Deletion of dysferlin's C2 domains reveals that every domain contributes to sarcolemmal repair and all except C2B regulate Ca2+ signalling.
Dysferlin's C2 domains have distinct and specific functions in Ca2+ signalling and sarcolemmal membrane repair in skeletal muscle.
Abstract Dysferlin is an integral membrane protein of the transverse tubules of skeletal muscle that is mutated or absent in limb girdle muscular dystrophy 2B and Miyoshi myopathy. Here we examine the role of dysferlin's seven C2 domains, C2A through C2G, in membrane repair and Ca 2+ release, as well as in targeting dysferlin to the transverse tubules of skeletal muscle. We report that deletion of either domain C2A or C2B inhibits membrane repair completely, whereas deletion of C2C, C2D, C2E, C2F or C2G causes partial loss of membrane repair that is exacerbated in the absence of extracellular Ca 2+ . Deletion of C2C, C2D, C2E, C2F or C2G also causes significant changes in Ca 2+ release, measured as the amplitude of the Ca 2+ transient before or after hypo‐osmotic shock and the appearance of Ca 2+ waves. Most deletants accumulate in endoplasmic reticulum. Only the C2A domain can be deleted without affecting dysferlin trafficking to transverse tubules, but Dysf‐ΔC2A fails to support normal Ca 2+ signalling after hypo‐osmotic shock. Our data suggest that (i) every C2 domain contributes to repair; (ii) all C2 domains except C2B regulate Ca 2+ signalling; (iii) transverse tubule localization is insufficient for normal Ca 2+ signalling; and (iv) Ca 2+ dependence of repair is mediated by C2C through C2G. Thus, dysferlin's C2 domains have distinct functions in Ca 2+ signalling and sarcolemmal membrane repair and may play distinct roles in skeletal muscle. Key points Dysferlin, a transmembrane protein containing seven C2 domains, C2A through C2G, concentrates in transverse tubules of skeletal muscle, where it stabilizes voltage‐induced Ca 2+ transients and participates in sarcolemmal membrane repair. Each of dysferlin's C2 domains except C2B regulate Ca 2+ signalling. Localization of dysferlin variants to the transverse tubules is not sufficient to support normal Ca 2+ signalling or membrane repair. Each of dysferlin's C2 domains contributes to sarcolemmal membrane repair. The Ca 2+ dependence of membrane repair is mediated by C2C through C2G. Dysferlin's C2 domains therefore have distinct functions in Ca 2+ signalling and sarcolemmal membrane repair.
Muriel et al. (Mon,) conducted a other in Limb girdle muscular dystrophy 2B and Miyoshi myopathy. Deletion of dysferlin C2 domains (C2A through C2G) vs. Wild-type dysferlin was evaluated on Membrane repair, Ca2+ release, and targeting to transverse tubules. Deletion of dysferlin's C2 domains reveals that every domain contributes to sarcolemmal repair and all except C2B regulate Ca2+ signalling.