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Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy

Authors :
Cynthia M. Powell
Eric J. Horstick
Michael A. Hauser
Jeremy W. Linsley
John Y. Kuwada
Hiromi Hirata
Marcy C. Speer
Kristin K. McDonald
Wilson W. Cui
Akhila G. Satish
Allison E. Ashley-Koch
Weibin Zhou
James J. Dowling
Shawn M. Sprague
Demetra S. Stamm
Clara Franzini-Armstrong
Louis Saint-Amant
Source :
Nature communications
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Excitation-contraction coupling, the process that regulates contractions by skeletal muscles, transduces changes in membrane voltage by activating release of Ca(2+) from internal stores to initiate muscle contraction. Defects in excitation-contraction coupling are associated with muscle diseases. Here we identify Stac3 as a novel component of the excitation-contraction coupling machinery. Using a zebrafish genetic screen, we generate a locomotor mutation that is mapped to stac3. We provide electrophysiological, Ca(2+) imaging, immunocytochemical and biochemical evidence that Stac3 participates in excitation-contraction coupling in muscles. Furthermore, we reveal that a mutation in human STAC3 is the genetic basis of the debilitating Native American myopathy (NAM). Analysis of NAM stac3 in zebrafish shows that the NAM mutation decreases excitation-contraction coupling. These findings enhance our understanding of both excitation-contraction coupling and the pathology of myopathies.

Details

ISSN :
20411723
Volume :
4
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....a41c204619e8409e16a1a6e544671427