A novel polymorphism in the coding region of the vasopressin type 2 receptor gene

Abstract

Nephrogenic diabetes insipidus (NDI) is a rare disease characterized by renal inability to respond properly to arginine vasopressin due to mutations in the vasopressin type 2 receptor (V2(R)) gene in affected kindreds. In most kindreds thus far reported, the mode of inheritance follows an X chromosome-linked recessive pattern although autosomal-dominant and autosomal-recessive modes of inheritance have also been described. Studies demonstrating mutations in the V2(R) gene in affected kindreds that modify the receptor structure, resulting in a dys- or nonfunctional receptor have been described, but phenotypically indistinguishable NDI patients with a structurally normal V2(R) gene have also been reported. In the present study, we analyzed exon 3 of the V2(R) gene in 20 unrelated individuals by direct sequencing. A C<FONT FACE="Symbol">®</font>T alteration in the third position of codon 331 (AGC<FONT FACE="Symbol">®</font>AGT), which did not alter the encoded amino acid, was found in nine individuals, including two unrelated patients with NDI. Taken together, these observations emphasize the molecular heterogeneity of a phenotypically homogeneous syndrome

vasopressin; receptor; polymorphism; diabetes insipidus; receptor gene polymorphism

Braz J Med Biol Res, April 1997, Volume 30(4) 443-445

A novel polymorphism in the coding region of the vasopressin type 2 receptor gene

J.L. Rocha¹, A. Moreira², E. Friedman³, B. Liberman⁴, B.C. Silva¹ and L. De-Marco¹

¹Departamento de Farmacologia, Universidade Federal de Minas Gerais, 31270-010 Belo Horizonte, MG, Brasil

²Departamento de Clínica Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 14049-900 Ribeirão Preto, SP, Brasil

³Department of Hematology and Genetics, Chaim Sheba Medical Center, Tel-Hashomer 52621, Israel

⁴Unidade de Endocrinologia, Hospital Brigadeiro, 01401-901 São Paulo, SP, Brasil

^Text

References

^{Correspondence and Footnotes}

Abstract

Nephrogenic diabetes insipidus (NDI) is a rare disease characterized by renal inability to respond properly to arginine vasopressin due to mutations in the vasopressin type 2 receptor (V2(R)) gene in affected kindreds. In most kindreds thus far reported, the mode of inheritance follows an X chromosome-linked recessive pattern although autosomal-dominant and autosomal-recessive modes of inheritance have also been described. Studies demonstrating mutations in the V2(R) gene in affected kindreds that modify the receptor structure, resulting in a dys- or nonfunctional receptor have been described, but phenotypically indistinguishable NDI patients with a structurally normal V2(R) gene have also been reported. In the present study, we analyzed exon 3 of the V2(R) gene in 20 unrelated individuals by direct sequencing. A C®T alteration in the third position of codon 331 (AGC®AGT), which did not alter the encoded amino acid, was found in nine individuals, including two unrelated patients with NDI. Taken together, these observations emphasize the molecular heterogeneity of a phenotypically homogeneous syndrome.

Key words: vasopressin, receptor, polymorphism, diabetes insipidus, receptor gene polymorphism

Germline mutations in the vasopressin type 2 receptor (V2(R)) gene have been demonstrated to co-segregate with nephrogenic diabetes insipidus, a rare disorder characterized by the inability to concentrate the urine due to a renal insensitivity to vasopressin.

To our knowledge, only two neutral polymorphisms have been demonstrated in this receptor gene (1,2). In addition, an A61V mutation that does not alter vasopressin binding or the stimulation of adenylate cyclase activity was also demonstrated (3). Here, we report the presence of a new polymorphism in 7 healthy Brazilian individuals, as well as in two unrelated patients with nephrogenic diabetes insipidus.

High molecular DNA was isolated from peripheral blood leukocytes according to a standard protocol (4). Based on the genomic sequence of the V2(R) gene (5), sense (5'-CAT CCT GAA CCC AAC CTA C-3') and antisense (5'-CTC TAG AGG CAA GAC ACC C-3') primers were used, as previously described (6). The polymerase chain reaction (PCR) was used to amplify this 270-bp fragment, encompassing the second intronic region and the 3' untranslated region. PCR conditions were as previously described (6). The amplified fragments were visualized by silver staining after electrophoresis on 5% polyacrylamide gel to ascertain the correct size. For direct sequencing of PCR products, the Sequenase PCR Product Sequencing kit (United States Biochemical, Cleveland, OH) was used, according to manufacturer instructions.

The data in Figure 1 show the presence of a C®T alteration in the third base of codon 331 for serine (AGC®AGT). This homozygous alteration was found in 25% (5/20) of all individuals, including two of the three individuals with nephrogenic diabetes insipidus, thus representing a polymorphism. Four individuals were heterozygous (AGC/AGT). This alteration did not introduce or abolish any restriction site.

Figure 1
- Direct sequence analysis of the amplified genomic fragment of exon 3 of the V2(R) gene showing a polymorphism* (AGT; right panel) as well as the published sequence (AGC; left panel) of codon 331.

To date, 67 mutations have been described in unrelated nephrogenic diabetes insipidus families throughout the world (7,8). However, no significant correlation of phenotype expression with genotypic variation has been demonstrated. The point mutation (A61V) that resulted in the substitution of one hydrophobic amino acid within the transmembrane region (3) was a rare polymorphism and did not cause the disease in that patient. Therefore, possible structural variations in the sequence of a normal V2(R) gene are not accounted for in all cases of nephrogenic diabetes insipidus. Indeed, another gene, the vasopressin-regulated water channel aquaporin-2 gene, has been associated with the development of autosomal nephrogenic diabetes insipidus (9,10). The identification of a second gene involved in the development of nephrogenic diabetes insipidus clearly indicates that linkage analysis should be performed before initiating mutation analysis to define which gene should be analyzed. Despite the similar clinical phenotype of all cases of nephrogenic diabetes insipidus, the analysis of several mutations reported here and the previously described polymorphisms has not shown the presence of a hot spot for these alterations, although most mutations are located in the transmembrane domain of the gene. Detection of polymorphic regions in the genes involved in the development of the disease may provide information about mutable areas within these genes.

In summary, we described here the third polymorphism in the vasopressin type 2 receptor gene, indicating that the possible structural variations in the sequence of this gene could be used, together with linkage analysis, to help understand the pathophysiology of the hereditary forms of nephrogenic diabetes insipidus.

Address for correspondence: L. De-Marco, Departamento de Farmacologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627, 31270-010 Belo Horizonte, MG, Brasil. Fax: [phone]. E-mail: [e-mail]

Presented at the International Symposium "Neuroendocrine Control of Body Fluid Homeostasis", Ribeirão Preto, SP, Brasil, August 17-20, 1996. Research supported by FAPEMIG, CNPq and CAPES. Publication supported by FAPESP. Received November 29, 1996. Accepted January 6, 1997.

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Correspondence and Footnotes

Publication Dates

• Publication in this collection
  13 Oct 1998
• Date of issue
  Apr 1997

History

• Accepted
  06 Jan 1997
• Received
  29 Nov 1996