Referenced in: none

Automatically associated channels: HCN1 , HCN2

Title: Evolutionary emergence of N-glycosylation as a variable promoter of HCN channel surface expression.

Authors: Andrew P Hegle, Hamed Nazzari, Andrew Roth, Damiano Angoli, Eric A Accili

Journal, date & volume: Am. J. Physiol., Cell Physiol., 2010 May , 298, C1066-76

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20130205

Abstract
All four mammalian hyperpolarization-activated cyclic nucleotide-modulated (HCN) channel isoforms have been shown to undergo N-linked glycosylation in the brain. With the mouse HCN2 isoform as a prototype, HCN channels have further been suggested to require N-glycosylation for function, a provocative finding that would make them unique in the voltage-gated potassium channel superfamily. Here, we show that both the HCN1 and HCN2 isoforms are also predominantly N-glycosylated in the embryonic heart, where they are found in significant amounts and where HCN-mediated currents are known to regulate beating frequency. Surprisingly, we find that N-glycosylation is not required for HCN2 function, although its cell surface expression is highly dependent on the presence of N-glycans. Comparatively, disruption of N-glycosylation only modestly impacts cell surface expression of HCN1 and leaves permeation and gating functions almost unchanged. This difference between HCN1 and HCN2 is consistent with evolutionary trajectories that diverged in an isoform-specific manner after gene duplication from a common HCN ancestor that lacked N-glycosylation and was able to localize efficiently to the cell surface.