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Photo-labeling neurons in the Drosophila brain

Many genetically encoded tools, including large collections of GAL4 transgenic lines, can be used to visualize neurons of the Drosophila melanogaster brain. However, identifying transgenic lines that are expressed sparsely enough to label individual neurons, or groups of neurons that innervate a par...

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Detalles Bibliográficos
Autores principales: Li, Jinzhi, Ellis, Kaitlyn Elizabeth, Caron, Sophie Jeanne Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941087/
https://www.ncbi.nlm.nih.gov/pubmed/33733243
http://dx.doi.org/10.1016/j.xpro.2021.100381
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author Li, Jinzhi
Ellis, Kaitlyn Elizabeth
Caron, Sophie Jeanne Cécile
author_facet Li, Jinzhi
Ellis, Kaitlyn Elizabeth
Caron, Sophie Jeanne Cécile
author_sort Li, Jinzhi
collection PubMed
description Many genetically encoded tools, including large collections of GAL4 transgenic lines, can be used to visualize neurons of the Drosophila melanogaster brain. However, identifying transgenic lines that are expressed sparsely enough to label individual neurons, or groups of neurons that innervate a particular brain region, remains technically challenging. Here, we provide a detailed procedure in which we used broadly expressed transgenic lines and two-photon microscopy to photo-label neurons with specificity, thereby permitting their morphological characterization. For complete details on the use and execution of this protocol, please refer to Li et al. (2020).
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spelling pubmed-79410872021-03-16 Photo-labeling neurons in the Drosophila brain Li, Jinzhi Ellis, Kaitlyn Elizabeth Caron, Sophie Jeanne Cécile STAR Protoc Protocol Many genetically encoded tools, including large collections of GAL4 transgenic lines, can be used to visualize neurons of the Drosophila melanogaster brain. However, identifying transgenic lines that are expressed sparsely enough to label individual neurons, or groups of neurons that innervate a particular brain region, remains technically challenging. Here, we provide a detailed procedure in which we used broadly expressed transgenic lines and two-photon microscopy to photo-label neurons with specificity, thereby permitting their morphological characterization. For complete details on the use and execution of this protocol, please refer to Li et al. (2020). Elsevier 2021-03-06 /pmc/articles/PMC7941087/ /pubmed/33733243 http://dx.doi.org/10.1016/j.xpro.2021.100381 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Li, Jinzhi
Ellis, Kaitlyn Elizabeth
Caron, Sophie Jeanne Cécile
Photo-labeling neurons in the Drosophila brain
title Photo-labeling neurons in the Drosophila brain
title_full Photo-labeling neurons in the Drosophila brain
title_fullStr Photo-labeling neurons in the Drosophila brain
title_full_unstemmed Photo-labeling neurons in the Drosophila brain
title_short Photo-labeling neurons in the Drosophila brain
title_sort photo-labeling neurons in the drosophila brain
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941087/
https://www.ncbi.nlm.nih.gov/pubmed/33733243
http://dx.doi.org/10.1016/j.xpro.2021.100381
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