Referenced in: none

Automatically associated channels: Kv7.4

Title: Mechanisms of Calmodulin Regulation of Different Isoforms of Kv7.4 K+ Channels.

Authors: Choong-Ryoul Sihn, Hyo Jeong Kim, Ryan L Woltz, Vladimir Yarov-Yarovoy, Pei-Chi Yang, Jun Xu, Colleen E Clancy, Xiao-Dong Zhang, Nipavan Chiamvimonvat, Ebenezer N Yamoah

Journal, date & volume: J. Biol. Chem., 2016 Jan 29 , 291, 2499-509

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26515070

Abstract
Calmodulin (CaM), a Ca(2+)-sensing protein, is constitutively bound to IQ domains of the C termini of human Kv7 (hKv7, KCNQ) channels to mediate Ca(2+)-dependent reduction of Kv7 currents. However, the mechanism remains unclear. We report that CaM binds to two isoforms of the hKv7.4 channel in a Ca(2+)-independent manner but that only the long isoform (hKv7.4a) is regulated by Ca(2+)/CaM. Ca(2+)/CaM mediate reduction of the hKv7.4a channel by decreasing the channel open probability and altering activation kinetics. We took advantage of a known missense mutation (G321S) that has been linked to progressive hearing loss to further examine the inhibitory effects of Ca(2+)/CaM on the Kv7.4 channel. Using multidisciplinary techniques, we demonstrate that the G321S mutation may destabilize CaM binding, leading to a decrease in the inhibitory effects of Ca(2+) on the channels. Our study utilizes an expression system to dissect the biophysical properties of the WT and mutant Kv7.4 channels. This report provides mechanistic insights into the critical roles of Ca(2+)/CaM regulation of the Kv7.4 channel under physiological and pathological conditions.