[No authors listed]
Chemical synapses are complex structures that mediate rapid intercellular signalling in the nervous system. Proteomic studies suggest that several hundred proteins will be found at synaptic specializations. Here we describe a systematic screen to identify genes required for the function or development of Caenorhabditis elegans neuromuscular junctions. A total of 185 genes were identified in an RNA interference screen for decreased acetylcholine secretion; 132 of these genes had not previously been implicated in synaptic transmission. Functional profiles for these genes were determined by comparing secretion defects observed after RNA interference under a variety of conditions. Hierarchical clustering identified groups of functionally related genes, including those involved in the synaptic vesicle cycle, neuropeptide signalling and responsiveness to phorbol esters. Twenty-four genes encoded proteins that were localized to presynaptic specializations. Loss-of-function mutations in 12 genes caused defects in presynaptic structure.
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vps-20, gsa-1, egl-30, did-2, nab-1, npp-6, apm-1, myo-1, taf-5, gska-3, rab-5, csnk-1, gsk-3, agef-1, F10C5.2, mat-3, apb-1, pbo-1, mpk-1, par-3, dlc-1, rpt-3, W09D10.1, pat-6, snn-1, eel-1, ogdh-1, miro-1, hgrs-1, rack-1, let-70, inx-8, par-5, cpsf-4, aps-1, gsp-1, spc-1, unc-78, apa-2, mrp-5, vps-32.2, miro-2, M117.3, vps-4, miro-3, Y61A9LA.5, Y71H2AL.2, Y75B8A.10, drl-1, arx-3
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