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PMID: 15381250 Published · ppublish English Journal Article Review

Counting on mitogen-activated protein kinases--ERKs 3, 4, 5, 6, 7 and 8.

Cellular signalling ·Vol. 16 ·No. 12 ·2004-12-00 ·Pages 1345-54

Bogoyevitch MA, Court NW

Abstract

Signal transduction pathways in eukaryotic cells integrate diverse extracellular signals, and regulate complex biological responses such as growth, differentiation and death. One group of proline-directed Ser/Thr protein kinases, the mitogen-activated protein kinases (MAPKs), plays a central role in these signalling pathways. Much attention has focused in recent years on three subfamilies of MAPKs, the extracellular signal regulated kinases (ERKs), c-Jun N-terminal kinases (JNKs) and the p38 MAPKs. However, the ERK family is broader than the ERK1 and ERK2 proteins that have been the subject of most studies in this area. Here we overview the work on ERKs 3 to 8, emphasising where possible their biological activities as well as distinctive biochemical properties. It is clear from these studies that these additional ERKs show similarities to ERK1 and ERK2, but with some interesting differences that challenge the paradigm of the archetypical ERK1/2 MAPK pathway.

MeSH Terms
Animals Extracellular Signal-Regulated MAP Kinases/physiology Humans MAP Kinase Signaling System Mice Mitogen-Activated Protein Kinase 12/physiology Mitogen-Activated Protein Kinase 6/physiology Mitogen-Activated Protein Kinase 7/physiology Phosphorylation Signal Transduction
Chemicals
Mitogen-Activated Protein Kinase 12 Extracellular Signal-Regulated MAP Kinases MAPK15 protein, human Mapk15 protein, rat Mitogen-Activated Protein Kinase 6 Mitogen-Activated Protein Kinase 7
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bogoyevitch Marie A
Cell Signalling Laboratory, Biochemistry and Molecular Biology, School of Biomedical and Chemical Sciences, University of Western Australia, Crawley, WA 6009, Australia. marieb@cyllene.uwa.edu.au
Court Naomi W
Article Info
Journal
Cellular signalling
Abbr.
Cell Signal
ISSN
0898-6568
Published
2004-12-00
Pages
1345-54
Language
English
Region
England
NLM ID
8904683
Subset
IM
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