Hancock, AL ;
Brown, KW ;
Williams, AC ;
Jackson, S ;
Malik, K .
HUMAN MOLECULAR GENETICS, 2004, 13 (04) :405-415
[3]   Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation [J].
Davies, JA ;
Ladomery, M ;
Hohenstein, P ;
Michael, L ;
Shafe, A ;
Spraggon, L ;
Hastie, N .
HUMAN MOLECULAR GENETICS, 2004, 13 (02) :235-246
[4]   Insights into the physiological role of WT1 from studies of genetically modified mice [J].
Discenza, MT ;
Pelletier, J .
PHYSIOLOGICAL GENOMICS, 2004, 16 (03) :287-300
[5]   WT1 is a modifier of the Pax2 mutant phenotype: cooperation and interaction between WT1 and Pax2 [J].
Discenza, MT ;
He, SJ ;
Lee, TH ;
Chu, LL ;
Bolon, B ;
Goodyer, P ;
Eccles, M ;
Pelletier, J .
ONCOGENE, 2003, 22 (50) :8145-8155
[6]   Apoptosis by Par-4 in cancer and neurodegenerative diseases [J].
El-Guendy, N ;
Rangnekar, VM .
EXPERIMENTAL CELL RESEARCH, 2003, 283 (01) :51-66
[7]   The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome [J].
Gao, F ;
Maiti, S ;
Sun, GZ ;
Ordonez, NG ;
Udtha, M ;
Deng, JM ;
Behringer, RR ;
Huff, V .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (22) :9899-9910
[8]   The receptor tyrosine kinase regulator sprouty1 is a target of the tumor suppressor WT1 and important for kidney development [J].
Gross, I ;
Morrison, DJ ;
Hyink, DP ;
Georgas, K ;
English, MA ;
Mericskay, M ;
Hosono, S ;
Sasson, D ;
Wilson, PD ;
Little, M ;
Licht, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) :41420-41430
[9]   WT1 activates a glomerular-specific enhancer identified from the human nephrin gene [J].
Guo, G ;
Morrison, DJ ;
Licht, JD ;
Quaggin, SE .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (11) :2851-2856
[10]   WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis [J].
Guo, JK ;
Menke, AL ;
Gubler, MC ;
Clarke, AR ;
Harrison, D ;
Hammes, A ;
Hastie, ND ;
Schedl, A .
HUMAN MOLECULAR GENETICS, 2002, 11 (06) :651-659