An LQTS6 MiRP1 Mutation Suppresses Pacemaker Current and is Associated with Sinus Bradycardia

Authors


  • Supported in part by the American Heart Association (Clancy), research grants HL-33843/HL-51618 (Moss) and HL-28958 (Robinson) from the National Institutes of Health, and Columbia University Department of Pediatrics.

  • No disclosures.

Address for correspondence: Richard B. Robinson, Ph.D., Department of Pharmacology, Columbia University, 630 W. 168th St., Room PS7-445, New York, NY 10032, USA. Fax: 212-305-8780; E-mail: rbr1@columbia.edu

An LQTS6 M54T Mutation and Sinus Node Dysfunction

Background

Sinus node (SN) dysfunction is observed in some long-QT syndrome (LQTS) patients, but has not been studied as a function of LQTS genotype. LQTS6 involves mutations in the hERG β-subunit MiRP1, which also interacts with hyperpolarization-activated, cyclic nucleotide gated (HCN) channels—the molecular correlate of SN pacemaker current (If). An LQTS registry search identified a 55-year male with M54T MiRP1 mutation, history of sinus bradycardia (39–56 bpm), and prolonged QTc.

Objective

We tested if LQTS6 incorporates sinus bradycardia due to abnormal If.

Methods

We transiently co-transfected neonatal rat ventricular myocytes (to study currents in a myocyte background) with human HCN4 (hHCN4, primary SN isoform) or human HCN2 (hHCN2) and one of the following: empty vector, wild-type hMiRP1 (WT), M54T hMiRP1 (M54T). Current amplitude, voltage dependence, and kinetics were measured by whole cell patch clamp.

Results

M54T co-expression decreased HCN4 current density by 80% compared to hHCN4 alone or with WT, and also slowed HCN4 activation at physiologically relevant voltages. Neither WT nor M54T altered HCN4 voltage dependence. A computer simulation predicts that these changes in HCN4 current would decrease rate and be additive with published effects of M54T mutation on hERG kinetics on rate.

Conclusions

We conclude that M54T LQTS6 mutation can cause sinus bradycardia through effects on both hERG and HCN currents. Patients with other LQTS6 mutations should be examined for SN dysfunction, and the effect on HCN current determined.

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