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Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos

We established a method for bioluminescence imaging (BLI) to track real-time gene expression in live Drosophila embryos. We constructed a transgenesis vector containing multiple cloning sites and enhanced green-emitting luciferase (ELuc; Emerald Luc), a brighter and pH-insensitive luciferase for pro...

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Autores principales: Akiyoshi, Ryutaro, Kaneuch, Taro, Aigaki, Toshiro, Suzuki, Hirobumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149885/
https://www.ncbi.nlm.nih.gov/pubmed/25023969
http://dx.doi.org/10.1007/s00216-014-8000-8
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author Akiyoshi, Ryutaro
Kaneuch, Taro
Aigaki, Toshiro
Suzuki, Hirobumi
author_facet Akiyoshi, Ryutaro
Kaneuch, Taro
Aigaki, Toshiro
Suzuki, Hirobumi
author_sort Akiyoshi, Ryutaro
collection PubMed
description We established a method for bioluminescence imaging (BLI) to track real-time gene expression in live Drosophila embryos. We constructed a transgenesis vector containing multiple cloning sites and enhanced green-emitting luciferase (ELuc; Emerald Luc), a brighter and pH-insensitive luciferase for promoter analysis. To evaluate the utility of BLI using an ELuc reporter together with an optimized microscope system, we visualized the expression pattern of armadillo (arm), a member of the Wnt pathway in Drosophila, throughout embryogenesis. We generated transgenic flies carrying the arm:: ELuc fusion gene, and successfully performed BLI continuously for 22 h in the same embryos. Our study showed, for the first time, that arm::Eluc expression was dramatically increased in the anterior midgut rudiment, myoblasts of the dorsal/lateral musculature, and the posterior spiracle after stage 13, and the cephalic region at stage 17. To further demonstrate the application of our BLI system, we revealed that arm transcriptional activity in embryos was modulated inversely by treatment with ionomycin or 6-bromoindirubin-3-oxime (BIO), an inhibitor and activator of Wnt/β-catenin signaling, respectively. Therefore, our microscopic BLI system is useful for monitoring gene expression in live Drosophila embryos, and for investigating regulatory mechanisms by using chemicals and mutations that might affect expression. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-014-8000-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-41498852014-09-02 Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos Akiyoshi, Ryutaro Kaneuch, Taro Aigaki, Toshiro Suzuki, Hirobumi Anal Bioanal Chem Research Paper We established a method for bioluminescence imaging (BLI) to track real-time gene expression in live Drosophila embryos. We constructed a transgenesis vector containing multiple cloning sites and enhanced green-emitting luciferase (ELuc; Emerald Luc), a brighter and pH-insensitive luciferase for promoter analysis. To evaluate the utility of BLI using an ELuc reporter together with an optimized microscope system, we visualized the expression pattern of armadillo (arm), a member of the Wnt pathway in Drosophila, throughout embryogenesis. We generated transgenic flies carrying the arm:: ELuc fusion gene, and successfully performed BLI continuously for 22 h in the same embryos. Our study showed, for the first time, that arm::Eluc expression was dramatically increased in the anterior midgut rudiment, myoblasts of the dorsal/lateral musculature, and the posterior spiracle after stage 13, and the cephalic region at stage 17. To further demonstrate the application of our BLI system, we revealed that arm transcriptional activity in embryos was modulated inversely by treatment with ionomycin or 6-bromoindirubin-3-oxime (BIO), an inhibitor and activator of Wnt/β-catenin signaling, respectively. Therefore, our microscopic BLI system is useful for monitoring gene expression in live Drosophila embryos, and for investigating regulatory mechanisms by using chemicals and mutations that might affect expression. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-014-8000-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-07-15 2014 /pmc/articles/PMC4149885/ /pubmed/25023969 http://dx.doi.org/10.1007/s00216-014-8000-8 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Paper
Akiyoshi, Ryutaro
Kaneuch, Taro
Aigaki, Toshiro
Suzuki, Hirobumi
Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title_full Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title_fullStr Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title_full_unstemmed Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title_short Bioluminescence imaging to track real-time armadillo promoter activity in live Drosophila embryos
title_sort bioluminescence imaging to track real-time armadillo promoter activity in live drosophila embryos
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149885/
https://www.ncbi.nlm.nih.gov/pubmed/25023969
http://dx.doi.org/10.1007/s00216-014-8000-8
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