Unraveling the mechanisms of synapse formation and axon regeneration: the awesome power of C-elegans genetics

被引:5
|
作者
Jin YiShi [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, Howard Hughes Med Inst, San Diego, CA 92093 USA
关键词
presynaptic active zone; DLK kinase; microtubule dynamics; EFA-6; RPM-1; SYD-2; Liprin; ubiquitin E3 ligase; axon injury; laser axotomy; PRESYNAPTIC ACTIVE ZONE; SPINAL-CORD-INJURY; CAENORHABDITIS-ELEGANS; DLK-1; KINASE; RPM-1; CALCIUM; PATHWAY; PROTEIN;
D O I
10.1007/s11427-015-4962-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Since Caenorhabditis elegans was chosen as a model organism by Sydney Brenner in 1960's, genetic studies in this organism have been instrumental in discovering the function of genes and in deciphering molecular signaling network. The small size of the organism and the simple nervous system enable the complete reconstruction of the first connectome. The stereotypic developmental program and the anatomical reproducibility of synaptic connections provide a blueprint to dissect the mechanisms underlying synapse formation. Recent technological innovation using laser surgery of single axons and in vivo imaging has also made C. elegans a new model for axon regeneration. Importantly, genes regulating synaptogenesis and axon regeneration are highly conserved in function across animal phyla. This mini-review will summarize the main approaches and the key findings in understanding the mechanisms underlying the development and maintenance of the nervous system. The impact of such findings underscores the awesome power of C. elegans genetics.
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页码:1084 / 1088
页数:5
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