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UNC-80 and the NCA ion channels contribute to endocytosis defects in synaptojanin mutants
被引:74
作者:
Jospin, Maelle
Watanabe, Shigeki
Joshi, Deepa
Young, Sean
Hamming, Kevin
Thacker, Colin
Snutch, Terrance P.
Jorgensen, Erik M.
Schuske, Kim
机构:
[1] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[2] Univ Utah, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA
[3] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z3, Canada
关键词:
CAENORHABDITIS-ELEGANS;
ENDOPHILIN;
FAMILY;
D O I:
10.1016/j.cub.2007.08.036
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:
Synaptojanin is a lipid phosphatase required to degrade phosphatidylinositol 4,5 bisphosphate (PIP2) at cell membranes during synaptic vesicle recycling [1, 2]. Synaptojanin mutants in C. elegans are severely uncoordinated and are depleted of synaptic vesicles, possibly because of accumulation Of PIP2 [2]. To identify proteins that act downstream of PIP2 during endocytosis, we screened for suppressors of synaptojanin mutants in the nematode C. elegans. A class of uncoordinated mutants called "fainters" partially suppress the locomotory, vesicle depletion, and electrophysiological defects in synaptojanin mutants. These suppressor loci include the genes for the NCA ion channels [3], which are homologs of the vertebrate cation leak channel NALCN [4], and a novel gene called unc-80. We demonstrate that unc-80 encodes a novel, but highly conserved, neuronal protein required for the proper localization of the NCA-1 and NCA-2 ion channel subunits. These data suggest that activation of the NCA ion channel in synaptojanin mutants leads to defects in recycling of synaptic vesicles.
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页码:1595 / 1600
页数:6
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