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RASSF2 Is a Novel K-Ras-specific Effector and Potential Tumor Suppressor
- Source :
- Journal of Biological Chemistry. 278:28045-28051
- Publication Year :
- 2003
- Publisher :
- Elsevier BV, 2003.
-
Abstract
- Ras proteins regulate a wide range of biological processes by interacting with a broad assortment of effector proteins. Although activated forms of Ras are frequently associated with oncogenesis, they may also provoke growth-antagonistic effects. These include senescence, cell cycle arrest, differentiation, and apoptosis. The mechanisms that underlie these growth-inhibitory activities are relatively poorly understood. Recently, two related novel Ras effectors, NORE1 and RASSF1, have been identified as mediators of apoptosis and cell cycle arrest. Both of these proteins exhibit many of the properties normally associated with tumor suppressors. We now identify a novel third member of this family, designated RASSF2. RASSF2 binds directly to K-Ras in a GTP-dependent manner via the Ras effector domain. However, RASSF2 only weakly interacts with H-Ras. Moreover, RASSF2 promotes apoptosis and cell cycle arrest and is frequently down-regulated in lung tumor cell lines. Thus, we identify RASSF2 as a new member of the RASSF1 family of Ras effectors/tumor suppressors that exhibits a specificity for interacting with K-Ras.
- Subjects :
- Programmed cell death
Cell cycle checkpoint
Cell division
Cellular differentiation
Blotting, Western
Down-Regulation
Apoptosis
Cell Separation
Plasma protein binding
Biology
Transfection
medicine.disease_cause
Biochemistry
Cell Line
Anti-apoptotic Ras signalling cascade
Tumor Cells, Cultured
medicine
Animals
Humans
Genes, Tumor Suppressor
Tissue Distribution
Amino Acid Sequence
Molecular Biology
Cellular Senescence
Glutathione Transferase
Cell Death
Sequence Homology, Amino Acid
Effector
Tumor Suppressor Proteins
Proteins
Cell Differentiation
DNA
Cell Biology
Flow Cytometry
Recombinant Proteins
Protein Structure, Tertiary
Cell biology
COS Cells
ras Proteins
Guanosine Triphosphate
Carcinogenesis
Cell Division
Plasmids
Protein Binding
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 278
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....a585978594938f4769a5a440ed413ea5