GlutaredoxinV1, Main, Exploration, bibRecord, 000923

Redox regulation of the tumor suppressor PTEN by glutaredoxin 5 and Ycp4.

Identifieur interne : 000923 ( Main/Exploration ); précédent : 000922; suivant : 000924

Redox regulation of the tumor suppressor PTEN by glutaredoxin 5 and Ycp4.

Auteurs : Yujeong Kim [Corée du Sud] ; Kee-Oh Chay ; Inyoung Kim ; Yong Bhum Song ; Tae-Youl Kim ; Seong-Jeong Han ; Younghee Ahn ; Seung-Hyun Cho ; Kwang-Lae Hoe ; Bong Whan Ahn ; Won-Ki Huh ; Seung-Rock Lee

Source :

Biochemical and biophysical research communications [ 1090-2104 ] ; 2011.

RBID : pubmed:21371429

Descripteurs français

English descriptors

KwdEn :
- Amino Acid Sequence (MeSH), Flavodoxin (metabolism), Glutaredoxins (genetics), Glutaredoxins (metabolism), Humans (MeSH), Hydrogen Peroxide (metabolism), Molecular Sequence Data (MeSH), Oxidation-Reduction (MeSH), PTEN Phosphohydrolase (genetics), PTEN Phosphohydrolase (metabolism), Saccharomyces cerevisiae (genetics), Saccharomyces cerevisiae (metabolism), Saccharomyces cerevisiae Proteins (metabolism).
MESH :
- chemical , genetics : Glutaredoxins, PTEN Phosphohydrolase.
- chemical , metabolism : Flavodoxin, Glutaredoxins, Hydrogen Peroxide, PTEN Phosphohydrolase, Saccharomyces cerevisiae Proteins.
- genetics : Saccharomyces cerevisiae.
- metabolism : Saccharomyces cerevisiae.
- Amino Acid Sequence, Humans, Molecular Sequence Data, Oxidation-Reduction.

Abstract

Human PTEN (phosphatase and tensin homolog deleted on chromosome 10; a phosphatidylinositol 3-phosphatase) expressed in Saccharomyces cerevisiae was oxidized in a time- and H(2)O(2)-concentration-dependent manner. Oxidized hPTEN was reduced by cellular reductants as in human cells. The reduction rate of oxidized hPTEN was monitored in S. cerevisiae mutants in which the genes involved in redox homeostasis had been disrupted. Reduction of hPTEN was delayed in each of S. cerevisiae grx5Δ and ycp4Δ mutants. Expression of Grx5 and Ycp4 in each of the mutants rescued the reduction rate of oxidized hPTEN. Furthermore, an in vitro assay revealed that the human Grx5/GSH system efficiently catalyzed the reduction of oxidized hPTEN. These results suggest that the reduction of oxidized hPTEN is regulated by Grx5 and Ycp4.

DOI: 10.1016/j.bbrc.2011.02.133
PubMed: 21371429

Affiliations:

Corée du Sud

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 000939
to stream Main, to step Curation: 000939

