The SLO-1 BK channel of Caenorhabditis elegans is critical for muscle function and is involved in dystrophin-dependent muscle dystrophy

被引:38
作者
Carre-Pierrat, M
Grisoni, K
Gieseler, K
Mariol, MC
Martin, E
Jospin, M
Allard, B
Segalat, L [1 ]
机构
[1] Univ Lyon 1, CGMC, CNRS, UMR 5534, F-69622 Villeurbanne, France
[2] Univ Lyon 1, CNRS, UMR 5123, F-69622 Villeurbanne, France
关键词
dystrophin; Duchenne muscular dystrophy; nematode; potassium channel;
D O I
10.1016/j.jmb.2006.02.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Caenorhabditis elegans SLO-1 channel belongs to the family of calcium-activated large conductance BK potassium channels. SLO-1 has been shown to be involved in neurotransmitter release and ethanol response. Here, we report that SLO-1 also has a critical role in muscles. Inactivation of the slo-1 gene in muscles leads to phenotypes similar to those caused by mutations of the dystrophin homologue dys-1. Notably, slo-1 mutations result in a progressive muscle degeneration when put into a sensitized genetic background. slo-1 localization was observed by gfp reporter gene in both the M-line and the dense bodies (Z line) of the C. elegans body-wall muscles. Using the inside-out configuration of the patch clamp technique on body-wall muscle cells of acutely dissected wild-type worms, we characterized a Ca2+-activated K+ channel that was identified unambiguously as SLO-1. Since neither the abundance nor the conductance of SLO-1 was changed significantly in dys-1 mutants compared to wild-type animals, it is likely that the inactivation of dys-1 causes a misregulation of SLO-1 All in all, these results indicate that SLO-1 function in C. elegans muscles is related to the dystrophin homologue DYS-1. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:387 / 395
页数:9
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