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Regulation and function of the RSK family of protein kinases
- Source :
- Biochemical Journal. 441:553-569
- Publication Year :
- 2011
- Publisher :
- Portland Press Ltd., 2011.
-
Abstract
- The RSK (90 kDa ribosomal S6 kinase) family comprises a group of highly related serine/threonine kinases that regulate diverse cellular processes, including cell growth, proliferation, survival and motility. This family includes four vertebrate isoforms (RSK1, RSK2, RSK3 and RSK4), and single family member orthologues are also present in Drosophila and Caenorhabditis elegans. The RSK isoforms are downstream effectors of the Ras/ERK (extracellular-signal-regulated kinase) signalling pathway. Significant advances in the field of RSK signalling have occurred in the past few years, including several new functions ascribed to the RSK isoforms, the discovery of novel protein substrates and the implication of different RSK isoforms in cancer. Collectively, these new findings increase the diversity of biological functions regulated by RSK, and highlight potential new directions of research. In the present paper, we review the structure, expression and activation mechanisms of the RSK isoforms, and discuss their physiological roles on the basis of established substrates and recent discoveries.
- Subjects :
- MAPK/ERK pathway
Gene isoform
Cell Survival
MAP Kinase Signaling System
Molecular Sequence Data
Ribosomal Protein S6 Kinases, 90-kDa
Biochemistry
Gene Expression Regulation, Enzymologic
Ribosomal s6 kinase
Mice
Cell Movement
Animals
Humans
Amino Acid Sequence
Phosphorylation
Extracellular Signal-Regulated MAP Kinases
Molecular Biology
Caenorhabditis elegans
Cell Proliferation
Regulation of gene expression
biology
Kinase
Effector
Cell Cycle Checkpoints
Cell Biology
biology.organism_classification
Protein Structure, Tertiary
Cell biology
Enzyme Activation
Isoenzymes
biology.protein
Mitogen-Activated Protein Kinases
Sequence Alignment
Subjects
Details
- ISSN :
- 14708728 and 02646021
- Volume :
- 441
- Database :
- OpenAIRE
- Journal :
- Biochemical Journal
- Accession number :
- edsair.doi.dedup.....84d968e24cb6ae017ae1817fcdbdc8be
- Full Text :
- https://doi.org/10.1042/bj20110289