Le document en format XML

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<author><name sortKey="Chay, Kee Oh" sort="Chay, Kee Oh" uniqKey="Chay K" first="Kee-Oh" last="Chay">Kee-Oh Chay</name>
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<author><name sortKey="Kim, Inyoung" sort="Kim, Inyoung" uniqKey="Kim I" first="Inyoung" last="Kim">Inyoung Kim</name>
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<author><name sortKey="Song, Yong Bhum" sort="Song, Yong Bhum" uniqKey="Song Y" first="Yong Bhum" last="Song">Yong Bhum Song</name>
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<author><name sortKey="Kim, Tae Youl" sort="Kim, Tae Youl" uniqKey="Kim T" first="Tae-Youl" last="Kim">Tae-Youl Kim</name>
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<author><name sortKey="Han, Seong Jeong" sort="Han, Seong Jeong" uniqKey="Han S" first="Seong-Jeong" last="Han">Seong-Jeong Han</name>
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<author><name sortKey="Cho, Seung Hyun" sort="Cho, Seung Hyun" uniqKey="Cho S" first="Seung-Hyun" last="Cho">Seung-Hyun Cho</name>
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<series><title level="j">Biochemical and biophysical research communications</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence (MeSH)</term>
<term>Flavodoxin (metabolism)</term>
<term>Glutaredoxins (genetics)</term>
<term>Glutaredoxins (metabolism)</term>
<term>Humans (MeSH)</term>
<term>Hydrogen Peroxide (metabolism)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>PTEN Phosphohydrolase (genetics)</term>
<term>PTEN Phosphohydrolase (metabolism)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Saccharomyces cerevisiae Proteins (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Données de séquences moléculaires (MeSH)</term>
<term>Flavodoxine (métabolisme)</term>
<term>Glutarédoxines (génétique)</term>
<term>Glutarédoxines (métabolisme)</term>
<term>Humains (MeSH)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Peroxyde d'hydrogène (métabolisme)</term>
<term>Phosphohydrolase PTEN (génétique)</term>
<term>Phosphohydrolase PTEN (métabolisme)</term>
<term>Protéines de Saccharomyces cerevisiae (métabolisme)</term>
<term>Saccharomyces cerevisiae (génétique)</term>
<term>Saccharomyces cerevisiae (métabolisme)</term>
<term>Séquence d'acides aminés (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Glutaredoxins</term>
<term>PTEN Phosphohydrolase</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Flavodoxin</term>
<term>Glutaredoxins</term>
<term>Hydrogen Peroxide</term>
<term>PTEN Phosphohydrolase</term>
<term>Saccharomyces cerevisiae Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Glutarédoxines</term>
<term>Phosphohydrolase PTEN</term>
<term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Flavodoxine</term>
<term>Glutarédoxines</term>
<term>Peroxyde d'hydrogène</term>
<term>Phosphohydrolase PTEN</term>
<term>Protéines de Saccharomyces cerevisiae</term>
<term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Oxidation-Reduction</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Oxydoréduction</term>
<term>Séquence d'acides aminés</term>
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<front><div type="abstract" xml:lang="en">Human PTEN (phosphatase and tensin homolog deleted on chromosome 10; a phosphatidylinositol 3-phosphatase) expressed in Saccharomyces cerevisiae was oxidized in a time- and H(2)O(2)-concentration-dependent manner. Oxidized hPTEN was reduced by cellular reductants as in human cells. The reduction rate of oxidized hPTEN was monitored in S. cerevisiae mutants in which the genes involved in redox homeostasis had been disrupted. Reduction of hPTEN was delayed in each of S. cerevisiae grx5Δ and ycp4Δ mutants. Expression of Grx5 and Ycp4 in each of the mutants rescued the reduction rate of oxidized hPTEN. Furthermore, an in vitro assay revealed that the human Grx5/GSH system efficiently catalyzed the reduction of oxidized hPTEN. These results suggest that the reduction of oxidized hPTEN is regulated by Grx5 and Ycp4.</div>
</front>
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<ArticleTitle>Redox regulation of the tumor suppressor PTEN by glutaredoxin 5 and Ycp4.</ArticleTitle>
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<Abstract><AbstractText>Human PTEN (phosphatase and tensin homolog deleted on chromosome 10; a phosphatidylinositol 3-phosphatase) expressed in Saccharomyces cerevisiae was oxidized in a time- and H(2)O(2)-concentration-dependent manner. Oxidized hPTEN was reduced by cellular reductants as in human cells. The reduction rate of oxidized hPTEN was monitored in S. cerevisiae mutants in which the genes involved in redox homeostasis had been disrupted. Reduction of hPTEN was delayed in each of S. cerevisiae grx5Δ and ycp4Δ mutants. Expression of Grx5 and Ycp4 in each of the mutants rescued the reduction rate of oxidized hPTEN. Furthermore, an in vitro assay revealed that the human Grx5/GSH system efficiently catalyzed the reduction of oxidized hPTEN. These results suggest that the reduction of oxidized hPTEN is regulated by Grx5 and Ycp4.</AbstractText>
<CopyrightInformation>Copyright © 2011 Elsevier Inc. All rights reserved.</CopyrightInformation>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kim</LastName>
<ForeName>Yujeong</ForeName>
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<Author ValidYN="Y"><LastName>Huh</LastName>
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<Author ValidYN="Y"><LastName>Lee</LastName>
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<Chemical><RegistryNumber>0</RegistryNumber>
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<Chemical><RegistryNumber>0</RegistryNumber>
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<Chemical><RegistryNumber>BBX060AN9V</RegistryNumber>
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<Chemical><RegistryNumber>EC 3.1.3.67</RegistryNumber>
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<Chemical><RegistryNumber>EC 3.1.3.67</RegistryNumber>
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<name sortKey="Han, Seong Jeong" sort="Han, Seong Jeong" uniqKey="Han S" first="Seong-Jeong" last="Han">Seong-Jeong Han</name>
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<name sortKey="Kim, Inyoung" sort="Kim, Inyoung" uniqKey="Kim I" first="Inyoung" last="Kim">Inyoung Kim</name>
<name sortKey="Kim, Tae Youl" sort="Kim, Tae Youl" uniqKey="Kim T" first="Tae-Youl" last="Kim">Tae-Youl Kim</name>
<name sortKey="Lee, Seung Rock" sort="Lee, Seung Rock" uniqKey="Lee S" first="Seung-Rock" last="Lee">Seung-Rock Lee</name>
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	Serveur d'exploration sur la glutarédoxine
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Serveur d'exploration sur la glutarédoxine

Redox regulation of the tumor suppressor PTEN by glutaredoxin 5 and Ycp4.

Redox regulation of the tumor suppressor PTEN by glutaredoxin 5 and Ycp4.

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