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Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis
Metal pollution has made a significant impact on the earth’s ecosystems and tolerance to metals in a wide variety of species has evolved. Metallothioneins, a group of cysteine-rich metal-ion binding proteins, are known to be a key physiological mechanism in regulating protection against metal toxici...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694099/ https://www.ncbi.nlm.nih.gov/pubmed/31413359 http://dx.doi.org/10.1038/s41598-019-48303-0 |
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author | Paris, Josephine R. Usher, Jane |
author_facet | Paris, Josephine R. Usher, Jane |
author_sort | Paris, Josephine R. |
collection | PubMed |
description | Metal pollution has made a significant impact on the earth’s ecosystems and tolerance to metals in a wide variety of species has evolved. Metallothioneins, a group of cysteine-rich metal-ion binding proteins, are known to be a key physiological mechanism in regulating protection against metal toxicity. Many rivers across the southwest of England are detrimentally affected by metal pollution, but brown trout (Salmo trutta L.) populations are known to reside within them. In this body of work, two isoforms of metallothionein (MetA and MetB) isolated from trout occupying a polluted and a control river are examined. Using synthetic genetic array (SGA) analyses in the model yeast, Saccharomyces cerevisiae, functional genomics is used to explore the role of metallothionein isoforms in driving metal tolerance. By harnessing this experimental system, S. cerevisiae is used to (i) determine the genetic interaction maps of MetA and MetB isoforms; (ii) identify differences between the genetic interactions in both isoforms and (iii) demonstrate that pre-exposure to metals in metal-tolerant trout influences these interactions. By using a functional genomics approach leveraged from the model yeast Saccharomyces cerevisiae, we demonstrate how such approaches could be used in understanding the ecology and evolution of a non-model species. |
format | Online Article Text |
id | pubmed-6694099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66940992019-08-19 Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis Paris, Josephine R. Usher, Jane Sci Rep Article Metal pollution has made a significant impact on the earth’s ecosystems and tolerance to metals in a wide variety of species has evolved. Metallothioneins, a group of cysteine-rich metal-ion binding proteins, are known to be a key physiological mechanism in regulating protection against metal toxicity. Many rivers across the southwest of England are detrimentally affected by metal pollution, but brown trout (Salmo trutta L.) populations are known to reside within them. In this body of work, two isoforms of metallothionein (MetA and MetB) isolated from trout occupying a polluted and a control river are examined. Using synthetic genetic array (SGA) analyses in the model yeast, Saccharomyces cerevisiae, functional genomics is used to explore the role of metallothionein isoforms in driving metal tolerance. By harnessing this experimental system, S. cerevisiae is used to (i) determine the genetic interaction maps of MetA and MetB isoforms; (ii) identify differences between the genetic interactions in both isoforms and (iii) demonstrate that pre-exposure to metals in metal-tolerant trout influences these interactions. By using a functional genomics approach leveraged from the model yeast Saccharomyces cerevisiae, we demonstrate how such approaches could be used in understanding the ecology and evolution of a non-model species. Nature Publishing Group UK 2019-08-14 /pmc/articles/PMC6694099/ /pubmed/31413359 http://dx.doi.org/10.1038/s41598-019-48303-0 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Paris, Josephine R. Usher, Jane Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title | Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title_full | Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title_fullStr | Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title_full_unstemmed | Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title_short | Functional genomic characterization of metallothioneins in brown trout (Salmo trutta L.). using synthetic genetic analysis |
title_sort | functional genomic characterization of metallothioneins in brown trout (salmo trutta l.). using synthetic genetic analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694099/ https://www.ncbi.nlm.nih.gov/pubmed/31413359 http://dx.doi.org/10.1038/s41598-019-48303-0 |
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