Anthropological features of the CFTR gene: Its variability in an African population

• Published in: Annals of human biology Vol. 38; no. 2; pp. 203 - 209
• Main Authors: Maria Ciminelli, Bianca, Bombieri, Cristina, Ciccacci, Cinzia, Belpinati, Francesca, Pompei, Fiorenza, Maselli, Roberta, Simporé, Jacques, Pignatti, Pier Franco, Modiano, Guido
• Format: Journal Article
• Language: English
• Published: England Informa Healthcare 01-03-2011; Taylor & Francis
• Subjects: African Continental Ancestry Group - genetics; Alleles; Burkina Faso; Cystic Fibrosis - epidemiology; Cystic Fibrosis - ethnology; Cystic Fibrosis Transmembrane Conductance Regulator - genetics; Degree of heterozygosity; Europe - epidemiology; evolution rate; Exons - genetics; Gene Frequency; haplotype; Humans; Introns - genetics; linkage disequilibrium; Mutation; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Europe; Burkina Faso
• ISSN: 0301-4460; 1464-5033
• DOI: 10.3109/03014460.2010.507554

Background: The CFTR gene (Cystic Fibrosis conductance Transmembrane Regulator) is the gene responsible for Cystic Fibrosis, the most common severe autosomal recessive disease in Europeans. It has been extensively explored in several European and European-derived populations, but poorly studied in the other major human groups.Aim: To characterize the variability of the CFTR gene in an African population.Subjects and methods: Using DGGE, all 27 exons (4443 bp) and 2184 bp of the flanking intronic regions of the CFTR gene were studied in a random sample of 45 Mossì from Burkina Faso (Western sub-Saharan Africa).Results: Sixteen variable sites were found: 13 SNPs (one in the promoter region, four non-synonymous and five synonymous in the exons and three in the introns) and three intronic STRs. Only the promoter site ( − 94 G/T), slightly polymorphic in the present survey, was not variable in different European populations. Comparison between Western Africans, Eastern Africans, Europeans and Eastern Asians showed that alleles at two intronic STRs (Tn and (TG)m in intron 8), four exonic (M470V, 2694 T/G, 4002 A/G and 4521 G/A) and one intronic (875+40 A/G) SNPs have very different frequencies among at least two major human groups. Moreover, the overall degree of non-synonymous variability in Mossì is much lower than that in Europeans. A possible interpretation of this finding is proposed.Conclusions: The CFTR gene has been since long hypothesized to have undergone selection in Europeans. The present study by comparing Africans and Europeans for the overall variability of the gene supports this hypothesis.