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Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae

BACKGROUND: Arsenic and cadmium are widely distributed in nature and pose serious threats to the environment and human health. Exposure to these nonessential toxic metals may result in a variety of human diseases including cancer. However, arsenic and cadmium toxicity targets and the cellular system...

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Autores principales: Thorsen, Michael, Perrone, Gabriel G, Kristiansson, Erik, Traini, Mathew, Ye, Tian, Dawes, Ian W, Nerman, Olle, Tamás, Markus J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660369/
https://www.ncbi.nlm.nih.gov/pubmed/19284616
http://dx.doi.org/10.1186/1471-2164-10-105
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author Thorsen, Michael
Perrone, Gabriel G
Kristiansson, Erik
Traini, Mathew
Ye, Tian
Dawes, Ian W
Nerman, Olle
Tamás, Markus J
author_facet Thorsen, Michael
Perrone, Gabriel G
Kristiansson, Erik
Traini, Mathew
Ye, Tian
Dawes, Ian W
Nerman, Olle
Tamás, Markus J
author_sort Thorsen, Michael
collection PubMed
description BACKGROUND: Arsenic and cadmium are widely distributed in nature and pose serious threats to the environment and human health. Exposure to these nonessential toxic metals may result in a variety of human diseases including cancer. However, arsenic and cadmium toxicity targets and the cellular systems contributing to tolerance acquisition are not fully known. RESULTS: To gain insight into metal action and cellular tolerance mechanisms, we carried out genome-wide screening of the Saccharomyces cerevisiae haploid and homozygous diploid deletion mutant collections and scored for reduced growth in the presence of arsenite or cadmium. Processes found to be required for tolerance to both metals included sulphur and glutathione biosynthesis, environmental sensing, mRNA synthesis and transcription, and vacuolar/endosomal transport and sorting. We also identified metal-specific defence processes. Arsenite-specific defence functions were related to cell cycle regulation, lipid and fatty acid metabolism, mitochondrial biogenesis, and the cytoskeleton whereas cadmium-specific defence functions were mainly related to sugar/carbohydrate metabolism, and metal-ion homeostasis and transport. Molecular evidence indicated that the cytoskeleton is targeted by arsenite and that phosphorylation of the Snf1p kinase is required for cadmium tolerance. CONCLUSION: This study has pin-pointed core functions that protect cells from arsenite and cadmium toxicity. It also emphasizes the existence of both common and specific defence systems. Since many of the yeast genes that confer tolerance to these agents have homologues in humans, similar biological processes may act in yeast and humans to prevent metal toxicity and carcinogenesis.
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spelling pubmed-26603692009-03-25 Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae Thorsen, Michael Perrone, Gabriel G Kristiansson, Erik Traini, Mathew Ye, Tian Dawes, Ian W Nerman, Olle Tamás, Markus J BMC Genomics Research Article BACKGROUND: Arsenic and cadmium are widely distributed in nature and pose serious threats to the environment and human health. Exposure to these nonessential toxic metals may result in a variety of human diseases including cancer. However, arsenic and cadmium toxicity targets and the cellular systems contributing to tolerance acquisition are not fully known. RESULTS: To gain insight into metal action and cellular tolerance mechanisms, we carried out genome-wide screening of the Saccharomyces cerevisiae haploid and homozygous diploid deletion mutant collections and scored for reduced growth in the presence of arsenite or cadmium. Processes found to be required for tolerance to both metals included sulphur and glutathione biosynthesis, environmental sensing, mRNA synthesis and transcription, and vacuolar/endosomal transport and sorting. We also identified metal-specific defence processes. Arsenite-specific defence functions were related to cell cycle regulation, lipid and fatty acid metabolism, mitochondrial biogenesis, and the cytoskeleton whereas cadmium-specific defence functions were mainly related to sugar/carbohydrate metabolism, and metal-ion homeostasis and transport. Molecular evidence indicated that the cytoskeleton is targeted by arsenite and that phosphorylation of the Snf1p kinase is required for cadmium tolerance. CONCLUSION: This study has pin-pointed core functions that protect cells from arsenite and cadmium toxicity. It also emphasizes the existence of both common and specific defence systems. Since many of the yeast genes that confer tolerance to these agents have homologues in humans, similar biological processes may act in yeast and humans to prevent metal toxicity and carcinogenesis. BioMed Central 2009-03-12 /pmc/articles/PMC2660369/ /pubmed/19284616 http://dx.doi.org/10.1186/1471-2164-10-105 Text en Copyright © 2009 Thorsen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Thorsen, Michael
Perrone, Gabriel G
Kristiansson, Erik
Traini, Mathew
Ye, Tian
Dawes, Ian W
Nerman, Olle
Tamás, Markus J
Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title_full Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title_fullStr Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title_full_unstemmed Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title_short Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae
title_sort genetic basis of arsenite and cadmium tolerance in saccharomyces cerevisiae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660369/
https://www.ncbi.nlm.nih.gov/pubmed/19284616
http://dx.doi.org/10.1186/1471-2164-10-105
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