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Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms
Due to epistasis, the same mutation can have drastically different phenotypic consequences in different individuals. This phenomenon is pertinent to precision medicine as well as antimicrobial drug development, but its general characteristics are largely unknown. We approach this question by genome-...
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/PMC8938418/ https://www.ncbi.nlm.nih.gov/pubmed/35314699 http://dx.doi.org/10.1038/s41467-022-29228-1 |
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author | Chen, Piaopiao Michel, Agnès H. Zhang, Jianzhi |
author_facet | Chen, Piaopiao Michel, Agnès H. Zhang, Jianzhi |
author_sort | Chen, Piaopiao |
collection | PubMed |
description | Due to epistasis, the same mutation can have drastically different phenotypic consequences in different individuals. This phenomenon is pertinent to precision medicine as well as antimicrobial drug development, but its general characteristics are largely unknown. We approach this question by genome-wide assessment of gene essentiality polymorphism in 16 Saccharomyces cerevisiae strains using transposon insertional mutagenesis. Essentiality polymorphism is observed for 9.8% of genes, most of which have had repeated essentiality switches in evolution. Genes exhibiting essentiality polymorphism lean toward having intermediate numbers of genetic and protein interactions. Gene essentiality changes tend to occur concordantly among components of the same protein complex or metabolic pathway and among a group of over 100 mitochondrial proteins, revealing molecular machines or functional modules as units of gene essentiality variation. Most essential genes tolerate transposon insertions consistently among strains in one or more coding segments, delineating nonessential regions within essential genes. |
format | Online Article Text |
id | pubmed-8938418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89384182022-04-08 Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms Chen, Piaopiao Michel, Agnès H. Zhang, Jianzhi Nat Commun Article Due to epistasis, the same mutation can have drastically different phenotypic consequences in different individuals. This phenomenon is pertinent to precision medicine as well as antimicrobial drug development, but its general characteristics are largely unknown. We approach this question by genome-wide assessment of gene essentiality polymorphism in 16 Saccharomyces cerevisiae strains using transposon insertional mutagenesis. Essentiality polymorphism is observed for 9.8% of genes, most of which have had repeated essentiality switches in evolution. Genes exhibiting essentiality polymorphism lean toward having intermediate numbers of genetic and protein interactions. Gene essentiality changes tend to occur concordantly among components of the same protein complex or metabolic pathway and among a group of over 100 mitochondrial proteins, revealing molecular machines or functional modules as units of gene essentiality variation. Most essential genes tolerate transposon insertions consistently among strains in one or more coding segments, delineating nonessential regions within essential genes. Nature Publishing Group UK 2022-03-21 /pmc/articles/PMC8938418/ /pubmed/35314699 http://dx.doi.org/10.1038/s41467-022-29228-1 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 Chen, Piaopiao Michel, Agnès H. Zhang, Jianzhi Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title | Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title_full | Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title_fullStr | Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title_full_unstemmed | Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title_short | Transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
title_sort | transposon insertional mutagenesis of diverse yeast strains suggests coordinated gene essentiality polymorphisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938418/ https://www.ncbi.nlm.nih.gov/pubmed/35314699 http://dx.doi.org/10.1038/s41467-022-29228-1 |
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