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Molecular and Cellular Biology, July 2008, p. 4562-4575, Vol. 28, No. 14
0270-7306/08/$08.00+0     doi:10.1128/MCB.00165-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

MKP-1 mRNA Stabilization and Translational Control by RNA-Binding Proteins HuR and NF90{triangledown} ,{dagger}

Yuki Kuwano, Hyeon Ho Kim, Kotb Abdelmohsen, Rudolf Pullmann Jr., Jennifer L. Martindale, Xiaoling Yang, and Myriam Gorospe*

Laboratory of Cellular and Molecular Biology, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21228

Received 1 February 2008/ Returned for modification 5 March 2008/ Accepted 7 May 2008

The mitogen-activated protein (MAP) kinase phosphatase 1 (MKP-1) plays a major role in dephosphorylating and thereby inactivating the MAP kinases extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38. Here, we examine the posttranscriptional events underlying the robust MKP-1 induction by oxidants in HeLa cells. H2O2 treatment potently stabilized the MKP-1 mRNA and increased the association of MKP-1 mRNA with the translation machinery. Four RNA-binding proteins (RNA-BPs) that influence mRNA turnover and/or translation (HuR, NF90, TIAR, and TIA-1) were found to bind to biotinylated transcripts spanning the MKP-1 AU-rich 3' untranslated region. By using ribonucleoprotein immunoprecipitation analysis, we showed that H2O2 treatment increased the association of MKP-1 mRNA with HuR and NF90 and decreased its association with the translational repressors TIAR and TIA-1. HuR or NF90 silencing significantly diminished the H2O2-stimulated MKP-1 mRNA stability; HuR silencing also markedly decreased MKP-1 translation. In turn, lowering MKP-1 expression in HuR-silenced cultures resulted in substantially elevated phosphorylation of JNK and p38 after H2O2 treatment. Collectively, MKP-1 upregulation by oxidative stress is potently influenced by increased mRNA stability and translation, mediated at least in part by the RNA-BPs HuR and NF90.


* Corresponding author. Mailing address: Box 12, LCMB, NIA-IRP, NIH, 5600 Nathan Shock Dr., Baltimore, MD 21224. Phone: (410) 558-8443. Fax: (410) 558-8386. E-mail: myriam-gorospe{at}nih.gov

{triangledown} Published ahead of print on 19 May 2008.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.


Molecular and Cellular Biology, July 2008, p. 4562-4575, Vol. 28, No. 14
0270-7306/08/$08.00+0     doi:10.1128/MCB.00165-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




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