A low-affinity vasopressin V2-receptor gene in a kindred with X-linked nephrogenic diabetes insipidus.
Author(s) -
Kenji Yokoyama,
Akira Yamauchi,
Motomori Izumi,
T. Itoh,
A Ando,
Enyu Imai,
Tomoari Kamada,
Naohiro Ueda
Publication year - 1996
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.v73410
Subject(s) - nephrogenic diabetes insipidus , arginine vasopressin receptor 2 , vasopressin , missense mutation , arginine , endocrinology , medicine , mutant , diabetes insipidus , mutation , receptor , arginine vasopressin receptor 1b , vasopressin receptor , aquaporin 2 , chemistry , biology , gene , biochemistry , amino acid , water channel , mechanical engineering , inlet , engineering
In this study, a mutation in vasopressin Type 2 receptor (V2R) in a patient with hereditary nephrogenic diabetes insipidus (NDI) has been identified and characterized. The sequencing of the V2R gene from the patient revealed that there was a missense mutation (TAT to TGT) resulting in the substitution of 205Tyr for Cys in the putative third extracellular domain. The expression analysis in COS cells showed that the binding affinity of the mutant receptor (KD = 19.8 nM) for arginine vasopressin was much lower than that of the wild-type receptor (KD = 1.8 nM) so that intracellular cAMP production stimulated by arginine vasopressin was impaired in cells with the mutant V2R. From these results, it was concluded that the single amino-acid substitution of V2R is responsible for this familial disease.
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