Reference : Context-specific flow through the MEK/ERK module produces cell- and ligand-specific p...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/10993/24176
Context-specific flow through the MEK/ERK module produces cell- and ligand-specific patterns of ERK single and double phosphorylation.
English
Iwamoto, Nao [> >]
D'Alessandro, Lorenza A. [> >]
Depner, Sofia [> >]
Hahn, Bettina [> >]
Kramer, Bernhard A. [> >]
Lucarelli, Philippe mailto [University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
Vlasov, Artyom [> >]
Stepath, Markus [> >]
Bohm, Martin E. [> >]
Deharde, Daniela [> >]
Damm, Georg [> >]
Seehofer, Daniel [> >]
Lehmann, Wolf D. [> >]
Klingmuller, Ursula [> >]
Schilling, Marcel [> >]
2016
Science signaling
9
413
ra13
Yes (verified by ORBilu)
International
1937-9145
United States
[en] The same pathway, such as the mitogen-activated protein kinase (MAPK) pathway, can produce different cellular responses, depending on stimulus or cell type. We examined the phosphorylation dynamics of the MAPK kinase MEK and its targets extracellular signal-regulated kinase 1 and 2 (ERK1/2) in primary hepatocytes and the transformed keratinocyte cell line HaCaT A5 exposed to either hepatocyte growth factor or interleukin-6. By combining quantitative mass spectrometry with dynamic modeling, we elucidated network structures for the reversible threonine and tyrosine phosphorylation of ERK in both cell types. In addition to differences in the phosphorylation and dephosphorylation reactions, the HaCaT network model required two feedback mechanisms, which, as the experimental data suggested, involved the induction of the dual-specificity phosphatase DUSP6 and the scaffold paxillin. We assayed and modeled the accumulation of the double-phosphorylated and active form of ERK1/2, as well as the dynamics of the changes in the monophosphorylated forms of ERK1/2. Modeling the differences in the dynamics of the changes in the distributions of the phosphorylated forms of ERK1/2 suggested that different amounts of MEK activity triggered context-specific responses, with primary hepatocytes favoring the formation of double-phosphorylated ERK1/2 and HaCaT A5 cells that produce both the threonine-phosphorylated and the double-phosphorylated form. These differences in phosphorylation distributions explained the threshold, sensitivity, and saturation of the ERK response. We extended the findings of differential ERK phosphorylation profiles to five additional cultured cell systems and matched liver tumor and normal tissue, which revealed context-specific patterns of the various forms of phosphorylated ERK.
http://hdl.handle.net/10993/24176
10.1126/scisignal.aab1967
Copyright (c) 2016, American Association for the Advancement of Science.

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