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Identification of novel arsenic resistance genes in yeast

Arsenic is a toxic metalloid that affects human health by causing numerous diseases and by being used in the treatment of acute promyelocytic leukemia. Saccharomyces cerevisiae (budding yeast) has been extensively utilized to elucidate the molecular mechanisms underlying arsenic toxicity and resista...

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Autores principales: Isik, Esin, Balkan, Çiğdem, Karl, Vivien, Karakaya, Hüseyin Çağlar, Hua, Sansan, Rauch, Sebastien, Tamás, Markus J., Koc, Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055376/
https://www.ncbi.nlm.nih.gov/pubmed/35765185
http://dx.doi.org/10.1002/mbo3.1284
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author Isik, Esin
Balkan, Çiğdem
Karl, Vivien
Karakaya, Hüseyin Çağlar
Hua, Sansan
Rauch, Sebastien
Tamás, Markus J.
Koc, Ahmet
author_facet Isik, Esin
Balkan, Çiğdem
Karl, Vivien
Karakaya, Hüseyin Çağlar
Hua, Sansan
Rauch, Sebastien
Tamás, Markus J.
Koc, Ahmet
author_sort Isik, Esin
collection PubMed
description Arsenic is a toxic metalloid that affects human health by causing numerous diseases and by being used in the treatment of acute promyelocytic leukemia. Saccharomyces cerevisiae (budding yeast) has been extensively utilized to elucidate the molecular mechanisms underlying arsenic toxicity and resistance in eukaryotes. In this study, we applied a genomic DNA overexpression strategy to identify yeast genes that provide arsenic resistance in wild‐type and arsenic‐sensitive S. cerevisiae cells. In addition to known arsenic‐related genes, our genetic screen revealed novel genes, including PHO86, VBA3, UGP1, and TUL1, whose overexpression conferred resistance. To gain insights into possible resistance mechanisms, we addressed the contribution of these genes to cell growth, intracellular arsenic, and protein aggregation during arsenate exposure. Overexpression of PHO86 resulted in higher cellular arsenic levels but no additional effect on protein aggregation, indicating that these cells efficiently protect their intracellular environment. VBA3 overexpression caused resistance despite higher intracellular arsenic and protein aggregation levels. Overexpression of UGP1 led to lower intracellular arsenic and protein aggregation levels while TUL1 overexpression had no impact on intracellular arsenic or protein aggregation levels. Thus, the identified genes appear to confer arsenic resistance through distinct mechanisms but the molecular details remain to be elucidated.
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spelling pubmed-90553762022-05-03 Identification of novel arsenic resistance genes in yeast Isik, Esin Balkan, Çiğdem Karl, Vivien Karakaya, Hüseyin Çağlar Hua, Sansan Rauch, Sebastien Tamás, Markus J. Koc, Ahmet Microbiologyopen Original Articles Arsenic is a toxic metalloid that affects human health by causing numerous diseases and by being used in the treatment of acute promyelocytic leukemia. Saccharomyces cerevisiae (budding yeast) has been extensively utilized to elucidate the molecular mechanisms underlying arsenic toxicity and resistance in eukaryotes. In this study, we applied a genomic DNA overexpression strategy to identify yeast genes that provide arsenic resistance in wild‐type and arsenic‐sensitive S. cerevisiae cells. In addition to known arsenic‐related genes, our genetic screen revealed novel genes, including PHO86, VBA3, UGP1, and TUL1, whose overexpression conferred resistance. To gain insights into possible resistance mechanisms, we addressed the contribution of these genes to cell growth, intracellular arsenic, and protein aggregation during arsenate exposure. Overexpression of PHO86 resulted in higher cellular arsenic levels but no additional effect on protein aggregation, indicating that these cells efficiently protect their intracellular environment. VBA3 overexpression caused resistance despite higher intracellular arsenic and protein aggregation levels. Overexpression of UGP1 led to lower intracellular arsenic and protein aggregation levels while TUL1 overexpression had no impact on intracellular arsenic or protein aggregation levels. Thus, the identified genes appear to confer arsenic resistance through distinct mechanisms but the molecular details remain to be elucidated. John Wiley and Sons Inc. 2022-04-30 /pmc/articles/PMC9055376/ /pubmed/35765185 http://dx.doi.org/10.1002/mbo3.1284 Text en © 2022 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Isik, Esin
Balkan, Çiğdem
Karl, Vivien
Karakaya, Hüseyin Çağlar
Hua, Sansan
Rauch, Sebastien
Tamás, Markus J.
Koc, Ahmet
Identification of novel arsenic resistance genes in yeast
title Identification of novel arsenic resistance genes in yeast
title_full Identification of novel arsenic resistance genes in yeast
title_fullStr Identification of novel arsenic resistance genes in yeast
title_full_unstemmed Identification of novel arsenic resistance genes in yeast
title_short Identification of novel arsenic resistance genes in yeast
title_sort identification of novel arsenic resistance genes in yeast
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055376/
https://www.ncbi.nlm.nih.gov/pubmed/35765185
http://dx.doi.org/10.1002/mbo3.1284
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