Two Mild Cystic Fibrosis-associated Mutations Result in Severe Cystic Fibrosis When Combined in Cisand Reveal a Residue Important for Cystic Fibrosis Transmembrane Conductance Regulator Processing and Function*

The number of complex cystic fibrosis transmembrane conductance regulator (CFTR) genotypes identified as having double-mutant alleles with two mutations inheritedin cishas been growing. We investigated the structure-function relationships of a severe cystic fibrosis (CF)-associated double mutant (R347H-D979A) to evaluate the contribution of each mild mutation to the phenotype. CFTRmutants expressed in HeLa cells were analyzed for protein biosynthesis and Cl−channel activity. Our data show that R347H is associated with mild defective Cl−channel activity and that the D979A defect leads to misprocessing. The mutant R347H-D979A combines both defects for a dramatic decrease in Cl−current. To decipher the molecular mechanism of this phenotype, single and double mutants with different charge combinations at residues 347 and 979 were constructed as charged residues were involved in this complex genotype. These studies revealed that residue 979, located in the third cytoplasmic loop, is critical for CFTR processing and Cl−channel activity highlighting the role of charged residues. These results have also important implications for CF, as they show that two mutations in ciscan act in concert to alter dramatically CFTR function contributing to the wide phenotypic variability of CF disease.