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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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). |
format | Online Article Text |
id | pubmed-9619721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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