Polyvariant mutant CFTR genes in patients with chronic pancreatitis

Citation
C. Arduino et al., Polyvariant mutant CFTR genes in patients with chronic pancreatitis, CLIN GENET, 56(5), 1999, pp. 400-404
Citations number
19
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics
Journal title
CLINICAL GENETICS
ISSN journal
00099163 → ACNP
Volume
56
Issue
5
Year of publication
1999
Pages
400 - 404
Database
ISI
SICI code
0009-9163(199911)56:5<400:PMCGIP>2.0.ZU;2-H
Abstract
Several authors have reported an association between mutations of the cysti c fibrosis transmembrane conductance regulator gene (CFTR) and chronic panc reatitis. CFTR gene transcription and protein efficiency are influenced by two polymorphic loci, (TC)m and M470V, other than the T5 allele, whose role is already well-established. The TG11/T5 haplotype is commonly found in he althy subjects, while the TG12/T5/V470 and TG13/T5/V470 haplotypes are pres ent in congenital bilateral absence of the vas deferens (CBAVD) patients. W hile the T5 allele is a mutation that is over-represented in patients with chronic pancreatitis, no data are available concerning the possible allelic preference at the other two polymorphic loci, (TG)m and M470V, in these pa tients. For this reason, we screened 39 patients with chronic pancreatitis for the most common CFTR mutations found so far in the Italian population; in addition, we examined the length of the polypyrimidine (poly-T) tract in intron 8, the (TG)m length and the M or V codon at position 470. CFTR muta tions were found in 3 patients. Poly-T variant typing identified genotype T 5/T7 in 5 patients and T5/T9 in 1 patient. Direct sequencing of intron 8 in patients with the T5 variant revealed the TG12/T5/V470 parallel to TG11/T7 /V470 genotype in 5 patients and TG10/ T9 parallel to TG11/T5 genotype in 1 patient. In patients with chronic pancreatitis, the T5 allele is frequentl y associated with TG12 and V470, a haplotype already reported in CBAVD case s and quite uncommon in healthy subjects.