Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1

The Wilms' tumour suppressor gene, WT1, encodes multiple nuclear protein isoforms, all containing four C-terminal zinc finger motifs. WT1 proteins can both activate and repress putative target genes in vitro, although the in vivo relevance of these putative target genes is often unverified. WT1...

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Main Authors: Sim, Edmund U. H., Smith, Aaron, Szilagi, Elida, Rae, Fiona, H Little, Melissa, Ioannou, Panos, Lindsay, Megan H
Format: E-Article
Language:English
Published: Nature Publishing Group 2002
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Online Access:http://ir.unimas.my/id/eprint/16919/1/Wnt-4%20regulation%20by%20the%20Wilms%27%20tumour%20%28abstract%29.pdf
http://ir.unimas.my/id/eprint/16919/
https://www.nature.com/onc/
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Institution: Universiti Malaysia Sarawak
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spelling my.unimas.ir.169192017-07-18T06:38:35Z http://ir.unimas.my/id/eprint/16919/ Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1 Sim, Edmund U. H. Smith, Aaron Szilagi, Elida Rae, Fiona H Little, Melissa Ioannou, Panos Lindsay, Megan H R Medicine (General) The Wilms' tumour suppressor gene, WT1, encodes multiple nuclear protein isoforms, all containing four C-terminal zinc finger motifs. WT1 proteins can both activate and repress putative target genes in vitro, although the in vivo relevance of these putative target genes is often unverified. WT1 mutations can result in Wilms' tumour and the Denys-Drash Syndrome (DDS) of infantile nephropathy, XY pseudohermaphroditism and predisposition to Wilms' tumour. We have established stable transfectants of the mouse mesonephric cell line, M15, which express WT1 harbouring a common DDS point mutation (R394W). A comparison of the expression profiles of M15 and transfectant C2A was performed using Nylon-based arrays. Very few genes showed differential expression. However Wnt-4, a member of the Wnt gene family of secreted glycoproteins, was downregulated in C2A and other similar clones. Doxycycline induction of WT1-A or WT1-D expression in HEK293 stable transfectants also elicited an elevation in Wnt4 expression. Wnt4 is critical for the mesenchyme-to-epithelial transition during kidney development, making it an attractive putative WT1 target. We have mapped human Wnt-4 gene to chromosome 1p35-36, a region of frequent LOH in WT, have characterized the genomic structure of the human Wnt-4 gene and isolated 9 kb of immediate promoter. While several potential WT1 binding sites exist within this promoter, reporter analysis does not strongly support the direct regulation of Wnt4 by WT1. We propose that Wnt-4 regulation by WT1 occurs at a more distant promoter or enhancer site, or is indirect. Nature Publishing Group 2002-06 E-Article PeerReviewed text en http://ir.unimas.my/id/eprint/16919/1/Wnt-4%20regulation%20by%20the%20Wilms%27%20tumour%20%28abstract%29.pdf Sim, Edmund U. H. and Smith, Aaron and Szilagi, Elida and Rae, Fiona and H Little, Melissa and Ioannou, Panos and Lindsay, Megan H (2002) Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1. Oncogene, 21. pp. 2948-2960. ISSN 0950-9232 https://www.nature.com/onc/ DOI: 10.1038/sj.onc.1205373
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic R Medicine (General)
spellingShingle R Medicine (General)
Sim, Edmund U. H.
Smith, Aaron
Szilagi, Elida
Rae, Fiona
H Little, Melissa
Ioannou, Panos
Lindsay, Megan H
Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
description The Wilms' tumour suppressor gene, WT1, encodes multiple nuclear protein isoforms, all containing four C-terminal zinc finger motifs. WT1 proteins can both activate and repress putative target genes in vitro, although the in vivo relevance of these putative target genes is often unverified. WT1 mutations can result in Wilms' tumour and the Denys-Drash Syndrome (DDS) of infantile nephropathy, XY pseudohermaphroditism and predisposition to Wilms' tumour. We have established stable transfectants of the mouse mesonephric cell line, M15, which express WT1 harbouring a common DDS point mutation (R394W). A comparison of the expression profiles of M15 and transfectant C2A was performed using Nylon-based arrays. Very few genes showed differential expression. However Wnt-4, a member of the Wnt gene family of secreted glycoproteins, was downregulated in C2A and other similar clones. Doxycycline induction of WT1-A or WT1-D expression in HEK293 stable transfectants also elicited an elevation in Wnt4 expression. Wnt4 is critical for the mesenchyme-to-epithelial transition during kidney development, making it an attractive putative WT1 target. We have mapped human Wnt-4 gene to chromosome 1p35-36, a region of frequent LOH in WT, have characterized the genomic structure of the human Wnt-4 gene and isolated 9 kb of immediate promoter. While several potential WT1 binding sites exist within this promoter, reporter analysis does not strongly support the direct regulation of Wnt4 by WT1. We propose that Wnt-4 regulation by WT1 occurs at a more distant promoter or enhancer site, or is indirect.
format E-Article
author Sim, Edmund U. H.
Smith, Aaron
Szilagi, Elida
Rae, Fiona
H Little, Melissa
Ioannou, Panos
Lindsay, Megan H
author_facet Sim, Edmund U. H.
Smith, Aaron
Szilagi, Elida
Rae, Fiona
H Little, Melissa
Ioannou, Panos
Lindsay, Megan H
author_sort Sim, Edmund U. H.
title Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
title_short Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
title_full Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
title_fullStr Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
title_full_unstemmed Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
title_sort wnt-4 regulation by the wilms' tumour suppressor gene, wt1
publisher Nature Publishing Group
publishDate 2002
url http://ir.unimas.my/id/eprint/16919/1/Wnt-4%20regulation%20by%20the%20Wilms%27%20tumour%20%28abstract%29.pdf
http://ir.unimas.my/id/eprint/16919/
https://www.nature.com/onc/
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