IMR Press / FBL / Volume 11 / Issue 3 / DOI: 10.2741/2001

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article

Dual Specificity Phosphotase 18, Interacting with SAPK, Dephosphorylates SAPK and Inhibits SAPK/JNK Signal Pathway in vivo

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1 State Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Science, Fudan University, Shanghai 200433, People's Republic of China
2 Department of Cardiothoracic Surgery, Changhai Hospital, Second Military Medical University, Shanghai, People’s Republic of China
Front. Biosci. (Landmark Ed) 2006, 11(3), 2714–2724; https://doi.org/10.2741/2001
Published: 1 September 2006
Abstract

The SAPK/JNKs play important roles in numerous cellular processes, and for this reason they have become putative drug targets. Most dual-specificity protein phosphatases (DSPs) play important roles in the regulation of mitogenic signal transduction and cell cycle control in response to extracellular stimuli. Dual-specificity phosphatase 18 (DUSP18), a newly recognized SAPK/JNK phosphatase, is widely expressed. This expression is modulated in response to extracellular stimuli. By phosphorylation assay, pull down and coimmunoprecipitation experiments, it is shown here that DUSP18 interacts with SAPK/JNK and dephosphorylates it both in vitro and in vivo. DUSP18 does not dephosphorylate p38 or p44ERK1. Furthermore, DUSP18 inhibits SAPK/JNK pathway in vivo. Based on these findings, DUSP18 appears to serve an important role by regulation of SAPK/JNK pathway.

Keywords
Kinase
DUSP18
SAPK
JNK
Phosphorylation
Interaction
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