KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

Makarand Deo, Yanfei Ruan, Sandeep V. Pandit, Kushal Shah, Omer Berenfeld, Andrew Blaufox, Marina Cerrone, Sami F. Noujaim, Marco Denegri, José Jalife, Silvia G. Priori

Research output: Contribution to journalArticle

Abstract

We describe a mutation (E299V) in KCNJ2, the gene that encodes the strong inward rectifier K+ channel protein (Kir2.1), in an 11-y-old boy. The unique short QT syndrome type-3 phenotype is associated with an extremely abbreviated QT interval (200 ms) on ECG and paroxysmal atrial fibrillation. Genetic screening identified an A896T substitution in a highly conserved region of KCNJ2 that resulted in a de novo mutation E299V. Whole-cell patch-clamp experiments showed that E299V presents an abnormally large outward I K1 at potentials above -55 mV (P <0.001 versus wild type) due to a lack of inward rectification. Coexpression of wild-type and mutant channels to mimic the heterozygous condition still resulted in a large outward current. Coimmunoprecipitation and kinetic analysis showed that E299V and wild-type isoforms may heteromerize and that their interaction impairs function. The homomeric assembly of E299V mutant proteins actually results in gain of function. Computer simulations of ventricular excitation and propagation using both the homozygous and heterozygous conditions at three different levels of integration (single cell, 2D, and 3D) accurately reproduced the electrocardiographic phenotype of the proband, including an exceedingly short QT interval with merging of the QRS and the T wave, absence of ST segment, and peaked T waves. Numerical experiments predict that, in addition to the short QT interval, absence of inward rectification in the E299V mutation should result in atrial fibrillation. In addition, as predicted by simulations using a geometrically accurate three-dimensional ventricular model that included theHis-Purkinje network, a slight reduction in ventricular excitability via 20% reduction of the sodium current should increase vulnerability to life-threatening ventricular tachyarrhythmia.

Original languageEnglish
Pages (from-to)4291-4296
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume110
Issue number11
DOIs
Publication statusPublished - Mar 12 2013

Fingerprint

Atrial Fibrillation
Mutation
Inwardly Rectifying Potassium Channel
Phenotype
Genetic Testing
Mutant Proteins
Tachycardia
Computer Simulation
Electrocardiography
Protein Isoforms
Sodium
Genes
Short QT Syndrome 3
Proteins

Keywords

  • Cellular electrophysiology
  • Channelopathies
  • Computer models
  • Genetics
  • Ion channels

ASJC Scopus subject areas

  • General

Cite this

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia. / Deo, Makarand; Ruan, Yanfei; Pandit, Sandeep V.; Shah, Kushal; Berenfeld, Omer; Blaufox, Andrew; Cerrone, Marina; Noujaim, Sami F.; Denegri, Marco; Jalife, José; Priori, Silvia G.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, No. 11, 12.03.2013, p. 4291-4296.

Research output: Contribution to journalArticle

Deo, Makarand ; Ruan, Yanfei ; Pandit, Sandeep V. ; Shah, Kushal ; Berenfeld, Omer ; Blaufox, Andrew ; Cerrone, Marina ; Noujaim, Sami F. ; Denegri, Marco ; Jalife, José ; Priori, Silvia G. / KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia. In: Proceedings of the National Academy of Sciences of the United States of America. 2013 ; Vol. 110, No. 11. pp. 4291-4296.
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abstract = "We describe a mutation (E299V) in KCNJ2, the gene that encodes the strong inward rectifier K+ channel protein (Kir2.1), in an 11-y-old boy. The unique short QT syndrome type-3 phenotype is associated with an extremely abbreviated QT interval (200 ms) on ECG and paroxysmal atrial fibrillation. Genetic screening identified an A896T substitution in a highly conserved region of KCNJ2 that resulted in a de novo mutation E299V. Whole-cell patch-clamp experiments showed that E299V presents an abnormally large outward I K1 at potentials above -55 mV (P <0.001 versus wild type) due to a lack of inward rectification. Coexpression of wild-type and mutant channels to mimic the heterozygous condition still resulted in a large outward current. Coimmunoprecipitation and kinetic analysis showed that E299V and wild-type isoforms may heteromerize and that their interaction impairs function. The homomeric assembly of E299V mutant proteins actually results in gain of function. Computer simulations of ventricular excitation and propagation using both the homozygous and heterozygous conditions at three different levels of integration (single cell, 2D, and 3D) accurately reproduced the electrocardiographic phenotype of the proband, including an exceedingly short QT interval with merging of the QRS and the T wave, absence of ST segment, and peaked T waves. Numerical experiments predict that, in addition to the short QT interval, absence of inward rectification in the E299V mutation should result in atrial fibrillation. In addition, as predicted by simulations using a geometrically accurate three-dimensional ventricular model that included theHis-Purkinje network, a slight reduction in ventricular excitability via 20{\%} reduction of the sodium current should increase vulnerability to life-threatening ventricular tachyarrhythmia.",
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T1 - KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

