The presynaptic machinery at the synapse of C. elegans

被引:19
作者
Calahorro, Fernando [1 ]
Izquierdo, Patricia G. [1 ]
机构
[1] Univ Southampton, Biol Sci, Life Sci Bldg 85, Southampton SO17 1BJ, Hants, England
关键词
C; elegans; Synapse; Synaptic proteins; Synaptogenesis; Synaptic vesicles; CA2+-DEPENDENT ACTIVATOR PROTEIN; VESICLE MEMBRANE-PROTEINS; NEUROTRANSMITTER RELEASE; SUBCELLULAR-LOCALIZATION; PLASMA-MEMBRANE; MULTIPLE ROLES; RIM PROTEINS; CA2+ SENSOR; UNC-13; SNARE;
D O I
10.1007/s10158-018-0207-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synapses are specialized contact sites that mediate information flow between neurons and their targets. Important physical interactions across the synapse are mediated by synaptic adhesion molecules. These adhesions regulate formation of synapses during development and play a role during mature synaptic function. Importantly, genes regulating synaptogenesis and axon regeneration are conserved across the animal phyla. Genetic screens in the nematode Caenorhabditis elegans have identified a number of molecules required for synapse patterning and assembly. C. elegans is able to survive even with its neuronal function severely compromised. This is in comparison with Drosophila and mice where increased complexity makes them less tolerant to impaired function. Although this fact may reflect differences in the function of the homologous proteins in the synapses between these organisms, the most likely interpretation is that many of these components are equally important, but not absolutely essential, for synaptic transmission to support the relatively undemanding life style of laboratory maintained C. elegans. Here, we review research on the major group of synaptic proteins, involved in the presynaptic machinery in C. elegans, showing a strong conservation between higher organisms and highlight how C. elegans can be used as an informative tool for dissecting synaptic components, based on a simple nervous system organization.
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页数:13
相关论文
共 139 条
[1]   SYNAPTOGYRIN-DEPENDENT MODULATION OF SYNAPTIC NEUROTRANSMISSION IN CAENORHABDITIS ELEGANS [J].
Abraham, C. ;
Bai, L. ;
Leube, R. E. .
NEUROSCIENCE, 2011, 190 :75-88
[2]   Synaptic tetraspan vesicle membrane proteins are conserved but not needed for synaptogenesis and neuronal function in Caenorhabditis elegans [J].
Abraham, Christian ;
Hutter, Harald ;
Palfreyman, Mark T. ;
Spatkowski, Gabriele ;
Weimer, Robby M. ;
Windoffer, Reinhard ;
Jorgensen, Erik M. ;
Leube, Rudolf E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (21) :8227-8232
[3]   Novel Ca2+-binding protein (CAPS) related to UNC-31 required for Ca2+-activated exocytosis [J].
Ann, K ;
Kowalchyk, JA ;
Loyet, KM ;
Martin, TFJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19637-19640
[4]   Synaptic Drosophila UNC-13 is regulated by antagonistic G-protein pathways via a proteasome-dependent degradation mechanism [J].
Aravamudan, B ;
Broadie, K .
JOURNAL OF NEUROBIOLOGY, 2003, 54 (03) :417-438
[5]   Structure of synaptophysin: A hexameric MARVEL-domain channel protein [J].
Arthur, Christopher P. ;
Stowell, Michael H. B. .
STRUCTURE, 2007, 15 (06) :707-714
[6]   The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice [J].
Augustin, I ;
Korte, S ;
Rickmann, M ;
Kretzschmar, HA ;
Südhof, TC ;
Herms, JW ;
Brose, N .
JOURNAL OF NEUROSCIENCE, 2001, 21 (01) :10-17
[7]   Munc13-1 is essential for fusion competence of glutamatergic synoptic vesicles [J].
Augustin, I ;
Rosenmund, C ;
Südhof, TC ;
Brose, N .
NATURE, 1999, 400 (6743) :457-461
[8]  
AVERY L, 1993, GENETICS, V134, P454
[9]   SYNAPSIN-I BUNDLES F-ACTIN IN A PHOSPHORYLATION-DEPENDENT MANNER [J].
BAHLER, M ;
GREENGARD, P .
NATURE, 1987, 326 (6114) :704-707
[10]   A minimal domain responsible for Munc13 activity [J].
Basu, J ;
Shen, N ;
Dulubova, I ;
Lu, J ;
Guan, R ;
Guryev, O ;
Grishin, NV ;
Rosenmund, C ;
Rizo, J .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (11) :1017-1018