{"title":"Who's Driving?","authors":"Joel Achenbach","doi":"10.1126/scisignal.1312002tw164","DOIUrl":null,"url":null,"abstract":"Kinesins are molecular motors that transport cargo such as proteins and membrane vesicles around the cell. In the case of a polarized cell like the neuron, kinesins ensure that cargo destined for axons or dendrites gets properly directed. However, just what \"steers\" these motors in the right direction is not clear. Setou et al. report that a binding protein of GluR2, one of the subunits of the dendritic α-amino-3-hydroxy-5-methylisoxazole-4-proprionate (AMPA) receptor, binds to the cargo-binding domain of the kinesin heavy chain. This binding protein, called glutamate-receptor-interacting protein (GRIP), colocalized with kinesin in dendritic shafts and soma of brain neurons. Kinesin also coimmunoprecipitated with GRIP and with GluR2 from dendrite-enriched subcellular brain fractions. Expression of the kinesin-binding domain of GRIP delocalized endogenous kinesin in somatodendritic regions but not in axons. A kinesin dominant negative mutant containing only the GRIP binding site reduced GRIP and GluR2 localization in synapses. Another scaffolding protein called c-Jun amino-terminal-kinase-interacting protein-1 (JIP) is known to bind to the kinesin light chain and is axon directed. Hence, traffic in neurons may be directed by categories of binding proteins that bring distinct motors and cargo together. M. Setou, D.-H. Seog, Y. Tanaka, Y. Kanai, Y. Takei, M. Kawagishi, N. Hirokawa, Glutamate-receptor-interacting protein GRIP directly steers kinesin to dendrites. Nature 417, 83-87 (2002). [Online Journal]","PeriodicalId":21619,"journal":{"name":"Science's STKE","volume":"1 1","pages":"tw164 - tw164"},"PeriodicalIF":0.0000,"publicationDate":"2002-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science's STKE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1126/scisignal.1312002tw164","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Kinesins are molecular motors that transport cargo such as proteins and membrane vesicles around the cell. In the case of a polarized cell like the neuron, kinesins ensure that cargo destined for axons or dendrites gets properly directed. However, just what "steers" these motors in the right direction is not clear. Setou et al. report that a binding protein of GluR2, one of the subunits of the dendritic α-amino-3-hydroxy-5-methylisoxazole-4-proprionate (AMPA) receptor, binds to the cargo-binding domain of the kinesin heavy chain. This binding protein, called glutamate-receptor-interacting protein (GRIP), colocalized with kinesin in dendritic shafts and soma of brain neurons. Kinesin also coimmunoprecipitated with GRIP and with GluR2 from dendrite-enriched subcellular brain fractions. Expression of the kinesin-binding domain of GRIP delocalized endogenous kinesin in somatodendritic regions but not in axons. A kinesin dominant negative mutant containing only the GRIP binding site reduced GRIP and GluR2 localization in synapses. Another scaffolding protein called c-Jun amino-terminal-kinase-interacting protein-1 (JIP) is known to bind to the kinesin light chain and is axon directed. Hence, traffic in neurons may be directed by categories of binding proteins that bring distinct motors and cargo together. M. Setou, D.-H. Seog, Y. Tanaka, Y. Kanai, Y. Takei, M. Kawagishi, N. Hirokawa, Glutamate-receptor-interacting protein GRIP directly steers kinesin to dendrites. Nature 417, 83-87 (2002). [Online Journal]
运动蛋白是一种分子马达,在细胞周围运输诸如蛋白质和膜囊泡之类的货物。在像神经元这样的极化细胞中,运动蛋白确保运往轴突或树突的货物得到正确的定向。然而,究竟是什么在正确的方向上“操纵”这些马达,目前还不清楚。Setou等人报道了树突状α-氨基-3-羟基-5-甲基异恶唑-4-proprionate (AMPA)受体的亚基之一GluR2的结合蛋白与酪蛋白重链的载货结合区域结合。这种结合蛋白被称为谷氨酸受体相互作用蛋白(GRIP),与脑神经元树突轴和胞体中的运动蛋白共定位。从富含树突的脑亚细胞部分中,酪蛋白也与GRIP和GluR2共免疫沉淀。GRIP的运动蛋白结合域的表达使内源性运动蛋白在体突区域脱位,而在轴突中不脱位。一个仅含有GRIP结合位点的激酶显性阴性突变体减少了GRIP和GluR2在突触中的定位。另一种支架蛋白称为c-Jun氨基末端激酶相互作用蛋白-1 (JIP),已知与激酶轻链结合并受轴突定向。因此,神经元的交通可能是由将不同的马达和货物结合在一起的结合蛋白类别所引导的。塞图先生,博士。Seog, Y. Tanaka, Y. Kanai, Y. Takei, M. Kawagishi, N. Hirokawa,谷氨酸受体相互作用蛋白GRIP直接引导驱动蛋白到树突。自然,417,83-87(2002)。(在线期刊)