Genomic analysis of stress response against arsenic in Caenorhabditis elegans.

Arsenic, a known human carcinogen, is widely distributed around the world and found in particularly high concentrations in certain regions including Southwestern US, Eastern Europe, India, China, Taiwan and Mexico. Chronic arsenic poisoning affects millions of people worldwide and is associated with...

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Main Authors: Surasri N Sahu, Jada Lewis, Isha Patel, Serdar Bozdag, Jeong H Lee, Robert Sprando, Hediye Nese Cinar
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3722197?pdf=render
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author Surasri N Sahu
Jada Lewis
Isha Patel
Serdar Bozdag
Jeong H Lee
Robert Sprando
Hediye Nese Cinar
author_facet Surasri N Sahu
Jada Lewis
Isha Patel
Serdar Bozdag
Jeong H Lee
Robert Sprando
Hediye Nese Cinar
author_sort Surasri N Sahu
collection DOAJ
description Arsenic, a known human carcinogen, is widely distributed around the world and found in particularly high concentrations in certain regions including Southwestern US, Eastern Europe, India, China, Taiwan and Mexico. Chronic arsenic poisoning affects millions of people worldwide and is associated with increased risk of many diseases including arthrosclerosis, diabetes and cancer. In this study, we explored genome level global responses to high and low levels of arsenic exposure in Caenorhabditis elegans using Affymetrix expression microarrays. This experimental design allows us to do microarray analysis of dose-response relationships of global gene expression patterns. High dose (0.03%) exposure caused stronger global gene expression changes in comparison with low dose (0.003%) exposure, suggesting a positive dose-response correlation. Biological processes such as oxidative stress, and iron metabolism, which were previously reported to be involved in arsenic toxicity studies using cultured cells, experimental animals, and humans, were found to be affected in C. elegans. We performed genome-wide gene expression comparisons between our microarray data and publicly available C. elegans microarray datasets of cadmium, and sediment exposure samples of German rivers Rhine and Elbe. Bioinformatics analysis of arsenic-responsive regulatory networks were done using FastMEDUSA program. FastMEDUSA analysis identified cancer-related genes, particularly genes associated with leukemia, such as dnj-11, which encodes a protein orthologous to the mammalian ZRF1/MIDA1/MPP11/DNAJC2 family of ribosome-associated molecular chaperones. We analyzed the protective functions of several of the identified genes using RNAi. Our study indicates that C. elegans could be a substitute model to study the mechanism of metal toxicity using high-throughput expression data and bioinformatics tools such as FastMEDUSA.
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spelling doaj.art-3f7e1f9ee0ec4540a11e81af6a8fe2c32022-12-21T18:40:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6643110.1371/journal.pone.0066431Genomic analysis of stress response against arsenic in Caenorhabditis elegans.Surasri N SahuJada LewisIsha PatelSerdar BozdagJeong H LeeRobert SprandoHediye Nese CinarArsenic, a known human carcinogen, is widely distributed around the world and found in particularly high concentrations in certain regions including Southwestern US, Eastern Europe, India, China, Taiwan and Mexico. Chronic arsenic poisoning affects millions of people worldwide and is associated with increased risk of many diseases including arthrosclerosis, diabetes and cancer. In this study, we explored genome level global responses to high and low levels of arsenic exposure in Caenorhabditis elegans using Affymetrix expression microarrays. This experimental design allows us to do microarray analysis of dose-response relationships of global gene expression patterns. High dose (0.03%) exposure caused stronger global gene expression changes in comparison with low dose (0.003%) exposure, suggesting a positive dose-response correlation. Biological processes such as oxidative stress, and iron metabolism, which were previously reported to be involved in arsenic toxicity studies using cultured cells, experimental animals, and humans, were found to be affected in C. elegans. We performed genome-wide gene expression comparisons between our microarray data and publicly available C. elegans microarray datasets of cadmium, and sediment exposure samples of German rivers Rhine and Elbe. Bioinformatics analysis of arsenic-responsive regulatory networks were done using FastMEDUSA program. FastMEDUSA analysis identified cancer-related genes, particularly genes associated with leukemia, such as dnj-11, which encodes a protein orthologous to the mammalian ZRF1/MIDA1/MPP11/DNAJC2 family of ribosome-associated molecular chaperones. We analyzed the protective functions of several of the identified genes using RNAi. Our study indicates that C. elegans could be a substitute model to study the mechanism of metal toxicity using high-throughput expression data and bioinformatics tools such as FastMEDUSA.http://europepmc.org/articles/PMC3722197?pdf=render
spellingShingle Surasri N Sahu
Jada Lewis
Isha Patel
Serdar Bozdag
Jeong H Lee
Robert Sprando
Hediye Nese Cinar
Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
PLoS ONE
title Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
title_full Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
title_fullStr Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
title_full_unstemmed Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
title_short Genomic analysis of stress response against arsenic in Caenorhabditis elegans.
title_sort genomic analysis of stress response against arsenic in caenorhabditis elegans
url http://europepmc.org/articles/PMC3722197?pdf=render
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