Open Access Research article

Large genomic rearrangements in the CFTR gene contribute to CBAVD

Magali Taulan123, Anne Girardet123, Caroline Guittard3, Jean-Pierre Altieri3, Carine Templin3, Christophe Beroud123, Marie des Georges13 and Mireille Claustres123*

Author Affiliations

1 INSERM, U 827, Montpellier, F-34000 France

2 Université Montpellier1, UFR de Médecine, laboratoire de GénétiqueMoléculaire, Montpellier, F-3400 France

3 CHU Montpellier, hôpital Arnaud de Villeneuve, laboratoire de Génétique Moléculaire, Montpellier, F-34000 France

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BMC Medical Genetics 2007, 8:22  doi:10.1186/1471-2350-8-22

Published: 20 April 2007



By performing extensive scanning of whole coding and flanking sequences of the CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) gene, we had previously identified point mutations in 167 out of 182 (91.7%) males with isolated congenital bilateral absence of the vas deferens (CBAVD). Conventional PCR-based methods of mutation analysis do not detect gross DNA lesions. In this study, we looked for large rearrangements within the whole CFTR locus in the 32 CBAVD patients with only one or no mutation.


We developed a semi-quantitative fluorescent PCR assay (SQF-PCR), which relies on the comparison of the fluorescent profiles of multiplex PCR fragments obtained from different DNA samples. We confirmed the gross alterations by junction fragment amplification and identified their breakpoints by direct sequencing.


We detected two large genomic heterozygous deletions, one encompassing exon 2 (c.54-5811_c.164+2186del8108ins182) [or CFTRdele2], the other removing exons 22 to 24 (c.3964-3890_c.4443+3143del9454ins5) [or CFTRdele 22_24], in two males carrying a typical CBAVD mutation on the other parental CFTR allele. We present the first bioinformatic tool for exon phasing of the CFTR gene, which can help to rename the exons and the nomenclature of small mutations according to international recommendations and to predict the consequence of large rearrangements on the open reading frame.


Identification of large rearrangements further expands the CFTR mutational spectrum in CBAVD and should now be systematically investigated. We have designed a simple test to specifically detect the presence or absence of the two rearrangements identified in this study.