Voltage- and calcium-dependent BK channels regulate calcium-dependent cellular events such as neurotransmitter release by limiting calcium influx. Their plasma membrane abundance is an important factor in determining BK current and thus regulation of calcium-dependent events. In C. elegans, we show that ERG-28, an endoplasmic reticulum (ER) membrane protein, promotes the trafficking of SLO-1 BK channels from the ER to the plasma membrane by shielding them from premature degradation. In the absence of ERG-28, SLO-1 channels undergo aspartic protease DDI-1-dependent degradation, resulting in markedly reduced expression at presynaptic terminals. Loss of erg-28 suppressed phenotypic defects of slo-1 gain-of-function mutants in locomotion, neurotransmitter release, and calcium-mediated asymmetric differentiation of the AWC olfactory neuron pair, and conferred significant ethanol-resistant locomotory behavior, resembling slo-1 loss-of-function mutants, albeit to a lesser extent. Our study thus indicates that the control of BK channel trafficking is a critical regulatory mechanism for synaptic transmission and neural function. DOI: http://dx.doi.org/10.7554/eLife.24733.001
ERG-28 controls BK channel trafficking in the ER to regulate synaptic function and alcohol response in C. elegans
K. Oh,James J. Haney,Xiaohong Wang,C. Chuang,J. Richmond,Hongkyun Kim
Published 2017 in eLife
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- Publication year
2017
- Venue
eLife
- Publication date
2017-02-07
- Fields of study
Biology, Medicine
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- External record
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Semantic Scholar, PubMed
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