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Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae

Random spore analysis (RSA) is a classic method in yeast genetics that allows high-throughput purification of recombinant haploid spores following specific crosses. RSA typically involves a number of steps to induce sporulation, purge vegetative cells that fail to sporulate, and disrupt the ascus wa...

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Autores principales: Burke, Molly K., McHugh, Kaitlin M., Kutch, Ian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759604/
https://www.ncbi.nlm.nih.gov/pubmed/33362858
http://dx.doi.org/10.3389/fgene.2020.597482
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author Burke, Molly K.
McHugh, Kaitlin M.
Kutch, Ian C.
author_facet Burke, Molly K.
McHugh, Kaitlin M.
Kutch, Ian C.
author_sort Burke, Molly K.
collection PubMed
description Random spore analysis (RSA) is a classic method in yeast genetics that allows high-throughput purification of recombinant haploid spores following specific crosses. RSA typically involves a number of steps to induce sporulation, purge vegetative cells that fail to sporulate, and disrupt the ascus walls of sporulated cells to release haploid spores. These steps generally require expensive chemicals and/or enzymes that kill diploid cells but have few effects on spores. In the fission yeast Schizosaccharomcyes pombe, heat shock has been reported as an effective addition to RSA protocols, but to our knowledge heat shock has not been used for this purpose in the budding yeast Saccharomyces cerevisiae. Here, we evaluate the effects of heat shock on vegetative and sporulated cultures of four diverse yeast strains: a European wine strain (DBVPG6765), a Japanese sake strain (Y12), a West African palm wine strain (DBVPG6044) and a North American strain isolated from the soil beneath an oak tree (YPS128). We characterize this phenotype under multiple combinations of temperature and incubation time, and find specific conditions that lead to the exclusion of vegetative cells and an enrichment in spores, which differ by strain. We also collected genome sequence data from a recombinant population that experienced multiple rounds of RSA, including one round with a heat shock treatment. These data suggest that when incorporated into an RSA protocol, heat shock leads to increased genetic diversity among the cells that survive and mate. Ultimately, our work provides evidence that short heat treatments can improve existing RSA protocols, though in a strain-specific manner. This result informs applications of high-throughput RSA protocols, such as QTL mapping and experimental evolution research.
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spelling pubmed-77596042020-12-26 Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae Burke, Molly K. McHugh, Kaitlin M. Kutch, Ian C. Front Genet Genetics Random spore analysis (RSA) is a classic method in yeast genetics that allows high-throughput purification of recombinant haploid spores following specific crosses. RSA typically involves a number of steps to induce sporulation, purge vegetative cells that fail to sporulate, and disrupt the ascus walls of sporulated cells to release haploid spores. These steps generally require expensive chemicals and/or enzymes that kill diploid cells but have few effects on spores. In the fission yeast Schizosaccharomcyes pombe, heat shock has been reported as an effective addition to RSA protocols, but to our knowledge heat shock has not been used for this purpose in the budding yeast Saccharomyces cerevisiae. Here, we evaluate the effects of heat shock on vegetative and sporulated cultures of four diverse yeast strains: a European wine strain (DBVPG6765), a Japanese sake strain (Y12), a West African palm wine strain (DBVPG6044) and a North American strain isolated from the soil beneath an oak tree (YPS128). We characterize this phenotype under multiple combinations of temperature and incubation time, and find specific conditions that lead to the exclusion of vegetative cells and an enrichment in spores, which differ by strain. We also collected genome sequence data from a recombinant population that experienced multiple rounds of RSA, including one round with a heat shock treatment. These data suggest that when incorporated into an RSA protocol, heat shock leads to increased genetic diversity among the cells that survive and mate. Ultimately, our work provides evidence that short heat treatments can improve existing RSA protocols, though in a strain-specific manner. This result informs applications of high-throughput RSA protocols, such as QTL mapping and experimental evolution research. Frontiers Media S.A. 2020-12-11 /pmc/articles/PMC7759604/ /pubmed/33362858 http://dx.doi.org/10.3389/fgene.2020.597482 Text en Copyright © 2020 Burke, McHugh and Kutch. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Burke, Molly K.
McHugh, Kaitlin M.
Kutch, Ian C.
Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title_full Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title_fullStr Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title_full_unstemmed Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title_short Heat Shock Improves Random Spore Analysis in Diverse Strains of Saccharomyces cerevisiae
title_sort heat shock improves random spore analysis in diverse strains of saccharomyces cerevisiae
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759604/
https://www.ncbi.nlm.nih.gov/pubmed/33362858
http://dx.doi.org/10.3389/fgene.2020.597482
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