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SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae

Copper tolerance and SO(2) tolerance are two well-studied phenotypic traits of Saccharomyces cerevisiae. The genetic bases of these traits are the allelic expansion at the CUP1 locus and reciprocal translocation at the SSU1 locus, respectively. Previous work identified a negative association between...

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Autores principales: Onetto, Cristobal A., Kutyna, Dariusz R., Kolouchova, Radka, McCarthy, Jane, Borneman, Anthony R., Schmidt, Simon A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081759/
https://www.ncbi.nlm.nih.gov/pubmed/36976798
http://dx.doi.org/10.1371/journal.pgen.1010692
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author Onetto, Cristobal A.
Kutyna, Dariusz R.
Kolouchova, Radka
McCarthy, Jane
Borneman, Anthony R.
Schmidt, Simon A.
author_facet Onetto, Cristobal A.
Kutyna, Dariusz R.
Kolouchova, Radka
McCarthy, Jane
Borneman, Anthony R.
Schmidt, Simon A.
author_sort Onetto, Cristobal A.
collection PubMed
description Copper tolerance and SO(2) tolerance are two well-studied phenotypic traits of Saccharomyces cerevisiae. The genetic bases of these traits are the allelic expansion at the CUP1 locus and reciprocal translocation at the SSU1 locus, respectively. Previous work identified a negative association between SO(2) and copper tolerance in S. cerevisiae wine yeasts. Here we probe the relationship between SO(2) and copper tolerance and show that an increase in CUP1 copy number does not always impart copper tolerance in S. cerevisiae wine yeast. Bulk-segregant QTL analysis was used to identify variance at SSU1 as a causative factor in copper sensitivity, which was verified by reciprocal hemizygosity analysis in a strain carrying 20 copies of CUP1. Transcriptional and proteomic analysis demonstrated that SSU1 over-expression did not suppress CUP1 transcription or constrain protein production and provided evidence that SSU1 over-expression induced sulfur limitation during exposure to copper. Finally, an SSU1 over-expressing strain exhibited increased sensitivity to moderately elevated copper concentrations in sulfur-limited medium, demonstrating that SSU1 over-expression burdens the sulfate assimilation pathway. Over-expression of MET 3/14/16, genes upstream of H(2)S production in the sulfate assimilation pathway increased the production of SO(2) and H(2)S but did not improve copper sensitivity in an SSU1 over-expressing background. We conclude that copper and SO(2) tolerance are conditional traits in S. cerevisiae and provide evidence of the metabolic basis for their mutual exclusivity. These findings suggest an evolutionary driver for the extreme amplification of CUP1 observed in some yeasts.
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spelling pubmed-100817592023-04-08 SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae Onetto, Cristobal A. Kutyna, Dariusz R. Kolouchova, Radka McCarthy, Jane Borneman, Anthony R. Schmidt, Simon A. PLoS Genet Research Article Copper tolerance and SO(2) tolerance are two well-studied phenotypic traits of Saccharomyces cerevisiae. The genetic bases of these traits are the allelic expansion at the CUP1 locus and reciprocal translocation at the SSU1 locus, respectively. Previous work identified a negative association between SO(2) and copper tolerance in S. cerevisiae wine yeasts. Here we probe the relationship between SO(2) and copper tolerance and show that an increase in CUP1 copy number does not always impart copper tolerance in S. cerevisiae wine yeast. Bulk-segregant QTL analysis was used to identify variance at SSU1 as a causative factor in copper sensitivity, which was verified by reciprocal hemizygosity analysis in a strain carrying 20 copies of CUP1. Transcriptional and proteomic analysis demonstrated that SSU1 over-expression did not suppress CUP1 transcription or constrain protein production and provided evidence that SSU1 over-expression induced sulfur limitation during exposure to copper. Finally, an SSU1 over-expressing strain exhibited increased sensitivity to moderately elevated copper concentrations in sulfur-limited medium, demonstrating that SSU1 over-expression burdens the sulfate assimilation pathway. Over-expression of MET 3/14/16, genes upstream of H(2)S production in the sulfate assimilation pathway increased the production of SO(2) and H(2)S but did not improve copper sensitivity in an SSU1 over-expressing background. We conclude that copper and SO(2) tolerance are conditional traits in S. cerevisiae and provide evidence of the metabolic basis for their mutual exclusivity. These findings suggest an evolutionary driver for the extreme amplification of CUP1 observed in some yeasts. Public Library of Science 2023-03-28 /pmc/articles/PMC10081759/ /pubmed/36976798 http://dx.doi.org/10.1371/journal.pgen.1010692 Text en © 2023 Onetto et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Onetto, Cristobal A.
Kutyna, Dariusz R.
Kolouchova, Radka
McCarthy, Jane
Borneman, Anthony R.
Schmidt, Simon A.
SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title_full SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title_fullStr SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title_full_unstemmed SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title_short SO(2) and copper tolerance exhibit an evolutionary trade-off in Saccharomyces cerevisiae
title_sort so(2) and copper tolerance exhibit an evolutionary trade-off in saccharomyces cerevisiae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081759/
https://www.ncbi.nlm.nih.gov/pubmed/36976798
http://dx.doi.org/10.1371/journal.pgen.1010692
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