Abstract
The Wilms' tumour gene, WT1, encodes a protein with four zinc fingers that is probably a transcription factor. In humans, WT1 mutations can lead to childhood kidney tumours and to developmental defects of the kidney and gonad. The WT1 gene may have a role in the mesenchyme to epithelial switch in a range of mesodermally derived tissues. Furthermore, growth-factor genes may be targets for repression by the WT1 protein during development. WT1 is the first example of a tumour-suppressor gene with a specific developmental role.
Original language | English |
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Pages (from-to) | 408-13 |
Number of pages | 6 |
Journal | Current Opinion in Genetics and Development |
Volume | 3 |
Issue number | 3 |
Publication status | Published - Jun 1993 |
Keywords / Materials (for Non-textual outputs)
- Animals
- DNA-Binding Proteins
- Genes, Wilms Tumor
- Humans
- WT1 Proteins
- Zinc Fingers