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Publication : Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulator.

First Author  Yorifuji T Year  1991
Journal  Genomics Volume  10
Issue  3 Pages  547-50
PubMed ID  1716243 Mgi Jnum  J:11413
Mgi Id  MGI:59849 Doi  10.1016/0888-7543(91)90434-g
Citation  Yorifuji T, et al. (1991) Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulator. Genomics 10(3):547-50
abstractText  We have cloned the mouse homolog of the human cystic fibrosis transmembrane conductance regulator (CFTR) using clones isolated from a mouse lung cDNA library and using amplification of cDNA to isolate specific regions. The cDNA was 6304 bp in length and encoded a polypeptide of 1476 amino acids. Comparison of the deduced amino acid sequence showed that the mouse protein has high homology to the human protein; overall identity was 78.3%. The amino acid identity was high for both transmembrane domains (first transmembrane domain, 86.7%; second transmembrane domain, 81.1%) and for both ATP-binding folds (first ATP-binding fold, 80.5%; second ATP-binding fold, 83.9%), suggesting the functional importance of these regions. On the other hand, the R domain was less well conserved (68.9% identity). All of the published missense mutation sites and the site of the common delta F508 mutation were conserved between human and mouse.
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