Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry

M. J. Alonso, D. Heine-Suñer, M. Calvo, J. Rosell, J. Giménez, M. D. Ramos, J. J. Telleria, A. Palacio, Xavier P. Estivill, Teresa Casals

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

We analyzed 1,954 Spanish cystic fibrosis (CF) alleles in order to define the molecular spectrum of mutations in the CFTR gene in Spanish CF patients. Commercial panels showed a limited detection power, leading to the identification of only 76% of alleles. Two scanning techniques, denaturing gradient gel electrophoresis (DGGE) and single strand conformation polymorphism/hetroduplex (SSCP/HD), were carried out to detect CFTR sequence changes. In addition, intragenic markers IVS8CA, IVS8-6(T)n and IVS17bTA were also analyzed. Twelve mutations showed frequencies above 1%, p.F508del being the most frequent mutation (51%). We found that eighteen mutations need to be studied to achieve a detection level of 80%. Fifty-one mutations (42%) were observed once. In total, 121 disease-causing mutations were identified, accounting for 96% (1,877 out of 1,954) of CF alleles. Specific geographic distributions for the most common mutations, p.F508del, p.G542X, c.1811 + 1.6kbA > G and c.1609delCA, were confirmed. Furthermore, two other relatively common mutations (p.V232D and c.2789 + 5G > A) showed uneven geographic distributions. This updated information on the spectrum of CF mutations in Spain will be useful for improving genetic testing, as well as to facilitate counselling in people of Spanish ancestry. In addition, this study contributes to defining the molecular spectrum of CF in Europe, and corroborates the high molecular mutation heterogeneity of Mediterranean populations.

Original languageEnglish
Pages (from-to)194-201
Number of pages8
JournalAnnals of Human Genetics
Volume71
Issue number2
DOIs
Publication statusPublished - Mar 2007
Externally publishedYes

Fingerprint

Cystic Fibrosis
Mutation
Genes
Alleles
Denaturing Gradient Gel Electrophoresis
Genetic Testing
Mutation Rate
Population Characteristics
Spain
Counseling

Keywords

  • Allelic heterogeneity
  • CFTR gene
  • Cystic fibrosis
  • Mutational spectrum

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Alonso, M. J., Heine-Suñer, D., Calvo, M., Rosell, J., Giménez, J., Ramos, M. D., ... Casals, T. (2007). Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry. Annals of Human Genetics, 71(2), 194-201. https://doi.org/10.1111/j.1469-1809.2006.00310.x

Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry. / Alonso, M. J.; Heine-Suñer, D.; Calvo, M.; Rosell, J.; Giménez, J.; Ramos, M. D.; Telleria, J. J.; Palacio, A.; Estivill, Xavier P.; Casals, Teresa.

In: Annals of Human Genetics, Vol. 71, No. 2, 03.2007, p. 194-201.

Research output: Contribution to journalArticle

Alonso, MJ, Heine-Suñer, D, Calvo, M, Rosell, J, Giménez, J, Ramos, MD, Telleria, JJ, Palacio, A, Estivill, XP & Casals, T 2007, 'Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry', Annals of Human Genetics, vol. 71, no. 2, pp. 194-201. https://doi.org/10.1111/j.1469-1809.2006.00310.x
Alonso, M. J. ; Heine-Suñer, D. ; Calvo, M. ; Rosell, J. ; Giménez, J. ; Ramos, M. D. ; Telleria, J. J. ; Palacio, A. ; Estivill, Xavier P. ; Casals, Teresa. / Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry. In: Annals of Human Genetics. 2007 ; Vol. 71, No. 2. pp. 194-201.
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