A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysis
- Natalie Groves(corresponding author),
- Paul N. Baird,
- Annette Hogg,
- University College London
Open access
Abstract
The Wilms' tumor predisposition gene, WT1, was analysed exon-by-exon in a variety of tumours using the single-strand conformation polymorphism (SSCP) technique. A consistent variation in the usual band pattern for exon 7 was detected in this survey. On sequencing, a silent mutation was noted in codon 313 resulting in an A→G transition in an arginine codon. The A→G transition destroys an AflIII restriction enzyme recognition site, which provides a rapid means of identifying heterozygotes at this locus. Analysis of the segregation of this polymorphism in families demonstrated a co-dominant inheritance pattern. In an analysis of 21 randomly selected individuals 25% were heterozygous at this locus, which makes this polymorphism useful in a variety of genetic analyses.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 440-442 (3 pages)Journal (Volume, Issue Number)
Human Genetics (Volume 90, Issue 4)Publication milestones
- Published - 12/1992
Publication status
ISSN
0340-6717Publication IDs
- Scopus: 0027092847
- PubMed: 1483703
