ID | 116315 |
Title Alternative | KLHDC10 Activates ASK1 by Suppressing PP5
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Author |
Sekine, Yusuke
The University of Tokyo
Hatanaka, Ryo
The University of Tokyo
Watanabe, Takeshi
The University of Tokyo
Tokushima University Educator and Researcher Directory
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Sono, Naoki
The University of Tokyo
Iemura, Shun-ichiro
National Institutes of Advanced Industrial Science and Technology|Fukushima Medical University
Natsume, Tohru
National Institutes of Advanced Industrial Science and Technology
Kuranaga, Erina
The University of Tokyo|RIKEN
Miura, Masayuki
The University of Tokyo
Takeda, Kohsuke
The University of Tokyo|Nagasaki University
Ichijo, Hidenori
The University of Tokyo
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Content Type |
Journal Article
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Description | Reactive oxygen species (ROS)-induced activation of Apoptosis signal-regulating kinase 1 (ASK1) plays crucial roles in oxidative stress-mediated cell death through the activation of the JNK and p38 MAPK pathways. However, the regulatory mechanism of ASK1 in the oxidative stress response remains to be elucidated. Here, we identified the kelch repeat protein, Slim, as an activator of ASK1 through a Drosophila misexpression screen. We also performed a proteomics screen and revealed that Kelch domain containing 10 (KLHDC10), a mammalian ortholog of Slim, interacted with Protein phosphatase 5 (PP5), which has been shown to inactivate ASK1 in response to ROS. KLHDC10 bound to the phosphatase domain of PP5 and suppressed its phosphatase activity. Moreover, KLHDC10 was required for H2O2-induced sustained activation of ASK1 and cell death in Neuro2A cells. These findings suggest that Slim/KLHDC10 is an activator of ASK1, contributing to oxidative stress-induced cell death through the suppression of PP5.
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Journal Title |
Molecular Cell
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ISSN | 10974164
10972765
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NCID | AA12191342
AA1119005X
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Publisher | Elsevier|Cell Press
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Volume | 48
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Issue | 5
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Start Page | 692
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End Page | 704
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Published Date | 2012-10-25
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Rights | Open Archive
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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
Publisher
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departments |
Medical Sciences
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