Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 285, Issue 40, Pages 30959-30970Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M110.138370
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Funding
- National Research Foundation of Korea [R0A-2007-000-20006-0]
- Chungbuk National University
- National Research Foundation of Korea [2007-0056620] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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The present study demonstrated that murine protein serine/threonine kinase 38 (MPK38) coimmunoprecipitates with Smad proteins (Smad2, -3, -4, and -7) and that this association is mediated by the catalytic kinase domain of MPK38. The association between MPK38 and Smad2, -3, and -4 was significantly increased by TGF-beta or ASK1 signals, whereas these signals decreased association of MPK38 with Smad7. MPK38 stimulated TGF-beta-induced transcription required for TGF-beta-mediated biological functions, such as apoptosis and cell growth arrest, in a kinase-dependent manner. Knockdown of endogenous MPK38 showed an opposite effect, inhibiting TGF-beta signaling. MPK38-mediated phosphorylation of Smad proteins (Ser(245) of Smad2, Ser(204) of Smad3, Ser(343) of Smad4, and Thr(96) of Smad7) was also found to be crucial to the positive regulation of TGF-beta signaling induced by MPK38. In addition, MPK38 enhanced nuclear translocation of Smad3, as well as redistribution of Smad7 from the nucleus to the cytoplasm, in response to TGF-beta. Together, these results indicate that MPK38 functions as a stimulator of TGF-beta signaling through direct interaction with and phosphorylation of Smad proteins.
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