Title of article :
The SLO-1 BK Channel of Caenorhabditis elegans is Critical for Muscle Function and is Involved in Dystrophin-dependent Muscle Dystrophy
Author/Authors :
Maité Carre-Pierrat، نويسنده , , Karine Grisoni، نويسنده , , Kathrin Gieseler، نويسنده , , Marie-Christine Mariol، نويسنده , , Edwige Martin، نويسنده , , Maelle Jospin، نويسنده , , Bruno Allard، نويسنده , , Laurent Ségalat، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
9
From page :
387
To page :
395
Abstract :
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.
Keywords :
Nematode , Duchenne Muscular Dystrophy , Potassium channel , Dystrophin
Journal title :
Journal of Molecular Biology
Serial Year :
2006
Journal title :
Journal of Molecular Biology
Record number :
1247698
Link To Document :
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