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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
    ,
*Corresponding author for this work
  • University College London
Scholary Output:
Contribution to journal
Article
Peer-review

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

Scholary Output:
Contribution to journal
Article
Peer-review

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

Published - 12/1992

ISSN

0340-6717

Publication IDs

  • Scopus: 0027092847
  • PubMed: 1483703

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Scopus
citations
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1

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