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Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc

All organisms are confronted with external variations in trace element abundance. To elucidate the mechanisms that maintain metal homeostasis and protect against heavy metal stress, we have determined the transcriptome responses in Drosophila to sublethal doses of cadmium, zinc, copper, as well as t...

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Autores principales: Yepiskoposyan, Hasmik, Egli, Dieter, Fergestad, Tim, Selvaraj, Anand, Treiber, Carina, Multhaup, Gerd, Georgiev, Oleg, Schaffner, Walter
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635269/
https://www.ncbi.nlm.nih.gov/pubmed/16973896
http://dx.doi.org/10.1093/nar/gkl606
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author Yepiskoposyan, Hasmik
Egli, Dieter
Fergestad, Tim
Selvaraj, Anand
Treiber, Carina
Multhaup, Gerd
Georgiev, Oleg
Schaffner, Walter
author_facet Yepiskoposyan, Hasmik
Egli, Dieter
Fergestad, Tim
Selvaraj, Anand
Treiber, Carina
Multhaup, Gerd
Georgiev, Oleg
Schaffner, Walter
author_sort Yepiskoposyan, Hasmik
collection PubMed
description All organisms are confronted with external variations in trace element abundance. To elucidate the mechanisms that maintain metal homeostasis and protect against heavy metal stress, we have determined the transcriptome responses in Drosophila to sublethal doses of cadmium, zinc, copper, as well as to copper depletion. Furthermore, we analyzed the transcriptome of a metal-responsive transcription factor (MTF-1) null mutant. The gene family encoding metallothioneins, and the ABC transporter CG10505 that encodes a homolog of ‘yeast cadmium factor’ were induced by all three metals. Zinc and cadmium responses have similar features: genes upregulated by both metals include those for glutathione S-transferases GstD2 and GstD5, and for zinc transporter-like proteins designated ZnT35C and ZnT63C. Several of the metal-induced genes that emerged in our study are regulated by the transcription factor MTF-1. mRNA studies in MTF-1 overexpressing or null mutant flies and in silico search for metal response elements (binding sites for MTF-1) confirmed novel MTF-1 regulated genes such as ferritins, the ABC transporter CG10505 and the zinc transporter ZnT35C. The latter was analyzed in most detail; biochemical and genetic approaches, including targeted mutation, indicate that ZnT35C is involved in cellular and organismal zinc efflux and plays a major role in zinc detoxification.
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spelling pubmed-16352692006-11-29 Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc Yepiskoposyan, Hasmik Egli, Dieter Fergestad, Tim Selvaraj, Anand Treiber, Carina Multhaup, Gerd Georgiev, Oleg Schaffner, Walter Nucleic Acids Res Genomics All organisms are confronted with external variations in trace element abundance. To elucidate the mechanisms that maintain metal homeostasis and protect against heavy metal stress, we have determined the transcriptome responses in Drosophila to sublethal doses of cadmium, zinc, copper, as well as to copper depletion. Furthermore, we analyzed the transcriptome of a metal-responsive transcription factor (MTF-1) null mutant. The gene family encoding metallothioneins, and the ABC transporter CG10505 that encodes a homolog of ‘yeast cadmium factor’ were induced by all three metals. Zinc and cadmium responses have similar features: genes upregulated by both metals include those for glutathione S-transferases GstD2 and GstD5, and for zinc transporter-like proteins designated ZnT35C and ZnT63C. Several of the metal-induced genes that emerged in our study are regulated by the transcription factor MTF-1. mRNA studies in MTF-1 overexpressing or null mutant flies and in silico search for metal response elements (binding sites for MTF-1) confirmed novel MTF-1 regulated genes such as ferritins, the ABC transporter CG10505 and the zinc transporter ZnT35C. The latter was analyzed in most detail; biochemical and genetic approaches, including targeted mutation, indicate that ZnT35C is involved in cellular and organismal zinc efflux and plays a major role in zinc detoxification. Oxford University Press 2006-10 2006-09-14 /pmc/articles/PMC1635269/ /pubmed/16973896 http://dx.doi.org/10.1093/nar/gkl606 Text en © 2006 The Author(s)
spellingShingle Genomics
Yepiskoposyan, Hasmik
Egli, Dieter
Fergestad, Tim
Selvaraj, Anand
Treiber, Carina
Multhaup, Gerd
Georgiev, Oleg
Schaffner, Walter
Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title_full Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title_fullStr Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title_full_unstemmed Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title_short Transcriptome response to heavy metal stress in Drosophila reveals a new zinc transporter that confers resistance to zinc
title_sort transcriptome response to heavy metal stress in drosophila reveals a new zinc transporter that confers resistance to zinc
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635269/
https://www.ncbi.nlm.nih.gov/pubmed/16973896
http://dx.doi.org/10.1093/nar/gkl606
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