Titre :

Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the cftr gene

Auteur(s) :

Bergougnoux, Anne [Auteur]
Deletang, K. [Auteur]
Pommier, A. [Auteur]
Varilh, J. [Auteur]
Houriez, F. [Auteur]
Altieri, J. P. [Auteur]
Koenig, M. [Auteur]
Ferec, Claude [Auteur]
Claustres, M. [Auteur]
Lalau, Guy [Auteur]
Bienvenu, Thierry [Auteur]
Audrezet, M. P. [Auteur]
Pagin, Adrien [Auteur]
Girodon, E. [Auteur]
Raynal, C. [Auteur]
Taulan-Cadars, M. [Auteur]

Titre de la revue :

Journal of cystic fibrosis . official journal of the European Cystic Fibrosis Society

Nom court de la revue :

J. Cyst. Fibros.

Date de publication :

2018-10-30

ISSN :

1873-5010

Mot(s)-clé(s) :

Splicing alteration
Deep intronic variants
CFTR gene
Large phenotypic spectrum
Pseudo-exon inclusion

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

The CFTR genotype remains incomplete in 1% of Cystic Fibrosis (CF) cases, because only one or no disease-causing variants is detected after extended analysis. This fraction is probably higher in CFTR-Related Disorders ...
Lire la suite >The CFTR genotype remains incomplete in 1% of Cystic Fibrosis (CF) cases, because only one or no disease-causing variants is detected after extended analysis. This fraction is probably higher in CFTR-Related Disorders (CFTR-RD). Deep-intronic CFTR variants are putative candidates to fill this gap. However, the recurrence, phenotypic spectrum and full molecular characterization of newly reported variants are unknown. Minigenes and analysis of CFTR transcripts in nasal epithelial cells were used to determine the impact on CFTR splicing of intronic variants that we previously identified by next generation sequencing of the whole CFTR locus. Phenotypic data were collected in 19 patients with CF and CFTR-RD, in whom one of the deep intronic variants has been detected. Three deep-intronic variants promoted the inclusion of pseudo-exons (PE) in the CFTR transcript, hindering the synthesis of a functional protein. The c.2989-313A > T variant, detected in four patients with CF or CFTR-RD from three different families, led to the inclusion of a 118 bp PE. The c.3469-1304C > G variant promoted the inclusion of a 214 bp-PE and was identified in five patients with CF from four families. Haplotype analysis confirmed that this variant was associated with one CF chromosome of African origin. The most represented variant in our cohort was the c.3874-4522A > G, detected in 10 patients with various phenotypes, from male infertility to CF with pancreatic insufficiency. These three deep intronic CFTR variants are associated with a large phenotypic spectrum, including typical CF. They should be included in CF diagnostic testing and carrier screening strategies.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

CHU Lille
Institut Pasteur de Lille
Université de Lille

Collections :

• IMPact de l'Environnement Chimique sur la Santé humaine (IMPECS) - ULR 4483

Date de dépôt :

2022-02-02T10:24:09Z