Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene

Raquel Rabionet, Xavier P. Estivill

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Despite the large number of genes that are expected to be involved in non-syndromal, recessive deafness, only a few have been cloned. One of these genes is GJB2, which encodes connexin 26. A frameshift mutation in this gene has been reported to be common in several populations and a carrier frequency of about 1 in 30 people has been detected in Italy and Spain. Mutation 35delG is difficult to detect because it lies within a stretch of six guanines flanked by thymines, so the deletion of one G does not create or destroy a restriction site and mutagenesis primers are not useful for this mutation. We have generated an allele specific oligonucleotide method that uses 12-mer oligonucleotides and easily discriminates between the normal and 35delG alleles. The method should permit a rapid analysis of this mutation in congenital cases (recessive or sporadic), including diagnosis and carrier detection of 35delG in the population.

Original languageEnglish
Pages (from-to)260-261
Number of pages2
JournalJournal of Medical Genetics
Volume36
Issue number3
Publication statusPublished - 1999
Externally publishedYes

Fingerprint

Deafness
Oligonucleotides
Alleles
Mutation
Genes
Frameshift Mutation
Thymine
Guanine
Mutagenesis
Spain
Italy
Population
Connexin 26

Keywords

  • Connexin 26 gene
  • Deafness
  • Mutation 35delG

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene. / Rabionet, Raquel; Estivill, Xavier P.

In: Journal of Medical Genetics, Vol. 36, No. 3, 1999, p. 260-261.

Research output: Contribution to journalArticle

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