A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.

Exposure to toxaphene, an environmentally persistent mixture of chlorinated terpenes previously utilized as an insecticide, has been associated with various cancers and diseases such as amyotrophic lateral sclerosis. Nevertheless, the cellular and molecular mechanisms responsible for these toxic eff...

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Main Authors: Brandon D Gaytán, Alex V Loguinov, Xenia Peñate, Jan-Michael Lerot, Sebastián Chávez, Nancy D Denslow, Chris D Vulpe
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3832591?pdf=render
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spelling doaj-736133a536cf4c0a9fba118fd3bea4632020-11-25T00:42:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e8125310.1371/journal.pone.0081253A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.Brandon D GaytánAlex V LoguinovXenia PeñateJan-Michael LerotSebastián ChávezNancy D DenslowChris D VulpeExposure to toxaphene, an environmentally persistent mixture of chlorinated terpenes previously utilized as an insecticide, has been associated with various cancers and diseases such as amyotrophic lateral sclerosis. Nevertheless, the cellular and molecular mechanisms responsible for these toxic effects have not been established. In this study, we used a functional approach in the model eukaryote Saccharomyces cerevisiae to demonstrate that toxaphene affects yeast mutants defective in (1) processes associated with transcription elongation and (2) nutrient utilization. Synergistic growth defects are observed upon exposure to both toxaphene and the known transcription elongation inhibitor mycophenolic acid (MPA). However, unlike MPA, toxaphene does not deplete nucleotides and additionally has no detectable effect on transcription elongation. Many of the yeast genes identified in this study have human homologs, warranting further investigations into the potentially conserved mechanisms of toxaphene toxicity.http://europepmc.org/articles/PMC3832591?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Brandon D Gaytán
Alex V Loguinov
Xenia Peñate
Jan-Michael Lerot
Sebastián Chávez
Nancy D Denslow
Chris D Vulpe
spellingShingle Brandon D Gaytán
Alex V Loguinov
Xenia Peñate
Jan-Michael Lerot
Sebastián Chávez
Nancy D Denslow
Chris D Vulpe
A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
PLoS ONE
author_facet Brandon D Gaytán
Alex V Loguinov
Xenia Peñate
Jan-Michael Lerot
Sebastián Chávez
Nancy D Denslow
Chris D Vulpe
author_sort Brandon D Gaytán
title A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
title_short A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
title_full A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
title_fullStr A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
title_full_unstemmed A genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
title_sort genome-wide screen identifies yeast genes required for tolerance to technical toxaphene, an organochlorinated pesticide mixture.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Exposure to toxaphene, an environmentally persistent mixture of chlorinated terpenes previously utilized as an insecticide, has been associated with various cancers and diseases such as amyotrophic lateral sclerosis. Nevertheless, the cellular and molecular mechanisms responsible for these toxic effects have not been established. In this study, we used a functional approach in the model eukaryote Saccharomyces cerevisiae to demonstrate that toxaphene affects yeast mutants defective in (1) processes associated with transcription elongation and (2) nutrient utilization. Synergistic growth defects are observed upon exposure to both toxaphene and the known transcription elongation inhibitor mycophenolic acid (MPA). However, unlike MPA, toxaphene does not deplete nucleotides and additionally has no detectable effect on transcription elongation. Many of the yeast genes identified in this study have human homologs, warranting further investigations into the potentially conserved mechanisms of toxaphene toxicity.
url http://europepmc.org/articles/PMC3832591?pdf=render
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