Yeh Edward, Kawano Taizo, Weimer Robby M, Bessereau Jean-Louis, Zhen Mei
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, M5G 1X5, Canada.
J Neurosci. 2005 Apr 13;25(15):3833-41. doi: 10.1523/JNEUROSCI.4978-04.2005.
Active zones are presynaptic regions where synaptic vesicles fuse with plasma membrane to release neurotransmitters. Active zones are highly organized structurally and are functionally conserved among different species. Synapse defective-2 (SYD-2) family proteins regulate active zone morphology in Caenorhabditis elegans and Drosophila. Here, we demonstrate by immunoelectron microscopy that at C. elegans synapses, SYD-2 localizes strictly at active zones and can be used as an active zone marker when fused to green fluorescent protein (GFP). By driving expression of SYD-2::GFP fusion protein in GABAergic neurons, we are able to visualize discrete fluorescent puncta corresponding to active zones in living C. elegans. During development, the number of GABAergic synapses made by specific motoneurons increases only slightly from larvae to adult stages. In contrast, the number of SYD-2::GFP puncta doubles, suggesting that individual synapses accommodate the increasing size of their synaptic targets mainly by incorporating more active zone materials. Furthermore, we used this marker to perform a genetic screen to identify genes involved in the development of active zones. We recovered 16 mutants with altered SYD-2::GFP expression, including alleles of five genes that have been implicated previously in synapse formation or nervous-system development. Mapping of 11 additional mutants suggests that they may represent novel genes involved in active zone formation.
活性区是突触前区域,突触小泡在此与质膜融合以释放神经递质。活性区在结构上高度有序,且在不同物种间功能保守。突触缺陷蛋白2(SYD - 2)家族蛋白在秀丽隐杆线虫和果蝇中调节活性区形态。在此,我们通过免疫电子显微镜证明,在秀丽隐杆线虫突触处,SYD - 2严格定位于活性区,当与绿色荧光蛋白(GFP)融合时可作为活性区标记物。通过在GABA能神经元中驱动SYD - 2::GFP融合蛋白的表达,我们能够在活的秀丽隐杆线虫中可视化对应于活性区的离散荧光点。在发育过程中,特定运动神经元形成的GABA能突触数量从幼虫到成虫阶段仅略有增加。相比之下,SYD - 2::GFP点的数量翻倍,这表明单个突触主要通过整合更多活性区物质来适应其突触靶点不断增加的大小。此外,我们使用这个标记物进行遗传筛选,以鉴定参与活性区发育的基因。我们获得了16个SYD - 2::GFP表达改变的突变体,包括先前已涉及突触形成或神经系统发育的五个基因的等位基因。对另外11个突变体的定位表明,它们可能代表参与活性区形成的新基因。