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The Cell Death Pathway Regulates Synapse Elimination through Cleavage of Gelsolin in Caenorhabditis elegans Neurons
Abstract
© 2015 The Authors. Synapse elimination occurs in development, plasticity, and disease.
Although the importance of synapse elimination has been documented in many studies,
the molecular mechanisms underlying this process are unclear. Here, using the development
of C. elegans RME neurons as a model, we have uncovered a function for the apoptosis
pathway in synapse elimination. We find that the conserved apoptotic cell death (CED)
pathway and axonal mitochondria are required for the elimination of transiently formed
clusters of presynaptic components in RME neurons. This function of the CED pathway
involves the activation of the actin-filament-severing protein, GSNL-1. Furthermore,
we show that caspase CED-3 cleaves GSNL-1 at a conserved C-terminal region and that
the cleaved active form of GSNL-1 promotes its actin-severing ability. Our data suggest
that activation of the CED pathway contributes to selective elimination of synapses
through disassembly of the actin filament network. Meng et al. find that activation
of the cell death pathway in C. elegans neurons contributes to selective elimination
of synapses through disassembly of the actin filament network.
Type
Journal articlePermalink
https://hdl.handle.net/10161/10617Published Version (Please cite this version)
10.1016/j.celrep.2015.05.031Publication Info
Meng, Lingfeng; Mulcahy, Ben; Cook, Steven J; Neubauer, Marianna; Wan, Airong; Jin,
Yishi; & Yan, Dong (2015). The Cell Death Pathway Regulates Synapse Elimination through Cleavage of Gelsolin
in Caenorhabditis elegans Neurons. Cell Reports, 11(11). pp. 1737-1748. 10.1016/j.celrep.2015.05.031. Retrieved from https://hdl.handle.net/10161/10617.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Dong Yan
Associate Professor of Molecular Genetics and Microbiology
we are interested in understanding the molecular mechanisms underlying neural circuit
formation during development and degeneration in aging. In my lab, We use a free-living
tiny roundworm, called Caenorhabditis elegans, as a model. The defined cell lineage,
completely mapped connectome and rapid life cycle of this organism greatly facilitate
investigating nervous system at the subcellular resolution. Combining classic genetic
analysis with in vivo live imaging techn

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