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High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae

Simple genetic screens in budding yeast have identified many conserved meiotic regulators. However, the identification of genes involved in specific steps of meiosis may require a more complex genetic screen that allows visualization of meiosis. Here, we describe a high-throughput protocol using flu...

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Detalles Bibliográficos
Autores principales: Gavade, Janardan N., Lacefield, Soni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619721/
https://www.ncbi.nlm.nih.gov/pubmed/36325582
http://dx.doi.org/10.1016/j.xpro.2022.101797
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author Gavade, Janardan N.
Lacefield, Soni
author_facet Gavade, Janardan N.
Lacefield, Soni
author_sort Gavade, Janardan N.
collection PubMed
description Simple genetic screens in budding yeast have identified many conserved meiotic regulators. However, the identification of genes involved in specific steps of meiosis may require a more complex genetic screen that allows visualization of meiosis. Here, we describe a high-throughput protocol using fluorescence microscopy to systematically screen an overexpression library to identify genes involved in meiotic commitment. We also explain how this protocol can be adapted for identifying proteins that function at different stages of meiosis. For complete details on the use and execution of this protocol, please refer to Gavade et al. (2022).
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spelling pubmed-96197212022-11-01 High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae Gavade, Janardan N. Lacefield, Soni STAR Protoc Protocol Simple genetic screens in budding yeast have identified many conserved meiotic regulators. However, the identification of genes involved in specific steps of meiosis may require a more complex genetic screen that allows visualization of meiosis. Here, we describe a high-throughput protocol using fluorescence microscopy to systematically screen an overexpression library to identify genes involved in meiotic commitment. We also explain how this protocol can be adapted for identifying proteins that function at different stages of meiosis. For complete details on the use and execution of this protocol, please refer to Gavade et al. (2022). Elsevier 2022-10-27 /pmc/articles/PMC9619721/ /pubmed/36325582 http://dx.doi.org/10.1016/j.xpro.2022.101797 Text en © 2022 The Authors https://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
Gavade, Janardan N.
Lacefield, Soni
High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title_full High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title_fullStr High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title_full_unstemmed High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title_short High-throughput genetic screening of meiotic commitment using fluorescence microscopy in Saccharomyces cerevisiae
title_sort high-throughput genetic screening of meiotic commitment using fluorescence microscopy in saccharomyces cerevisiae
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619721/
https://www.ncbi.nlm.nih.gov/pubmed/36325582
http://dx.doi.org/10.1016/j.xpro.2022.101797
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