Background The voltage-gated K+-channel KV7.1 and the subunit KCNE1, encoded by the KCNQ1 and KCNE1 genes, respectively, are responsible for termination of the cardiac action potential. In humans, mutations in these genes can predispose patients to arrhythmias and sudden cardiac death (SCD). Aim To characterize equine KV7.1/KCNE1 currents and compare them to human KV7.1/KCNE1 currents to determine whether KV7.1/KCNE1 plays a similar role in equine and human hearts. Methods mRNA encoding KV7.1 and KCNE1 was isolated from equine hearts, sequenced, and cloned into expression vectors. The channel subunits were heterologously expressed in Xenopus laevis oocytes or CHO-K1 cells and characterized using voltage-clamp techniques. Results Equine KV7.1/KCNE1 expressed in CHO-K1 cells exhibited electrophysiological properties that are overall similar to the human orthologs; however, a slower deactivation was found which could result in more open channels at fast rates. Conclusion The results suggest that the equine KV7.1/KCNE1 channel may be important for cardiac repolarization and this could indicate that horses are susceptible to SCD caused by mutations in KCNQ1 and KCNE1.
|Number of pages||8|
|Journal||Research in Veterinary Science|
|State||Published - Aug 2017|
Bibliographical noteFunding Information:
The work was supported by grants from Foreningen Kustos af 1881 , the Danish Strategic Research Foundation 101303 , the Fraenkel Foundation , the Medical Research Council 22-02-297 , the Lundbeck Foundation R9A1131 and the National Danish Foundation for Advanced Technology 97-2012-4 .
© 2017 Elsevier Ltd
- Cardiac electrophysiology
ASJC Scopus subject areas
- Veterinary (all)