Source:http://linkedlifedata.com/resource/pubmed/id/21205795
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2011-1-5
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pubmed:abstractText |
The establishment of cell type-specific dendritic arborization patterns is a key phase in the assembly of neuronal circuitry that facilitates the integration and processing of synaptic and sensory input. Although studies in Drosophila and vertebrate systems have identified a variety of factors that regulate dendrite branch formation, the molecular mechanisms that control this process remain poorly defined. Here, we introduce the use of the Caenorhabditis elegans PVD neurons, a pair of putative nociceptors that elaborate complex dendritic arbors, as a tractable model for conducting high-throughput RNAi screens aimed at identifying key regulators of dendritic branch formation. By carrying out two separate RNAi screens, a small-scale candidate-based screen and a large-scale screen of the ~3000 genes on chromosome IV, we retrieved 11 genes that either promote or suppress the formation of PVD-associated dendrites. We present a detailed functional characterization of one of the genes, bicd-1, which encodes a microtubule-associated protein previously shown to modulate the transport of mRNAs and organelles in a variety of organisms. Specifically, we describe a novel role for bicd-1 in regulating dendrite branch formation and show that bicd-1 is likely to be expressed, and primarily required, in PVD neurons to control dendritic branching. We also present evidence that bicd-1 operates in a conserved pathway with dhc-1 and unc-116, components of the dynein minus-end-directed and kinesin-1 plus-end-directed microtubule-based motor complexes, respectively, and interacts genetically with the repulsive guidance receptor unc-5.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/5R01HD055380,
http://linkedlifedata.com/resource/pubmed/grant/R01 HD055380-03,
http://linkedlifedata.com/resource/pubmed/grant/R01NS038505,
http://linkedlifedata.com/resource/pubmed/grant/R56NS038505,
http://linkedlifedata.com/resource/pubmed/grant/T32 GM07491
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/BicD protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Caenorhabditis elegans Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cytoplasmic Dyneins,
http://linkedlifedata.com/resource/pubmed/chemical/DHC-1 protein, C elegans,
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Kinesin,
http://linkedlifedata.com/resource/pubmed/chemical/UNC-116 protein, C elegans
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1477-9129
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
138
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
507-18
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pubmed:meshHeading |
pubmed-meshheading:21205795-Animals,
pubmed-meshheading:21205795-Caenorhabditis elegans,
pubmed-meshheading:21205795-Caenorhabditis elegans Proteins,
pubmed-meshheading:21205795-Cell Cycle Proteins,
pubmed-meshheading:21205795-Cytoplasmic Dyneins,
pubmed-meshheading:21205795-Dendrites,
pubmed-meshheading:21205795-Drosophila Proteins,
pubmed-meshheading:21205795-Kinesin,
pubmed-meshheading:21205795-Protein Binding,
pubmed-meshheading:21205795-RNA Interference,
pubmed-meshheading:21205795-Sensory Receptor Cells
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pubmed:year |
2011
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pubmed:articleTitle |
C. elegans bicd-1, homolog of the Drosophila dynein accessory factor Bicaudal D, regulates the branching of PVD sensory neuron dendrites.
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pubmed:affiliation |
Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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