A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye

microRNAs (miRNAs) are a broad class of ~22 nucleotide regulatory RNA, which collectively have broad effects on the transcriptome and are involved in diverse biology, from development and adult physiology, and from homeostasis to disease and pathology. We investigated the effects of systematically e...

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Main Authors: Fernando Bejarano, Eric C. Lai
Format: Article
Language:English
Published: Elsevier 2021-06-01
Series:Data in Brief
Subjects:
Eye
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340921003218
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spelling doaj-703b33aa3ec5490ab292f5b70356aa6b2021-06-27T04:38:03ZengElsevierData in Brief2352-34092021-06-0136107037A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eyeFernando Bejarano0Eric C. Lai1Developmental Biology Program, Sloan Kettering Institute, 1275 York Ave, Box 252, New York, NY 10065, USACorresponding author.; Developmental Biology Program, Sloan Kettering Institute, 1275 York Ave, Box 252, New York, NY 10065, USAmicroRNAs (miRNAs) are a broad class of ~22 nucleotide regulatory RNA, which collectively have broad effects on the transcriptome and are involved in diverse biology, from development and adult physiology, and from homeostasis to disease and pathology. We investigated the effects of systematically expressing microRNAs (miRNAs) during the development of the Drosophila compound eye using the GMR-Gal4 driver. The objective was to determine what fraction of miRNAs were capable of inducing aberrant morphology that was easily and reproducibly scored by visual inspection under a dissecting microscope. We assayed multiple independent insertions of 166 miRNA transgenes (536 lines), comprising solo miRNAs, miRNA operons and individual constituent miRNAs from operons. We find a substantial number reproducibly altered normal eye development and a smaller number induced lethality in most or all progeny. We provide the comprehensive results of this screen, documenting numerous miRNA transgenes that interfered with normal eye development when activated using GMR-Gal4. These data can be mined by the Drosophila community to query the in vivo effects of any individual miRNA of interest in the eye, as well as utilized as a foundation for more complex genetic perturbations that involve miRNA misexpression in the eye.http://www.sciencedirect.com/science/article/pii/S2352340921003218DrosophilaEyemicroRNAGenetic screen
collection DOAJ
language English
format Article
sources DOAJ
author Fernando Bejarano
Eric C. Lai
spellingShingle Fernando Bejarano
Eric C. Lai
A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
Data in Brief
Drosophila
Eye
microRNA
Genetic screen
author_facet Fernando Bejarano
Eric C. Lai
author_sort Fernando Bejarano
title A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
title_short A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
title_full A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
title_fullStr A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
title_full_unstemmed A comprehensive dataset of microRNA misexpression phenotypes in the Drosophila eye
title_sort comprehensive dataset of microrna misexpression phenotypes in the drosophila eye
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2021-06-01
description microRNAs (miRNAs) are a broad class of ~22 nucleotide regulatory RNA, which collectively have broad effects on the transcriptome and are involved in diverse biology, from development and adult physiology, and from homeostasis to disease and pathology. We investigated the effects of systematically expressing microRNAs (miRNAs) during the development of the Drosophila compound eye using the GMR-Gal4 driver. The objective was to determine what fraction of miRNAs were capable of inducing aberrant morphology that was easily and reproducibly scored by visual inspection under a dissecting microscope. We assayed multiple independent insertions of 166 miRNA transgenes (536 lines), comprising solo miRNAs, miRNA operons and individual constituent miRNAs from operons. We find a substantial number reproducibly altered normal eye development and a smaller number induced lethality in most or all progeny. We provide the comprehensive results of this screen, documenting numerous miRNA transgenes that interfered with normal eye development when activated using GMR-Gal4. These data can be mined by the Drosophila community to query the in vivo effects of any individual miRNA of interest in the eye, as well as utilized as a foundation for more complex genetic perturbations that involve miRNA misexpression in the eye.
topic Drosophila
Eye
microRNA
Genetic screen
url http://www.sciencedirect.com/science/article/pii/S2352340921003218
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