Literature DB >> 10564236

Functional analysis of aquaporin-2 mutants associated with nephrogenic diabetes insipidus by yeast expression.

I Shinbo1, K Fushimi, M Kasahara, K Yamauchi, S Sasaki, F Marumo.   

Abstract

Mutations of aquaporin-2 (AQP2) vasopressin water channel cause nephrogenic diabetes insipidus (NDI). It has been suggested that impaired routing of AQP2 mutants to the plasma membrane causes the disease; however, no determinations have been made of mutation-induced alterations of AQP2 channel water permeability. To address this issue, a series of AQP2 mutants were expressed in yeast, and the osmotic water permeability (P(f)) of the isolated vesicles was measured. Wild-type and mutant AQP2 were expressed equally well in vesicles. P(f) of the vesicles containing wild-type AQP2 was 22 times greater than that of the control, which was sensitive to mercury and weakly dependent on the temperature. P(f) measurements and mercury inhibition examinations suggested that mutants L22V and P262L are fully functional, whereas mutants N68S, R187C, and S216P are partially functional. In contrast, mutants N123D, T125M, T126M, A147T, and C181W had very low water permeability. Our results suggest that the structure between the third and fifth hydrophilic loops is critical for the functional integrity of the AQP2 water channel and that disruption of AQP2 water permeability by mutations may cause NDI.

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Year:  1999        PMID: 10564236     DOI: 10.1152/ajprenal.1999.277.5.F734

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  10 in total

1.  Saccharomyces cerivisiae as a model system for kidney disease: what can yeast tell us about renal function?

Authors:  Alexander R Kolb; Teresa M Buck; Jeffrey L Brodsky
Journal:  Am J Physiol Renal Physiol       Date:  2011-04-13

Review 2.  Congenital nephrogenic diabetes insipidus: the current state of affairs.

Authors:  Daniel Wesche; Peter M T Deen; Nine V A M Knoers
Journal:  Pediatr Nephrol       Date:  2012-03-17       Impact factor: 3.714

3.  New autosomal recessive mutations in aquaporin-2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytes.

Authors:  Alexandre Leduc-Nadeau; Yoann Lussier; Marie-Françoise Arthus; Michèle Lonergan; Alejandro Martinez-Aguayo; Eva Riveira-Munoz; Olivier Devuyst; Pierre Bissonnette; Daniel G Bichet
Journal:  J Physiol       Date:  2010-04-19       Impact factor: 5.182

4.  Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.

Authors:  M Kuwahara; K Iwai; T Ooeda; T Igarashi; E Ogawa; Y Katsushima; I Shinbo; S Uchida; Y Terada; M F Arthus; M Lonergan; T M Fujiwara; D G Bichet; F Marumo; S Sasaki
Journal:  Am J Hum Genet       Date:  2001-08-30       Impact factor: 11.025

Review 5.  Cell culture models and animal models for studying the patho-physiological role of renal aquaporins.

Authors:  G Tamma; G Procino; M Svelto; G Valenti
Journal:  Cell Mol Life Sci       Date:  2011-12-22       Impact factor: 9.261

Review 6.  Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.

Authors:  Serena Milano; Monica Carmosino; Andrea Gerbino; Maria Svelto; Giuseppe Procino
Journal:  Int J Mol Sci       Date:  2017-11-10       Impact factor: 5.923

7.  Structural Basis for Mutations of Human Aquaporins Associated to Genetic Diseases.

Authors:  Luisa Calvanese; Gabriella D'Auria; Anna Vangone; Lucia Falcigno; Romina Oliva
Journal:  Int J Mol Sci       Date:  2018-05-25       Impact factor: 5.923

8.  Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.

Authors:  Ramón Peces; Rocío Mena; Carlos Peces; Fernando Santos-Simarro; Luis Fernández; Sara Afonso; Pablo Lapunzina; Rafael Selgas; Julián Nevado
Journal:  Mol Genet Genomic Med       Date:  2019-02-19       Impact factor: 2.183

9.  Improved Protocol for the Production of the Low-Expression Eukaryotic Membrane Protein Human Aquaporin 2 in Pichia pastoris for Solid-State NMR.

Authors:  Rachel Munro; Jeffrey de Vlugt; Vladimir Ladizhansky; Leonid S Brown
Journal:  Biomolecules       Date:  2020-03-11

10.  Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling.

Authors:  Yılmaz Kor; Minjing Zou; Roua A Al-Rijjal; Dorota Monies; Brian F Meyer; Yufei Shi
Journal:  BMC Med Genet       Date:  2018-07-11       Impact factor: 2.103

  10 in total

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