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Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance
In vitro evolution and whole genome analysis were used to comprehensively identify the genetic determinants of chemical resistance in Saccharomyces cerevisiae. Sequence analysis identified many genes contributing to the resistance phenotype as well as numerous amino acids in potential targets that m...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837787/ https://www.ncbi.nlm.nih.gov/pubmed/35149760 http://dx.doi.org/10.1038/s42003-022-03076-7 |
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author | Ottilie, Sabine Luth, Madeline R. Hellemann, Erich Goldgof, Gregory M. Vigil, Eddy Kumar, Prianka Cheung, Andrea L. Song, Miranda Godinez-Macias, Karla P. Carolino, Krypton Yang, Jennifer Lopez, Gisel Abraham, Matthew Tarsio, Maureen LeBlanc, Emmanuelle Whitesell, Luke Schenken, Jake Gunawan, Felicia Patel, Reysha Smith, Joshua Love, Melissa S. Williams, Roy M. McNamara, Case W. Gerwick, William H. Ideker, Trey Suzuki, Yo Wirth, Dyann F. Lukens, Amanda K. Kane, Patricia M. Cowen, Leah E. Durrant, Jacob D. Winzeler, Elizabeth A. |
author_facet | Ottilie, Sabine Luth, Madeline R. Hellemann, Erich Goldgof, Gregory M. Vigil, Eddy Kumar, Prianka Cheung, Andrea L. Song, Miranda Godinez-Macias, Karla P. Carolino, Krypton Yang, Jennifer Lopez, Gisel Abraham, Matthew Tarsio, Maureen LeBlanc, Emmanuelle Whitesell, Luke Schenken, Jake Gunawan, Felicia Patel, Reysha Smith, Joshua Love, Melissa S. Williams, Roy M. McNamara, Case W. Gerwick, William H. Ideker, Trey Suzuki, Yo Wirth, Dyann F. Lukens, Amanda K. Kane, Patricia M. Cowen, Leah E. Durrant, Jacob D. Winzeler, Elizabeth A. |
author_sort | Ottilie, Sabine |
collection | PubMed |
description | In vitro evolution and whole genome analysis were used to comprehensively identify the genetic determinants of chemical resistance in Saccharomyces cerevisiae. Sequence analysis identified many genes contributing to the resistance phenotype as well as numerous amino acids in potential targets that may play a role in compound binding. Our work shows that compound-target pairs can be conserved across multiple species. The set of 25 most frequently mutated genes was enriched for transcription factors, and for almost 25 percent of the compounds, resistance was mediated by one of 100 independently derived, gain-of-function SNVs found in a 170 amino acid domain in the two Zn(2)C(6) transcription factors YRR1 and YRM1 (p < 1 × 10(−100)). This remarkable enrichment for transcription factors as drug resistance genes highlights their important role in the evolution of antifungal xenobiotic resistance and underscores the challenge to develop antifungal treatments that maintain potency. |
format | Online Article Text |
id | pubmed-8837787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88377872022-03-02 Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance Ottilie, Sabine Luth, Madeline R. Hellemann, Erich Goldgof, Gregory M. Vigil, Eddy Kumar, Prianka Cheung, Andrea L. Song, Miranda Godinez-Macias, Karla P. Carolino, Krypton Yang, Jennifer Lopez, Gisel Abraham, Matthew Tarsio, Maureen LeBlanc, Emmanuelle Whitesell, Luke Schenken, Jake Gunawan, Felicia Patel, Reysha Smith, Joshua Love, Melissa S. Williams, Roy M. McNamara, Case W. Gerwick, William H. Ideker, Trey Suzuki, Yo Wirth, Dyann F. Lukens, Amanda K. Kane, Patricia M. Cowen, Leah E. Durrant, Jacob D. Winzeler, Elizabeth A. Commun Biol Article In vitro evolution and whole genome analysis were used to comprehensively identify the genetic determinants of chemical resistance in Saccharomyces cerevisiae. Sequence analysis identified many genes contributing to the resistance phenotype as well as numerous amino acids in potential targets that may play a role in compound binding. Our work shows that compound-target pairs can be conserved across multiple species. The set of 25 most frequently mutated genes was enriched for transcription factors, and for almost 25 percent of the compounds, resistance was mediated by one of 100 independently derived, gain-of-function SNVs found in a 170 amino acid domain in the two Zn(2)C(6) transcription factors YRR1 and YRM1 (p < 1 × 10(−100)). This remarkable enrichment for transcription factors as drug resistance genes highlights their important role in the evolution of antifungal xenobiotic resistance and underscores the challenge to develop antifungal treatments that maintain potency. Nature Publishing Group UK 2022-02-11 /pmc/articles/PMC8837787/ /pubmed/35149760 http://dx.doi.org/10.1038/s42003-022-03076-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ottilie, Sabine Luth, Madeline R. Hellemann, Erich Goldgof, Gregory M. Vigil, Eddy Kumar, Prianka Cheung, Andrea L. Song, Miranda Godinez-Macias, Karla P. Carolino, Krypton Yang, Jennifer Lopez, Gisel Abraham, Matthew Tarsio, Maureen LeBlanc, Emmanuelle Whitesell, Luke Schenken, Jake Gunawan, Felicia Patel, Reysha Smith, Joshua Love, Melissa S. Williams, Roy M. McNamara, Case W. Gerwick, William H. Ideker, Trey Suzuki, Yo Wirth, Dyann F. Lukens, Amanda K. Kane, Patricia M. Cowen, Leah E. Durrant, Jacob D. Winzeler, Elizabeth A. Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title | Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title_full | Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title_fullStr | Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title_full_unstemmed | Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title_short | Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
title_sort | adaptive laboratory evolution in s. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837787/ https://www.ncbi.nlm.nih.gov/pubmed/35149760 http://dx.doi.org/10.1038/s42003-022-03076-7 |
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