MEK Partner 1 (MP1): Regulation of oligomerization in MAP kinase signaling

Item Type:	Article
Title:	MEK Partner 1 (MP1): Regulation of oligomerization in MAP kinase signaling
Creators Name:	Sharma, C. and Vomastek, T. and Tarcsafalvi, A. and Catling, A.D. and Schaeffer, H.J. and Eblen, S.T. and Weber, M.J.
Abstract:	Specificity in signal transduction can be achieved through scaffolds, anchors, and adapters that assemble generic signal transduction components in specific combinations and locations. MEK Partner-1 (MP1) was identified as a potential "scaffold" protein for the mammalian extracellular signal-regulated kinase (ERK) pathway. To gain insight into the interactions of MP1 with the ERK pathway, we analyzed the ability of MP1 to bind to MEK1, ERK1, and to itself, and the regulation of these interactions. Gel filtration of cell lysates revealed two major MP1 peaks: a broad high molecular weight peak and a 28 kDa complex. An MP1 mutant that lost MEK1 binding no longer enhanced RasV12-stimulated ERK1 activity, and functioned as a dominant negative, consistent with the concept that MP1 function depends on facilitating these oligomerizations. Activation of the ERK pathway by serum or by RasV12 did not detectably affect MP1-MP1 dimerization or MP1-MEK1 interactions, but caused the dissociation of the MP1-ERK1 complex. Surprisingly, pharmacological inhibition of ERK activation did not restore the complex, suggesting that regulation of complex formation occurs independently of ERK phosphorylation. These results support the concept that MP1 functions as a regulator of MAP kinase signaling by binding to MEK1 and regulating its association with a larger signaling complex that may sequentially service multiple molecules of ERK.
Keywords:	ERK1, MAP kinase, MEK1, MP1, Scaffold, Animals
Source:	Journal of Cellular Biochemistry
ISSN:	0730-2312
Publisher:	Wiley
Volume:	94
Number:	4
Page Range:	708-719
Date:	1 January 2005
Official Publication:	https://doi.org/10.1002/jcb.20344
PubMed:	View item in PubMed

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