T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity

Yoshinori Tani, Daiji Miura, Junko Kurokawa, Kazufumi Nakamura, Mamoru Oouchida, Kenji Shimizu, Tohru Ohe, Tetsushi Furukawa

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Andersen-Tawil syndrome (ATS) is a multisystem inherited disease exhibiting periodic paralysis, cardiac arrhythmias, and dysmorphic features. In this study, we characterized the KCNJ2 channels with an ATS mutation (T75M) which is associated with cardiac phenotypes of bi-directional ventricular tachycardia, syncope, and QTc prolongation. Confocal imaging of GFP-KCNJ2 fusion proteins showed that the T75M mutation impaired membrane localization of the channel protein, which was restored by co-expression of WT channels with T75M channels. Whole-cell patch-clamp experiments in CHO-K1 cells showed that the T75M mutation produced a loss-of-function of the channel. When both WT and the T75M were co-expressed, the T75M mutation showed dominant-negative effects on inward rectifier K+ current densities, with prominent suppression of outward currents at potentials between 0 mV and + 80 mV over the EK. Inside-out patch experiments in HEK293T cells revealed that co-expression of WT and the T75M channels enhanced voltage-dependent block of the channels by internal Mg2+, resulting in enhanced inward rectification at potentials 50 mV more positive than the EK. We suggest that the T75M mutation causes dominant-negative suppression of the co-expressed WT KCNJ2 channels. In addition, the T75M mutation caused alteration of gating kinetics of the mutated KCNJ2 channels, i.e., increased sensitivity to intracellular Mg2+ and resultant enhancement of inward rectification. The data presented suggest that the mutation may influence clinical features, but it does not directly show this.

Original languageEnglish
Pages (from-to)187-196
Number of pages10
JournalJournal of Molecular and Cellular Cardiology
Volume43
Issue number2
DOIs
Publication statusPublished - Aug 2007

Fingerprint

Andersen Syndrome
Mutation
Familial Mediterranean Fever
CHO Cells
Syncope
Ventricular Tachycardia
Ion Channels
Paralysis
Cardiac Arrhythmias
Proteins
Phenotype

Keywords

  • Andersen-Tawil syndrome
  • Inward rectification
  • KCNJ2
  • Magnesium
  • QT prolongation
  • Spermine
  • The Kir2.1 (I) channel

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity. / Tani, Yoshinori; Miura, Daiji; Kurokawa, Junko; Nakamura, Kazufumi; Oouchida, Mamoru; Shimizu, Kenji; Ohe, Tohru; Furukawa, Tetsushi.

In: Journal of Molecular and Cellular Cardiology, Vol. 43, No. 2, 08.2007, p. 187-196.

Research output: Contribution to journalArticle

Tani, Yoshinori ; Miura, Daiji ; Kurokawa, Junko ; Nakamura, Kazufumi ; Oouchida, Mamoru ; Shimizu, Kenji ; Ohe, Tohru ; Furukawa, Tetsushi. / T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity. In: Journal of Molecular and Cellular Cardiology. 2007 ; Vol. 43, No. 2. pp. 187-196.
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