Reference Report
| Reference | |||
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| Citation | Blagburn, J.M., Alexopoulos, H., Davies, J.A., Bacon, J.P. (1999). Null mutation in shaking-B eliminates electrical, but not chemical, synapses in the Drosophila giant fiber system: a structural study. J. Comp. Neurol. 404(4): 449--458. (Export to RIS) | ||
| FlyBase ID | FBrf0106230 | ||
| Publication Type | Research paper | ||
| PubMed ID | 9987990 | ||
| PubMed Abstract | Mutations in the Drosophila shaking-B gene perturb synaptic transmission and dye coupling in the giant fiber escape system. The GAL4 upstream activation sequence system was used to express a neuronal-synaptobrevin-green fluorescent protein (nsyb-GFP) construct in the giant fibers (GFs); nsyb-GFP was localized where the GFs contact the peripherally synapsing interneurons (PSIs) and the tergotrochanteral motorneurons (TTMns). Antibody to Shaking-B protein stained plaquelike structures in the same regions of the GFs, although not all plaques colocalized with nsyb-GFP. Electron microscopy showed that the GF-TTMn and GF-PSI contacts contained many chemical synaptic release sites. These sites were interposed with extensive regions of close membrane apposition (3.25 nm +/- 0.12 separation), with faint cross striations and a single-layered array of 41-nm vesicles on the GF side of the apposition. These contacts appeared similar to rectifying electrical synapses in the crayfish and were eliminated in shaking-B2 mutants. At mutant GF-TTMn and GF-PSI contacts, chemical synapses and small regions of close membrane apposition, more similar to vertebrate gap junctions, were not affected. Gap junctions with more vertebratelike separation of membranes (1.41 nm +/- 0.08) were abundant between peripheral perineurial glial processes; these were unaffected in the mutants. | ||
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| Language of Publication | English | ||
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| Publication Type | Journal | ||
| Abbreviation | J. Comp. Neurol. | ||
| Title | Journal of Comparative Neurology | ||
| Publication Year | 1911- | ||
| ISBN/ISSN | 0021-9967 | ||
Data from Reference
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Alleles (3)
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Constructs (2)
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Genes (4)
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Insertions (2)
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Transcripts (1)
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