Activation of MK5/PRAK by the atypical MAP kinase ERK3 defines a novel signal transduction pathway |
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Authors: | Seternes Ole-Morten Mikalsen Theresa Johansen Bjarne Michaelsen Espen Armstrong Chris G Morrice Nick A Turgeon Benjamin Meloche Sylvain Moens Ugo Keyse Stephen M |
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Affiliation: | Department of Pharmacology, Institute of Medical Biology, University of Troms?, Troms?, Norway. olems@fagmed.uit.no |
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Abstract: | Extracellular signal-regulated kinase 3 (ERK3) is an atypical mitogen-activated protein kinase (MAPK), which is regulated by protein stability. However, its function is unknown and no physiological substrates for ERK3 have yet been identified. Here we demonstrate a specific interaction between ERK3 and MAPK-activated protein kinase-5 (MK5). Binding results in nuclear exclusion of both ERK3 and MK5 and is accompanied by ERK3-dependent phosphorylation and activation of MK5 in vitro and in vivo. Endogenous MK5 activity is significantly reduced by siRNA-mediated knockdown of ERK3 and also in fibroblasts derived from ERK3-/- mice. Furthermore, increased levels of ERK3 protein detected during nerve growth factor-induced differentiation of PC12 cells are accompanied by an increase in MK5 activity. Conversely, MK5 depletion causes a dramatic reduction in endogenous ERK3 levels. Our data identify the first physiological protein substrate for ERK3 and suggest a functional link between these kinases in which MK5 is a downstream target of ERK3, while MK5 acts as a chaperone for ERK3. Our findings provide valuable tools to further dissect the regulation and biological roles of both ERK3 and MK5. |
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Keywords: | differentiation ERK3 MK5 phosphorylation signalling |
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