Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1

Stephen C Harmer, Jagdeep S Mohal, Alice A Royal, William J McKenna, Pier D Lambiase, Andrew Tinker

Research output: Contribution to journalArticle (Academic Journal)peer-review

2 Downloads (Pure)

Abstract

The KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, member 1) gene encodes the Kv7.1 potassium channel which forms a complex with KCNE1 (potassium voltage-gated channel Isk-related family member 1) in the human heart to produce the repolarizing IKs (slow delayed rectifier potassium current). Mutations in KCNQ1 can perturb IKs function and cause LQT1 (long QT syndrome type 1). In LQT1, compound mutations are relatively common and are associated with increased disease severity. LQT1 compound mutations have been shown to increase channel dysfunction, but whether other disease mechanisms, such as defective channel trafficking, contribute to the increase in arrhythmic risk has not been determined. Using an imaging-based assay we investigated the effects of four compound heterozygous mutations (V310I/R594Q, A341V/P127T, T391I/Q530X and A525T/R518X), one homozygous mutation (W248F) and one novel compound heterozygous mutation (A178T/K422fs39X) (where fs denotes frameshift) on channel trafficking. By analysing the effects in the equivalent of a homozygous, heterozygous and compound heterozygous condition, we identify three different types of behaviour. A341V/P127T and W248F/W248F had no effect, whereas V310I/R594Q had a moderate, but not compound, effect on channel trafficking. In contrast, T391I/Q530X, A525T/R518X and A178T/K422fs39X severely disrupted channel trafficking when expressed in compound form. In conclusion, we have characterized the disease mechanisms for six LQT1 compound mutations and report that, for four of these, defective channel trafficking underlies the severe clinical phenotype.

Original languageEnglish
Pages (from-to)133-42
Number of pages10
JournalBiochemical Journal
Volume462
Issue number1
DOIs
Publication statusPublished - 15 Aug 2014

Keywords

  • Animals
  • Arrhythmias, Cardiac/etiology
  • CHO Cells
  • Cricetulus
  • Genetic Predisposition to Disease
  • Heterozygote
  • Humans
  • KCNQ1 Potassium Channel/genetics
  • Long QT Syndrome/complications
  • Mutation
  • Patch-Clamp Techniques
  • Potassium Channels, Voltage-Gated/genetics

Fingerprint Dive into the research topics of 'Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1'. Together they form a unique fingerprint.

Cite this