Novel vasopressin type 2 (AVPR2) gene mutations in Brazilian nephrogenic diabetes insipidus patients. 2006

W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
Department of Pharmacology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Nephrogenic diabetes insipidus (NDI) is an inherited disorder characterized by renal resistance to the antidiuretic effect of arginine vasopressin (AVP), resulting in polyuria, polydipsia, and hypoosmolar urine. In the vast majority of cases, NDI is associated with germ-line mutations in the vasopressin receptor type 2 gene (AVPR2) and in about 8% of the cases with the water channel aquaporin-2 gene (AQP-2) mutations. To date, approximately 277 families with 185 germ-line mutations in the AVPR2 gene have been described worldwide. In the present study, the AVPR2 gene was genotyped in eight unrelated Brazilian kindred with NDI. In five of these NDI families, novel mutations were noted (S54R, I130L, S187R, 219delT, and R230P), whereas three seemingly unrelated probands were found to harbor previously described AVPR2 gene mutations (R106C, R137H, R337X). Additionally a novel polymorphism (V281V) was detected. In conclusion, although NDI is a rare disease, the findings of mutations scattered over the entire coding region of the AVPR2 gene are a valuable model to determine structure function relationship in G-protein-coupled receptor related diseases. Furthermore, our data indicate that in Brazil the spectrum of AVPR2 gene mutations is "family specific".

UI MeSH Term Description Entries
D008297 Male Males
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D001938 Brazil A country located on the eastern coast of South America, located between Colombia and Peru, that borders the Atlantic Ocean. It is bordered on the north by Venezuela, Guyana, Suriname, and French Guiana, on the south by Uruguay, and on the west by Argentina. The capital is Brasilia.
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000595 Amino Acid Sequence The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION. Protein Structure, Primary,Amino Acid Sequences,Sequence, Amino Acid,Sequences, Amino Acid,Primary Protein Structure,Primary Protein Structures,Protein Structures, Primary,Structure, Primary Protein,Structures, Primary Protein
D001127 Arginine Vasopressin The predominant form of mammalian antidiuretic hormone. It is a nonapeptide containing an ARGININE at residue 8 and two disulfide-linked cysteines at residues of 1 and 6. Arg-vasopressin is used to treat DIABETES INSIPIDUS or to improve vasomotor tone and BLOOD PRESSURE. Argipressin,Vasopressin, Arginine,Arg-Vasopressin,Argipressin Tannate,Arg Vasopressin
D016366 Open Reading Frames A sequence of successive nucleotide triplets that are read as CODONS specifying AMINO ACIDS and begin with an INITIATOR CODON and end with a stop codon (CODON, TERMINATOR). ORFs,Protein Coding Region,Small Open Reading Frame,Small Open Reading Frames,sORF,Unassigned Reading Frame,Unassigned Reading Frames,Unidentified Reading Frame,Coding Region, Protein,Frame, Unidentified Reading,ORF,Open Reading Frame,Protein Coding Regions,Reading Frame, Open,Reading Frame, Unassigned,Reading Frame, Unidentified,Region, Protein Coding,Unidentified Reading Frames

Related Publications

W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
October 1992, Nature genetics,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
August 1994, American journal of human genetics,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
December 1998, Kidney international,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
August 1992, Genomics,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
November 2018, Journal of clinical research in pediatric endocrinology,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
February 2009, Journal of pediatric endocrinology & metabolism : JPEM,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
May 2008, Seminars in nephrology,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
January 1997, Nephron,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
March 1996, Pediatric research,
W L Boson, and T Della Manna, and D Damiani, and D M Miranda, and M R Gadelha, and B Liberman, and H Correa, and M A Romano-Silva, and E Friedman, and F F Silva, and P A Ribeiro, and L De Marco
April 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association,
Copied contents to your clipboard!