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Novel SCA19/22‐associated KCND3 mutations disrupt human K V 4.3 protein biosynthesis and channel gating
Author(s) -
Hsiao ChengTsung,
Fu SsuJu,
Liu YoTsen,
Lu YiHsiang,
Zhong CiaoYu,
Tang ChihYung,
Soong BingWen,
Jeng ChungJiuan
Publication year - 2019
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.23865
Subject(s) - biology , mutant , gating , spinocerebellar ataxia , genetics , mutation , phenotype , gene , microbiology and biotechnology , mutagenesis , ataxia , neuroscience
Mutations in the human voltage‐gated K + channel subunit K V 4.3‐encoding KCND3 gene have been associated with the autosomal dominant neurodegenerative disorder spinocerebellar ataxia types 19 and 22 (SCA19/22). The precise pathophysiology underlying the dominant inheritance pattern of SCA19/22 remains elusive. Using cerebellar ataxia‐specific targeted next‐generation sequencing technology, we identified two novel KCND3 mutations, c.950 G>A (p.C317Y) and c.1123 C>T (p.P375S) from a cohort with inherited cerebellar ataxias in Taiwan. The patients manifested notable phenotypic heterogeneity that includes cognitive impairment. We employed in vitro heterologous expression systems to inspect the biophysical and biochemical properties of human K V 4.3 harboring the two novel mutations, as well as two previously reported but uncharacterized disease‐related mutations, c.1013 T>A (p.V338E) and c.1130 C>T (p.T377M). Electrophysiological analyses revealed that all of these SCA19/22‐associated K V 4.3 mutant channels manifested loss‐of‐function phenotypes. Protein chemistry and immunofluorescence analyses further demonstrated that these mutants displayed enhanced protein degradation and defective membrane trafficking. By coexpressing K V 4.3 wild‐type with the disease‐related mutants, we provided direct evidence showing that the mutants instigated anomalous protein biosynthesis and channel gating of K V 4.3. We propose that the dominant inheritance pattern of SCA19/22 may be explained by the dominant‐negative effects of the mutants on protein biosynthesis and voltage‐dependent gating of K V 4.3 wild‐type channel.