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Functional mapping of yeast genomes by saturated transposition
Yeast is a powerful model for systems genetics. We present a versatile, time- and labor-efficient method to functionally explore the Saccharomyces cerevisiae genome using saturated transposon mutagenesis coupled to high-throughput sequencing. SAturated Transposon Analysis in Yeast (SATAY) allows one...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466422/ https://www.ncbi.nlm.nih.gov/pubmed/28481201 http://dx.doi.org/10.7554/eLife.23570 |
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author | Michel, Agnès H Hatakeyama, Riko Kimmig, Philipp Arter, Meret Peter, Matthias Matos, Joao De Virgilio, Claudio Kornmann, Benoît |
author_facet | Michel, Agnès H Hatakeyama, Riko Kimmig, Philipp Arter, Meret Peter, Matthias Matos, Joao De Virgilio, Claudio Kornmann, Benoît |
author_sort | Michel, Agnès H |
collection | PubMed |
description | Yeast is a powerful model for systems genetics. We present a versatile, time- and labor-efficient method to functionally explore the Saccharomyces cerevisiae genome using saturated transposon mutagenesis coupled to high-throughput sequencing. SAturated Transposon Analysis in Yeast (SATAY) allows one-step mapping of all genetic loci in which transposons can insert without disrupting essential functions. SATAY is particularly suited to discover loci important for growth under various conditions. SATAY (1) reveals positive and negative genetic interactions in single and multiple mutant strains, (2) can identify drug targets, (3) detects not only essential genes, but also essential protein domains, (4) generates both null and other informative alleles. In a SATAY screen for rapamycin-resistant mutants, we identify Pib2 (PhosphoInositide-Binding 2) as a master regulator of TORC1. We describe two antagonistic TORC1-activating and -inhibiting activities located on opposite ends of Pib2. Thus, SATAY allows to easily explore the yeast genome at unprecedented resolution and throughput. DOI: http://dx.doi.org/10.7554/eLife.23570.001 |
format | Online Article Text |
id | pubmed-5466422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54664222017-06-12 Functional mapping of yeast genomes by saturated transposition Michel, Agnès H Hatakeyama, Riko Kimmig, Philipp Arter, Meret Peter, Matthias Matos, Joao De Virgilio, Claudio Kornmann, Benoît eLife Cell Biology Yeast is a powerful model for systems genetics. We present a versatile, time- and labor-efficient method to functionally explore the Saccharomyces cerevisiae genome using saturated transposon mutagenesis coupled to high-throughput sequencing. SAturated Transposon Analysis in Yeast (SATAY) allows one-step mapping of all genetic loci in which transposons can insert without disrupting essential functions. SATAY is particularly suited to discover loci important for growth under various conditions. SATAY (1) reveals positive and negative genetic interactions in single and multiple mutant strains, (2) can identify drug targets, (3) detects not only essential genes, but also essential protein domains, (4) generates both null and other informative alleles. In a SATAY screen for rapamycin-resistant mutants, we identify Pib2 (PhosphoInositide-Binding 2) as a master regulator of TORC1. We describe two antagonistic TORC1-activating and -inhibiting activities located on opposite ends of Pib2. Thus, SATAY allows to easily explore the yeast genome at unprecedented resolution and throughput. DOI: http://dx.doi.org/10.7554/eLife.23570.001 eLife Sciences Publications, Ltd 2017-05-08 /pmc/articles/PMC5466422/ /pubmed/28481201 http://dx.doi.org/10.7554/eLife.23570 Text en © 2017, Michel et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Michel, Agnès H Hatakeyama, Riko Kimmig, Philipp Arter, Meret Peter, Matthias Matos, Joao De Virgilio, Claudio Kornmann, Benoît Functional mapping of yeast genomes by saturated transposition |
title | Functional mapping of yeast genomes by saturated transposition |
title_full | Functional mapping of yeast genomes by saturated transposition |
title_fullStr | Functional mapping of yeast genomes by saturated transposition |
title_full_unstemmed | Functional mapping of yeast genomes by saturated transposition |
title_short | Functional mapping of yeast genomes by saturated transposition |
title_sort | functional mapping of yeast genomes by saturated transposition |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466422/ https://www.ncbi.nlm.nih.gov/pubmed/28481201 http://dx.doi.org/10.7554/eLife.23570 |
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