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A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila

The Drosophila visual system has been proved to be a powerful genetic model to study eye disease such as retinal degeneration. Here, we describe a genetic method termed “Rh1::GFP ey-flp/hid” that is based on the fluorescence of GFP-tagged major rhodopsin Rh1 in the eyes of living flies and can be us...

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Detalles Bibliográficos
Autores principales: Huang, Yu, Xie, Jun, Wang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684387/
https://www.ncbi.nlm.nih.gov/pubmed/26659849
http://dx.doi.org/10.1371/journal.pone.0144925
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author Huang, Yu
Xie, Jun
Wang, Tao
author_facet Huang, Yu
Xie, Jun
Wang, Tao
author_sort Huang, Yu
collection PubMed
description The Drosophila visual system has been proved to be a powerful genetic model to study eye disease such as retinal degeneration. Here, we describe a genetic method termed “Rh1::GFP ey-flp/hid” that is based on the fluorescence of GFP-tagged major rhodopsin Rh1 in the eyes of living flies and can be used to monitor the integrity of photoreceptor cells. Through combination of this method and ERG recording, we examined a collection of 667 mutants and identified 18 genes that are required for photoreceptor cell maintenance, photoresponse, and rhodopsin synthesis. Our findings demonstrate that this “Rh1::GFP ey-flp/hid” method enables high-throughput F1 genetic screens to rapidly and precisely identify mutations of retinal degeneration.
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spelling pubmed-46843872015-12-31 A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila Huang, Yu Xie, Jun Wang, Tao PLoS One Research Article The Drosophila visual system has been proved to be a powerful genetic model to study eye disease such as retinal degeneration. Here, we describe a genetic method termed “Rh1::GFP ey-flp/hid” that is based on the fluorescence of GFP-tagged major rhodopsin Rh1 in the eyes of living flies and can be used to monitor the integrity of photoreceptor cells. Through combination of this method and ERG recording, we examined a collection of 667 mutants and identified 18 genes that are required for photoreceptor cell maintenance, photoresponse, and rhodopsin synthesis. Our findings demonstrate that this “Rh1::GFP ey-flp/hid” method enables high-throughput F1 genetic screens to rapidly and precisely identify mutations of retinal degeneration. Public Library of Science 2015-12-14 /pmc/articles/PMC4684387/ /pubmed/26659849 http://dx.doi.org/10.1371/journal.pone.0144925 Text en © 2015 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Huang, Yu
Xie, Jun
Wang, Tao
A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title_full A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title_fullStr A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title_full_unstemmed A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title_short A Fluorescence-Based Genetic Screen to Study Retinal Degeneration in Drosophila
title_sort fluorescence-based genetic screen to study retinal degeneration in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684387/
https://www.ncbi.nlm.nih.gov/pubmed/26659849
http://dx.doi.org/10.1371/journal.pone.0144925
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