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秀丽隐杆线虫中RAB - 3和RAB - 27对突触传递的调节作用

Regulation of synaptic transmission by RAB-3 and RAB-27 in Caenorhabditis elegans.

作者信息

Mahoney Timothy R, Liu Qiang, Itoh Takashi, Luo Shuo, Hadwiger Gayla, Vincent Rose, Wang Zhao-Wen, Fukuda Mitsunori, Nonet Michael L

机构信息

Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Mol Biol Cell. 2006 Jun;17(6):2617-25. doi: 10.1091/mbc.e05-12-1170. Epub 2006 Mar 29.

Abstract

Rab small GTPases are involved in the transport of vesicles between different membranous organelles. RAB-3 is an exocytic Rab that plays a modulatory role in synaptic transmission. Unexpectedly, mutations in the Caenorhabditis elegans RAB-3 exchange factor homologue, aex-3, cause a more severe synaptic transmission defect as well as a defecation defect not seen in rab-3 mutants. We hypothesized that AEX-3 may regulate a second Rab that regulates these processes with RAB-3. We found that AEX-3 regulates another exocytic Rab, RAB-27. Here, we show that C. elegans RAB-27 is localized to synapse-rich regions pan-neuronally and is also expressed in intestinal cells. We identify aex-6 alleles as containing mutations in rab-27. Interestingly, aex-6 mutants exhibit the same defecation defect as aex-3 mutants. aex-6; rab-3 double mutants have behavioral and pharmacological defects similar to aex-3 mutants. In addition, we demonstrate that RBF-1 (rabphilin) is an effector of RAB-27. Therefore, our work demonstrates that AEX-3 regulates both RAB-3 and RAB-27, that both RAB-3 and RAB-27 regulate synaptic transmission, and that RAB-27 potentially acts through its effector RBF-1 to promote soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) function.

摘要

Rab小GTP酶参与不同膜性细胞器之间的囊泡运输。RAB - 3是一种外排性Rab,在突触传递中起调节作用。出乎意料的是,秀丽隐杆线虫RAB - 3交换因子同源物aex - 3的突变会导致更严重的突触传递缺陷以及rab - 3突变体中未出现的排便缺陷。我们推测AEX - 3可能调节另一种Rab,它与RAB - 3共同调节这些过程。我们发现AEX - 3调节另一种外排性Rab,RAB - 27。在此,我们表明秀丽隐杆线虫RAB - 27在全神经元范围内定位于富含突触的区域,并且也在肠道细胞中表达。我们鉴定出aex - 6等位基因含有rab - 27的突变。有趣的是,aex - 6突变体表现出与aex - 3突变体相同的排便缺陷。aex - 6;rab - 3双突变体具有与aex - 3突变体相似的行为和药理学缺陷。此外,我们证明RBF - 1(rabphilin)是RAB - 27的效应器。因此,我们的工作表明AEX - 3调节RAB - 3和RAB - 27,RAB - 3和RAB - 27都调节突触传递,并且RAB - 27可能通过其效应器RBF - 1促进可溶性N - 乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)的功能。

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