Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools

Abstract Genetic access to small, reproducible sets of neurons is key to an understanding of the functional wiring of the brain. Here we report the generation of a new Gal4- and Cre-driver resource for zebrafish neurobiology. Candidate genes, including cell type-specific transcription factors, neuro...

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Autores principales: Dominique Förster, Irene Arnold-Ammer, Eva Laurell, Alison J. Barker, António M. Fernandes, Karin Finger-Baier, Alessandro Filosa, Thomas O. Helmbrecht, Yvonne Kölsch, Enrico Kühn, Estuardo Robles, Krasimir Slanchev, Tod R. Thiele, Herwig Baier, Fumi Kubo
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:4592308c86074868a69462c3c2c081a22021-12-02T15:05:24ZGenetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools10.1038/s41598-017-04657-x2045-2322https://doaj.org/article/4592308c86074868a69462c3c2c081a22017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-04657-xhttps://doaj.org/toc/2045-2322Abstract Genetic access to small, reproducible sets of neurons is key to an understanding of the functional wiring of the brain. Here we report the generation of a new Gal4- and Cre-driver resource for zebrafish neurobiology. Candidate genes, including cell type-specific transcription factors, neurotransmitter-synthesizing enzymes and neuropeptides, were selected according to their expression patterns in small and unique subsets of neurons from diverse brain regions. BAC recombineering, followed by Tol2 transgenesis, was used to generate driver lines that label neuronal populations in patterns that, to a large but variable extent, recapitulate the endogenous gene expression. We used image registration to characterize, compare, and digitally superimpose the labeling patterns from our newly generated transgenic lines. This analysis revealed highly restricted and mutually exclusive tissue distributions, with striking resolution of layered brain regions such as the tectum or the rhombencephalon. We further show that a combination of Gal4 and Cre transgenes allows intersectional expression of a fluorescent reporter in regions where the expression of the two drivers overlaps. Taken together, our study offers new tools for functional studies of specific neural circuits in zebrafish.Dominique FörsterIrene Arnold-AmmerEva LaurellAlison J. BarkerAntónio M. FernandesKarin Finger-BaierAlessandro FilosaThomas O. HelmbrechtYvonne KölschEnrico KühnEstuardo RoblesKrasimir SlanchevTod R. ThieleHerwig BaierFumi KuboNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Dominique Förster
Irene Arnold-Ammer
Eva Laurell
Alison J. Barker
António M. Fernandes
Karin Finger-Baier
Alessandro Filosa
Thomas O. Helmbrecht
Yvonne Kölsch
Enrico Kühn
Estuardo Robles
Krasimir Slanchev
Tod R. Thiele
Herwig Baier
Fumi Kubo
Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
description Abstract Genetic access to small, reproducible sets of neurons is key to an understanding of the functional wiring of the brain. Here we report the generation of a new Gal4- and Cre-driver resource for zebrafish neurobiology. Candidate genes, including cell type-specific transcription factors, neurotransmitter-synthesizing enzymes and neuropeptides, were selected according to their expression patterns in small and unique subsets of neurons from diverse brain regions. BAC recombineering, followed by Tol2 transgenesis, was used to generate driver lines that label neuronal populations in patterns that, to a large but variable extent, recapitulate the endogenous gene expression. We used image registration to characterize, compare, and digitally superimpose the labeling patterns from our newly generated transgenic lines. This analysis revealed highly restricted and mutually exclusive tissue distributions, with striking resolution of layered brain regions such as the tectum or the rhombencephalon. We further show that a combination of Gal4 and Cre transgenes allows intersectional expression of a fluorescent reporter in regions where the expression of the two drivers overlaps. Taken together, our study offers new tools for functional studies of specific neural circuits in zebrafish.
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author Dominique Förster
Irene Arnold-Ammer
Eva Laurell
Alison J. Barker
António M. Fernandes
Karin Finger-Baier
Alessandro Filosa
Thomas O. Helmbrecht
Yvonne Kölsch
Enrico Kühn
Estuardo Robles
Krasimir Slanchev
Tod R. Thiele
Herwig Baier
Fumi Kubo
author_facet Dominique Förster
Irene Arnold-Ammer
Eva Laurell
Alison J. Barker
António M. Fernandes
Karin Finger-Baier
Alessandro Filosa
Thomas O. Helmbrecht
Yvonne Kölsch
Enrico Kühn
Estuardo Robles
Krasimir Slanchev
Tod R. Thiele
Herwig Baier
Fumi Kubo
author_sort Dominique Förster
title Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
title_short Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
title_full Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
title_fullStr Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
title_full_unstemmed Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools
title_sort genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of bac transgenic tools
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/4592308c86074868a69462c3c2c081a2
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