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- Publisher Website: 10.1073/pnas.1010721108
- Scopus: eid_2-s2.0-79952582563
- PMID: 21282621
- WOS: WOS:000287377000024
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Article: Thiol peroxidases mediate specific genome-wide regulation of gene expression in response to hydrogen peroxide
Title | Thiol peroxidases mediate specific genome-wide regulation of gene expression in response to hydrogen peroxide | ||||
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Authors | |||||
Issue Date | 2011 | ||||
Publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | ||||
Citation | Proceedings Of The National Academy Of Sciences Of The United States Of America, 2011, v. 108 n. 7, p. 2729-2734 How to Cite? | ||||
Abstract | Hydrogen peroxide is thought to regulate cellular processes by direct oxidation of numerous cellular proteins, whereas antioxidants, most notably thiol peroxidases, are thought to reduce peroxides and inhibit H 2O 2 response. However, thiol peroxidases have also been implicated in activation of transcription factors and signaling. It remains unclear if these enzymes stimulate or inhibit redox regulation and whether this regulation is widespread or limited to a few cellular components. Herein, we found that Saccharomyces cerevisiae cells lacking all eight thiol peroxidases were viable and withstood redox stresses. They transcriptionally responded to various redox treatments, but were unable to activate and repress gene expression in response to H 2O 2. Further studies involving redox transcription factors suggested that thiol peroxidases are major regulators of global gene expression in response to H 2O 2. The data suggest that thiol peroxidases sense and transfer oxidative signals to the signaling proteins and regulate transcription, whereas a direct interaction between H 2O 2 and other cellular proteins plays a secondary role. | ||||
Persistent Identifier | http://hdl.handle.net/10722/147629 | ||||
ISSN | 2023 Impact Factor: 9.4 2023 SCImago Journal Rankings: 3.737 | ||||
ISI Accession Number ID |
Funding Information: We thank S. V. Avery (University of Nottingham, Nottingham, United Kingdom) and G. F. Merrill (Oregon State University, Corvallis, OR) for providing yeast strains, A. Bird for help with microarrays, and the University of Utah Microarray Core Facility for excellent technical assistance. This work was supported by National Institutes of Health (NIH) Grant GM065204 (to V.N.G.). J.C.R. was supported by NIH Grant GM083292 (to D.R.W.). | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Fomenko, DE | en_US |
dc.contributor.author | Koc, A | en_US |
dc.contributor.author | Agisheva, N | en_US |
dc.contributor.author | Jacobsen, M | en_US |
dc.contributor.author | Kaya, A | en_US |
dc.contributor.author | Malinouski, M | en_US |
dc.contributor.author | Rutherford, JC | en_US |
dc.contributor.author | Siu, KL | en_US |
dc.contributor.author | Jin, DY | en_US |
dc.contributor.author | Winge, DR | en_US |
dc.contributor.author | Gladyshev, VN | en_US |
dc.date.accessioned | 2012-05-29T06:05:05Z | - |
dc.date.available | 2012-05-29T06:05:05Z | - |
dc.date.issued | 2011 | en_US |
dc.identifier.citation | Proceedings Of The National Academy Of Sciences Of The United States Of America, 2011, v. 108 n. 7, p. 2729-2734 | en_US |
dc.identifier.issn | 0027-8424 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/147629 | - |
dc.description.abstract | Hydrogen peroxide is thought to regulate cellular processes by direct oxidation of numerous cellular proteins, whereas antioxidants, most notably thiol peroxidases, are thought to reduce peroxides and inhibit H 2O 2 response. However, thiol peroxidases have also been implicated in activation of transcription factors and signaling. It remains unclear if these enzymes stimulate or inhibit redox regulation and whether this regulation is widespread or limited to a few cellular components. Herein, we found that Saccharomyces cerevisiae cells lacking all eight thiol peroxidases were viable and withstood redox stresses. They transcriptionally responded to various redox treatments, but were unable to activate and repress gene expression in response to H 2O 2. Further studies involving redox transcription factors suggested that thiol peroxidases are major regulators of global gene expression in response to H 2O 2. The data suggest that thiol peroxidases sense and transfer oxidative signals to the signaling proteins and regulate transcription, whereas a direct interaction between H 2O 2 and other cellular proteins plays a secondary role. | en_US |
dc.language | eng | en_US |
dc.publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | en_US |
dc.relation.ispartof | Proceedings of the National Academy of Sciences of the United States of America | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Gene Expression Regulation - Drug Effects | en_US |
dc.subject.mesh | Hydrogen Peroxide - Toxicity | en_US |
dc.subject.mesh | Models, Biological | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Mutagenesis | en_US |
dc.subject.mesh | Oligonucleotide Array Sequence Analysis | en_US |
dc.subject.mesh | Oxidative Stress - Genetics | en_US |
dc.subject.mesh | Peroxidases - Deficiency - Metabolism | en_US |
dc.subject.mesh | Phenotype | en_US |
dc.subject.mesh | Ribosomal Proteins - Metabolism | en_US |
dc.subject.mesh | Saccharomyces Cerevisiae - Drug Effects - Enzymology - Genetics | en_US |
dc.subject.mesh | Saccharomyces Cerevisiae Proteins - Metabolism | en_US |
dc.subject.mesh | Sequence Analysis, Dna | en_US |
dc.subject.mesh | Signal Transduction - Drug Effects - Physiology | en_US |
dc.title | Thiol peroxidases mediate specific genome-wide regulation of gene expression in response to hydrogen peroxide | en_US |
dc.type | Article | en_US |
dc.identifier.email | Jin, DY:dyjin@hkucc.hku.hk | en_US |
dc.identifier.authority | Jin, DY=rp00452 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1073/pnas.1010721108 | en_US |
dc.identifier.pmid | 21282621 | - |
dc.identifier.scopus | eid_2-s2.0-79952582563 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79952582563&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 108 | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.spage | 2729 | en_US |
dc.identifier.epage | 2734 | en_US |
dc.identifier.isi | WOS:000287377000024 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Fomenko, DE=6602197028 | en_US |
dc.identifier.scopusauthorid | Koc, A=7006124626 | en_US |
dc.identifier.scopusauthorid | Agisheva, N=36672465400 | en_US |
dc.identifier.scopusauthorid | Jacobsen, M=42761582100 | en_US |
dc.identifier.scopusauthorid | Kaya, A=26424286000 | en_US |
dc.identifier.scopusauthorid | Malinouski, M=22835482500 | en_US |
dc.identifier.scopusauthorid | Rutherford, JC=7101706816 | en_US |
dc.identifier.scopusauthorid | Siu, KL=35327996300 | en_US |
dc.identifier.scopusauthorid | Jin, DY=7201973614 | en_US |
dc.identifier.scopusauthorid | Winge, DR=7006036381 | en_US |
dc.identifier.scopusauthorid | Gladyshev, VN=35236886300 | en_US |
dc.identifier.issnl | 0027-8424 | - |