Literature DB >> 10213643

Mutations in autosomal dominant polycystic kidney disease 2 gene: Reduced expression of PKD2 protein in lymphoblastoid cells.

G Aguiari1, E Manzati, L Penolazzi, F Micheletti, G Augello, E D Vitali, G Cappelli, Y Cai, D Reynolds, S Somlo, R Piva, L del Senno.   

Abstract

The polycystic kidney disease 2 (PKD2) gene, encoding a 968-amino acid integral membrane protein with six predicted membrane-spanning domains and intracellular NH2 and COOH termini, is mutated in approximately 15% of the cases of autosomal dominant polycystic kidney disease (ADPKD), a common genetic disease frequently resulting in renal failure. For a better understanding of the cause of this disorder, we searched for mutations in the PKD2 gene in two PKD2-linked families characterized by different clinical phenotypes. A common polymorphism, a nonsense mutation, and a frameshift mutation were found. Both mutations are predicted to produce truncated proteins of 314 and 386 amino acids, arrested at the first extracellular loop of the protein. Restriction enzyme analysis of polymerase chain reaction (PCR) and reverse transcriptase (RT)-PCR products, respectively, showed that mutations cosegregated with the disease and mutated alleles were expressed at the messenger RNA level in lymphoblastoid cell lines. However, in these cells, Western blot analysis showed only PKD2 normal protein, and it was expressed at a lower level than that found in cells without the PKD2 mutation. These findings suggest that in lymphoblastoid cells, the truncated protein product of the mutant allele may not be stable.

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Year:  1999        PMID: 10213643     DOI: 10.1016/s0272-6386(99)70420-8

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  3 in total

Review 1.  Cytopenia in autosomal dominant polycystic kidney disease (ADPKD): merely an association or a disease-related feature with prognostic implications?

Authors:  Pieter Schellekens; Willem Roosens; Bert Bammens; Djalila Mekahli; Isabelle Meyts; Rudi Vennekens
Journal:  Pediatr Nephrol       Date:  2021-01-27       Impact factor: 3.714

2.  High Resolution Melt analysis for mutation screening in PKD1 and PKD2.

Authors:  Stanislas Bataille; Yvon Berland; Michel Fontes; Stéphane Burtey
Journal:  BMC Nephrol       Date:  2011-10-18       Impact factor: 2.388

3.  Predicting a double mutant in the twilight zone of low homology modeling for the skeletal muscle voltage-gated sodium channel subunit beta-1 (Nav1.4 β1).

Authors:  Thomas Scior; Bertin Paiz-Candia; Ángel A Islas; Alfredo Sánchez-Solano; Lourdes Millan-Perez Peña; Claudia Mancilla-Simbro; Eduardo M Salinas-Stefanon
Journal:  Comput Struct Biotechnol J       Date:  2015-03-27       Impact factor: 7.271

  3 in total

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