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Conditional Synaptic Vesicle Markers for Drosophila

The release of neurotransmitters from synaptic vesicles (SVs) at pre-synaptic release sites is the principle means by which information transfer between neurons occurs. Knowledge of the location of SVs within a neuron can thus provide valuable clues about the location of neurotransmitter release wit...

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Autores principales: Williams, Jessica L., Shearin, Harold K., Stowers, R. Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404611/
https://www.ncbi.nlm.nih.gov/pubmed/30635441
http://dx.doi.org/10.1534/g3.118.200975
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author Williams, Jessica L.
Shearin, Harold K.
Stowers, R. Steven
author_facet Williams, Jessica L.
Shearin, Harold K.
Stowers, R. Steven
author_sort Williams, Jessica L.
collection PubMed
description The release of neurotransmitters from synaptic vesicles (SVs) at pre-synaptic release sites is the principle means by which information transfer between neurons occurs. Knowledge of the location of SVs within a neuron can thus provide valuable clues about the location of neurotransmitter release within a neuron and the downstream neurons to which a given neuron is connected, important information for understanding how neural circuits generate behavior. Here the development and characterization of four conditional tagged SV markers for Drosophila melanogaster is presented. This characterization includes evaluation of conditionality, specificity for SV localization, and sensitivity of detection in diverse neuron subtypes. These four SV markers are genome-edited variants of the synaptic vesicle-specific protein Rab3. They depend on either the B2 or FLP recombinases for conditionality, and incorporate GFP or mCherry fluorescent proteins, or FLAG or HA epitope tags, for detection.
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spelling pubmed-64046112019-03-11 Conditional Synaptic Vesicle Markers for Drosophila Williams, Jessica L. Shearin, Harold K. Stowers, R. Steven G3 (Bethesda) Investigations The release of neurotransmitters from synaptic vesicles (SVs) at pre-synaptic release sites is the principle means by which information transfer between neurons occurs. Knowledge of the location of SVs within a neuron can thus provide valuable clues about the location of neurotransmitter release within a neuron and the downstream neurons to which a given neuron is connected, important information for understanding how neural circuits generate behavior. Here the development and characterization of four conditional tagged SV markers for Drosophila melanogaster is presented. This characterization includes evaluation of conditionality, specificity for SV localization, and sensitivity of detection in diverse neuron subtypes. These four SV markers are genome-edited variants of the synaptic vesicle-specific protein Rab3. They depend on either the B2 or FLP recombinases for conditionality, and incorporate GFP or mCherry fluorescent proteins, or FLAG or HA epitope tags, for detection. Genetics Society of America 2019-01-11 /pmc/articles/PMC6404611/ /pubmed/30635441 http://dx.doi.org/10.1534/g3.118.200975 Text en Copyright © 2019 Williams et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Williams, Jessica L.
Shearin, Harold K.
Stowers, R. Steven
Conditional Synaptic Vesicle Markers for Drosophila
title Conditional Synaptic Vesicle Markers for Drosophila
title_full Conditional Synaptic Vesicle Markers for Drosophila
title_fullStr Conditional Synaptic Vesicle Markers for Drosophila
title_full_unstemmed Conditional Synaptic Vesicle Markers for Drosophila
title_short Conditional Synaptic Vesicle Markers for Drosophila
title_sort conditional synaptic vesicle markers for drosophila
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404611/
https://www.ncbi.nlm.nih.gov/pubmed/30635441
http://dx.doi.org/10.1534/g3.118.200975
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