Molecular Biology and Evolution 18:1771-1788 (2001)
© 2001 Society for Molecular Biology and Evolution
A Combined Analysis of the Cystic Fibrosis Transmembrane Conductance Regulator: Implications for Structure and Disease Models
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Institut National de la Santé et de la Recherche Médicale EMI 01 15, Etablissement Français du Sang–Bretagne, Universite de Bretagne Occidentale, and Centre Hospitalier Universitaire, Brest, France;
School of Biology, University of Saint Andrews, Saint Andrews, Fife, Scotland;
Laboratoire de Biochimie-Biologie Moleculaire, CHU Angers, Angers, France;
Observatoire Océanologique, Université Pierre et Marie Curie/Centre National de la Recherche Scientifique, Banyuls-sur-Mer, France;
Institut National de la Santé et de la Recherche Médicale U458, Hôpital Robert Debré, Paris, France;
Service de Systématique Moléculaire, Museum National d'Histoire Naturelle, Paris, France
Over the past decade, nearly 1,000 variants have been identified in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in classic and atypical cystic fibrosis (CF) patients worldwide, and an enormous wealth of information concerning the structure and function of the protein has also been accumulated. These data, if evaluated together in a sequence comparison of all currently available CFTR homologs, are likely to refine the global structure-function relationship of the protein, which will, in turn, facilitate interpretation of the identified mutations in the gene. Based on such a combined analysis, we had recently defined a "functional R domain" of the CFTR protein. First, presenting two full-length cDNA sequences (termed sCFTR-I and sCFTR-II) from the Atlantic salmon (Salmo salar) and an additional partial coding sequence from the eastern gray kangaroo (Macropus giganteus), this study went further to refine the boundaries of the two nucleotide-binding domains (NBDs) and the COOH-terminal tail (C-tail), wherein NBD1 was defined as going from P439 to G646, NBD2 as going from A1225 to E1417, and the C-tail as going from E1418 to L1480. This approach also provided further insights into the differential roles of the two halves of CFTR and highlighted several well-conserved motifs that may be involved in inter- or intramolecular interactions. Moreover, a serious concern that a certain fraction of missense mutations identified in the CFTR gene may not have functional consequences was raised. Finally, phylogenetic analysis of all the full-length CFTR amino acid sequences and an extended set of exon 13–coding nucleotide sequences reinforced the idea that the rabbit may represent a better CF model than the mouse and strengthened the assertion that a long-branch attraction artifact separates the murine rodents from the rabbit and the guinea pig, the other Glires.
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