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Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients
- Source :
- BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
- Publication Year :
- 2017
- Publisher :
- BMC, 2017.
-
Abstract
- Abstract Background Mutations in the KCNJ2 gene encoding the ion channel Kir2.1 have been linked to the Andersen-Tawil syndrome (ATS). Molecular genetic screening performed in a family exhibiting clinical ATS phenotypes unmasked a novel sequence variant (c.434A > G, p.Y145C) in this gene. The aim of this study was to investigate the effect of this variant on Kir2.1 ion channel functionality. Methods Mutant as well as wild type GFP tagged Kir2.1 channels were expressed in HEK293 cells. In order to examine the effect of the new variant, electrophysiological measurements were performed using patch clamp technique. Cellular localization of the mutant in comparison to the wild type ion channel was analyzed by confocal laser scanning microscopy. Results The currents of cells expressing only mutant channels or a mixture of wild type and mutant were significantly reduced compared to those expressing wild type (WT) channels (p
Details
- Language :
- English
- ISSN :
- 14712350
- Volume :
- 18
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- BMC Medical Genetics
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.b84d13964441469d91a21f0859f29f42
- Document Type :
- article
- Full Text :
- https://doi.org/10.1186/s12881-017-0472-x