Home LiteratureArticle Details
PMID: 17052209 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

The role of scaffold proteins in MEK/ERK signalling.

Biochemical Society transactions ·Vol. 34 ·No. Pt 5 ·2006-11-00 ·Pages 833-6

Sacks DB

Abstract

Signal transduction networks allow cells to recognize and respond to changes in the extracellular environment. All eukaryotic cells have MAPK (mitogen-activated protein kinase) pathways that participate in diverse cellular functions, including differentiation, survival, transformation and movement. Five distinct groups of MAPKs have been characterized in mammals, the most extensively studied of which is the Ras/Raf/MEK [MAPK/ERK (extracellular-signal-regulated kinase) kinase]/ERK cascade. Numerous stimuli, including growth factors and phorbol esters, activate MEK/ERK signalling. How disparate extracellular signals are translated by MEK/ERK into different cellular functions remains obscure. Originally identified in yeast, scaffold proteins are now recognized to contribute to the specificity of MEK/ERK pathways in mammalian cells. These scaffolds include KSR (kinase suppressor of Ras), beta-arrestin, MEK partner-1, Sef and IQGAP1. Scaffolds organize multiprotein signalling complexes. This targets MEK/ERK to specific substrates and facilitates communication with other pathways, thereby mediating diverse functions. The adaptor proteins regulate the kinetics, amplitude and localization of MEK/ERK signalling, providing an efficient mechanism that enables an individual extracellular stimulus to promote a specific biological response.

MeSH Terms
Animals Kinetics MAP Kinase Kinase Kinases/metabolism Mitogen-Activated Protein Kinases/metabolism Models, Biological Nuclear Matrix-Associated Proteins/physiology Signal Transduction/physiology Substrate Specificity
Chemicals
Nuclear Matrix-Associated Proteins Mitogen-Activated Protein Kinases MAP Kinase Kinase Kinases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Sacks D B
Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Thorn 530, 75 Francis Street, Boston, MA 02115, USA. [email protected]
Article Info
Journal
Biochemical Society transactions
Abbr.
Biochem Soc Trans
ISSN
0300-5127
Published
2006-11-00
Pages
833-6
Language
English
Region
England
NLM ID
7506897
Subset
IM
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