A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Beck, E.S., Gasque, G., Imlach, W.L., Jiao, W., Jiwon Choi, B., Wu, P.S., Kraushar, M.L., McCabe, B.D. (2012). Regulation of Fasciclin II and Synaptic Terminal Development by the Splicing Factor Beag.  J. Neurosci. 32(20): 7058--7073. (Export to RIS)
FlyBase ID FBrf0218385
Publication Type Research paper
PubMed ID 22593074
PubMed Abstract Pre-mRNA alternative splicing is an important mechanism for the generation of synaptic protein diversity, but few factors governing this process have been identified. From a screen for Drosophila mutants with aberrant synaptic development, we identified beag, a mutant with fewer synaptic boutons and decreased neurotransmitter release. Beag encodes a spliceosomal protein similar to splicing factors in humans and Caenorhabditis elegans. We find that both beag mutants and mutants of an interacting gene dsmu1 have changes in the synaptic levels of specific splice isoforms of Fasciclin II (FasII), the Drosophila ortholog of neural cell adhesion molecule. We show that restoration of one splice isoform of FasII can rescue synaptic morphology in beag mutants while expression of other isoforms cannot. We further demonstrate that this FasII isoform has unique functions in synaptic development independent of transsynaptic adhesion. beag and dsmu1 mutants demonstrate an essential role for these previously uncharacterized splicing factors in the regulation of synapse development and function.
DOI 10.1523/JNEUROSCI.3717-11.2012
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Language of Publication English
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Publication Type Journal
Abbreviation J. Neurosci.
Title Journal of Neuroscience
Publication Year 1981-
ISBN/ISSN 0270-6474 1529-2401
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