Arrhythmogenic calmodulin E105A mutation alters cardiac RyR2 regulation leading to cardiac dysfunction in zebrafish

Sahar Da'as, Angelos Thanassoulas, Brian L. Calver, Konrad Beck, Rola Salem, Alaaeldin Saleh, Iris Kontogianni, Ali Al-Maraghi, Gheyath K. Nasrallah, Bared Safieh-Garabedian, Egon Toft, George Nounesis, F. Anthony Lai, Michail Nomikos

Research output: Contribution to journalArticle

Abstract

Calmodulin (CaM) is a universal calcium (Ca 2+ )-binding messenger that regulates many vital cellular events. In cardiac muscle, CaM associates with ryanodine receptor 2 (RyR2) and regulates excitation–contraction coupling. Mutations in human genes CALM1, CALM2, and CALM3 have been associated with life-threatening heart disorders, such as long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia. A novel de novo LQTS-associated missense CaM mutation (E105A) was recently identified in a 6-year-old boy, who experienced an aborted first episode of cardiac arrest. Herein, we report the first molecular characterization of the CaM E105A mutation. Expression of the CaM E105A mutant in zebrafish embryos resulted in cardiac arrhythmia and increased heart rate, suggestive of ventricular tachycardia. In vitro biophysical and biochemical analysis revealed that E105A confers a deleterious effect on protein stability and a reduced Ca 2+ -binding affinity due to loss of cooperativity. Finally, the CaM E105A mutation resulted in reduced CaM–RyR2 interaction and defective modulation of ryanodine binding. Our findings suggest that the CaM E105A mutation dysregulates normal cardiac function by a complex mechanism involving alterations in both CaM–Ca 2+ and CaM–RyR2 interactions.

Original languageEnglish
JournalAnnals of the New York Academy of Sciences
DOIs
Publication statusPublished - 1 Jan 2019

Fingerprint

Ryanodine Receptor Calcium Release Channel
Zebrafish
Calmodulin
Mutation
Long QT Syndrome
Ryanodine
Protein Stability
Missense Mutation
Ventricular Tachycardia
Heart Arrest
Muscle
Cardiac Arrhythmias
Myocardium
Embryonic Structures
Genes
Heart Rate
Modulation
Calcium

Keywords

  • arrhythmia
  • calcium
  • calmodulin
  • long QT syndrome
  • ryanodine receptor 2
  • zebrafish

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • History and Philosophy of Science

Cite this

Arrhythmogenic calmodulin E105A mutation alters cardiac RyR2 regulation leading to cardiac dysfunction in zebrafish. / Da'as, Sahar; Thanassoulas, Angelos; Calver, Brian L.; Beck, Konrad; Salem, Rola; Saleh, Alaaeldin; Kontogianni, Iris; Al-Maraghi, Ali; Nasrallah, Gheyath K.; Safieh-Garabedian, Bared; Toft, Egon; Nounesis, George; Lai, F. Anthony; Nomikos, Michail.

In: Annals of the New York Academy of Sciences, 01.01.2019.

Research output: Contribution to journalArticle

Da'as, S, Thanassoulas, A, Calver, BL, Beck, K, Salem, R, Saleh, A, Kontogianni, I, Al-Maraghi, A, Nasrallah, GK, Safieh-Garabedian, B, Toft, E, Nounesis, G, Lai, FA & Nomikos, M 2019, 'Arrhythmogenic calmodulin E105A mutation alters cardiac RyR2 regulation leading to cardiac dysfunction in zebrafish', Annals of the New York Academy of Sciences. https://doi.org/10.1111/nyas.14033
Da'as, Sahar ; Thanassoulas, Angelos ; Calver, Brian L. ; Beck, Konrad ; Salem, Rola ; Saleh, Alaaeldin ; Kontogianni, Iris ; Al-Maraghi, Ali ; Nasrallah, Gheyath K. ; Safieh-Garabedian, Bared ; Toft, Egon ; Nounesis, George ; Lai, F. Anthony ; Nomikos, Michail. / Arrhythmogenic calmodulin E105A mutation alters cardiac RyR2 regulation leading to cardiac dysfunction in zebrafish. In: Annals of the New York Academy of Sciences. 2019.
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AU - Calver, Brian L.

AU - Beck, Konrad

AU - Salem, Rola

AU - Saleh, Alaaeldin

AU - Kontogianni, Iris

AU - Al-Maraghi, Ali

AU - Nasrallah, Gheyath K.

AU - Safieh-Garabedian, Bared

AU - Toft, Egon

AU - Nounesis, George

AU - Lai, F. Anthony

AU - Nomikos, Michail

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N2 - Calmodulin (CaM) is a universal calcium (Ca 2+ )-binding messenger that regulates many vital cellular events. In cardiac muscle, CaM associates with ryanodine receptor 2 (RyR2) and regulates excitation–contraction coupling. Mutations in human genes CALM1, CALM2, and CALM3 have been associated with life-threatening heart disorders, such as long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia. A novel de novo LQTS-associated missense CaM mutation (E105A) was recently identified in a 6-year-old boy, who experienced an aborted first episode of cardiac arrest. Herein, we report the first molecular characterization of the CaM E105A mutation. Expression of the CaM E105A mutant in zebrafish embryos resulted in cardiac arrhythmia and increased heart rate, suggestive of ventricular tachycardia. In vitro biophysical and biochemical analysis revealed that E105A confers a deleterious effect on protein stability and a reduced Ca 2+ -binding affinity due to loss of cooperativity. Finally, the CaM E105A mutation resulted in reduced CaM–RyR2 interaction and defective modulation of ryanodine binding. Our findings suggest that the CaM E105A mutation dysregulates normal cardiac function by a complex mechanism involving alterations in both CaM–Ca 2+ and CaM–RyR2 interactions.

AB - Calmodulin (CaM) is a universal calcium (Ca 2+ )-binding messenger that regulates many vital cellular events. In cardiac muscle, CaM associates with ryanodine receptor 2 (RyR2) and regulates excitation–contraction coupling. Mutations in human genes CALM1, CALM2, and CALM3 have been associated with life-threatening heart disorders, such as long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia. A novel de novo LQTS-associated missense CaM mutation (E105A) was recently identified in a 6-year-old boy, who experienced an aborted first episode of cardiac arrest. Herein, we report the first molecular characterization of the CaM E105A mutation. Expression of the CaM E105A mutant in zebrafish embryos resulted in cardiac arrhythmia and increased heart rate, suggestive of ventricular tachycardia. In vitro biophysical and biochemical analysis revealed that E105A confers a deleterious effect on protein stability and a reduced Ca 2+ -binding affinity due to loss of cooperativity. Finally, the CaM E105A mutation resulted in reduced CaM–RyR2 interaction and defective modulation of ryanodine binding. Our findings suggest that the CaM E105A mutation dysregulates normal cardiac function by a complex mechanism involving alterations in both CaM–Ca 2+ and CaM–RyR2 interactions.

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