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Suppressive interactions between mutations located in the two nucleotide binding domains of CFTR
Author(s) -
Wei Lin,
Vankeerberghen Anne,
Jaspers Martine,
Cassiman Jean-Jacques,
Nilius Bernd,
Cuppens Harry
Publication year - 2000
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(00)01519-2
Subject(s) - wild type , xenopus , chloride channel , locus (genetics) , allele , chemistry , microbiology and biotechnology , genetics , biology , gene , mutant , biochemistry
The S1235R locus in CFTR was studied in combination with alleles found at the M470V and G628R loci. While R628 caused a maturational defect, R1235 did not. The impact of R1235 was found to be influenced by the alleles present at the G628R and M470V loci. At the single channel level, R1235‐V (R1235 on a V470 background) was characterized by an open probability significantly higher than V470‐wildtype CFTR. M470, which on its own increases CFTR chloride transport activity when compared to V470‐wildtype CFTR, suppressed the activity of R1235 in such a way that a protein with an open probability not significantly different from V470‐wildtype CFTR was obtained. While R628‐V CFTR had similar current densities as V470‐wildtype CFTR in Xenopus laevis oocytes, R1235‐V resulted in current densities that were more than twofold higher than those of V470‐wildtype CFTR. However, the current densities generated by R1235/R628‐V (R1235 and R628 on a V470 background) CFTR were significant lower than R1235‐V or R628‐V CFTR.