AU - Deo, Makarand

AU - Ruan, Yanfei

AU - Pandit, Sandeep V.

AU - Shah, Kushal

AU - Berenfeld, Omer

AU - Blaufox, Andrew

AU - Cerrone, Marina

AU - Noujaim, Sami F.

AU - Denegri, Marco

AU - Jalife, José

AU - Priori, Silvia G.

PY - 2013/3/12

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N2 - We describe a mutation (E299V) in KCNJ2, the gene that encodes the strong inward rectifier K+ channel protein (Kir2.1), in an 11-y-old boy. The unique short QT syndrome type-3 phenotype is associated with an extremely abbreviated QT interval (200 ms) on ECG and paroxysmal atrial fibrillation. Genetic screening identified an A896T substitution in a highly conserved region of KCNJ2 that resulted in a de novo mutation E299V. Whole-cell patch-clamp experiments showed that E299V presents an abnormally large outward I K1 at potentials above -55 mV (P <0.001 versus wild type) due to a lack of inward rectification. Coexpression of wild-type and mutant channels to mimic the heterozygous condition still resulted in a large outward current. Coimmunoprecipitation and kinetic analysis showed that E299V and wild-type isoforms may heteromerize and that their interaction impairs function. The homomeric assembly of E299V mutant proteins actually results in gain of function. Computer simulations of ventricular excitation and propagation using both the homozygous and heterozygous conditions at three different levels of integration (single cell, 2D, and 3D) accurately reproduced the electrocardiographic phenotype of the proband, including an exceedingly short QT interval with merging of the QRS and the T wave, absence of ST segment, and peaked T waves. Numerical experiments predict that, in addition to the short QT interval, absence of inward rectification in the E299V mutation should result in atrial fibrillation. In addition, as predicted by simulations using a geometrically accurate three-dimensional ventricular model that included theHis-Purkinje network, a slight reduction in ventricular excitability via 20% reduction of the sodium current should increase vulnerability to life-threatening ventricular tachyarrhythmia.

AB - We describe a mutation (E299V) in KCNJ2, the gene that encodes the strong inward rectifier K+ channel protein (Kir2.1), in an 11-y-old boy. The unique short QT syndrome type-3 phenotype is associated with an extremely abbreviated QT interval (200 ms) on ECG and paroxysmal atrial fibrillation. Genetic screening identified an A896T substitution in a highly conserved region of KCNJ2 that resulted in a de novo mutation E299V. Whole-cell patch-clamp experiments showed that E299V presents an abnormally large outward I K1 at potentials above -55 mV (P <0.001 versus wild type) due to a lack of inward rectification. Coexpression of wild-type and mutant channels to mimic the heterozygous condition still resulted in a large outward current. Coimmunoprecipitation and kinetic analysis showed that E299V and wild-type isoforms may heteromerize and that their interaction impairs function. The homomeric assembly of E299V mutant proteins actually results in gain of function. Computer simulations of ventricular excitation and propagation using both the homozygous and heterozygous conditions at three different levels of integration (single cell, 2D, and 3D) accurately reproduced the electrocardiographic phenotype of the proband, including an exceedingly short QT interval with merging of the QRS and the T wave, absence of ST segment, and peaked T waves. Numerical experiments predict that, in addition to the short QT interval, absence of inward rectification in the E299V mutation should result in atrial fibrillation. In addition, as predicted by simulations using a geometrically accurate three-dimensional ventricular model that included theHis-Purkinje network, a slight reduction in ventricular excitability via 20% reduction of the sodium current should increase vulnerability to life-threatening ventricular tachyarrhythmia.

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