Novel Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family.

Background: CaM (calmodulin), encoded by 3 separate genes (, , and ), is a multifunctional Ca-binding protein involved in many signal transduction events including ion channel regulation. CaM variants may present with early-onset long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia, or sudden cardiac death. Most reported variants occurred de novo. We identified a novel variant, p.Asn138Lys (N138K), in a 4-generation family segregating with LQTS. The aim of this study was to elucidate its pathogenicity and to compare it with that of p.D130G-CaM-a variant associated with a severe LQTS phenotype.

Methods: We performed whole exome sequencing for a large, 4-generation family affected by LQTS. To assess the effect of the detected variant, the intrinsic Ca-binding affinity was measured by stoichiometric Ca titrations and equilibrium titrations. L-type Ca and slow delayed rectifier potassium currents (I and I) were recorded by whole-cell patch-clamp. Cav1.2 and Kv7.1 membrane expression were determined by optical fluorescence assays.

Results: We identified 14 p.N138K-CaM carriers in a family where 2 sudden deaths occurred in children. Several members were only mildly affected compared with CaM-LQTS patients to date described in literature. The intrinsic Ca-binding affinity of the CaM C-terminal domain was 10-fold lower for p.N138K-CaM compared with wild-type-CaM. I inactivation was slowed in cells expressing p.N138K-CaM but less than in p.D130G-CaM cells. Unexpectedly, a larger I current density was observed in cells expressing p.N138K-CaM, but not for p.D130G-CaM, compared with wild-type-CaM.

Conclusions: The p.N138K variant impairs Ca-binding affinity of CaM and I inactivation but potentiates I. The variably expressed phenotype of this variant compared with previously published de novo LQTS-CaM variants is likely explained by a milder impairment of I inactivation combined with I augmentation.