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UNC-80和NCA离子通道导致突触素突变体中的内吞作用缺陷。

UNC-80 and the NCA ion channels contribute to endocytosis defects in synaptojanin mutants.

作者信息

Jospin Maelle, Watanabe Shigeki, Joshi Deepa, Young Sean, Hamming Kevin, Thacker Colin, Snutch Terrance P, Jorgensen Erik M, Schuske Kim

机构信息

Department of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112-0840, USA.

出版信息

Curr Biol. 2007 Sep 18;17(18):1595-600. doi: 10.1016/j.cub.2007.08.036. Epub 2007 Sep 6.

Abstract

Synaptojanin is a lipid phosphatase required to degrade phosphatidylinositol 4,5 bisphosphate (PIP(2)) at cell membranes during synaptic vesicle recycling. Synaptojanin mutants in C. elegans are severely uncoordinated and are depleted of synaptic vesicles, possibly because of accumulation of PIP(2). To identify proteins that act downstream of PIP(2) 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, which are homologs of the vertebrate cation leak channel NALCN, 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.

摘要

突触素是一种脂质磷酸酶,在突触小泡循环过程中,它对于降解细胞膜上的磷脂酰肌醇4,5 - 二磷酸(PIP(2))是必需的。秀丽隐杆线虫中的突触素突变体严重不协调,并且突触小泡耗尽,这可能是由于PIP(2)的积累所致。为了鉴定在胞吞作用期间作用于PIP(2)下游的蛋白质,我们在秀丽隐杆线虫中筛选了突触素突变体的抑制子。一类称为“昏厥者”的不协调突变体部分抑制了突触素突变体中的运动、小泡耗尽和电生理缺陷。这些抑制子位点包括NCA离子通道的基因,它们是脊椎动物阳离子泄漏通道NALCN的同源物,以及一个名为unc - 80的新基因。我们证明unc - 80编码一种新的但高度保守的神经元蛋白,该蛋白是NCA - 1和NCA - 2离子通道亚基正确定位所必需的。这些数据表明,突触素突变体中NCA离子通道的激活导致突触小泡循环缺陷。

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