Retinoblastoma-binding Protein 4-regulated Classical Nuclear Transport Is Involved in Cellular Senescence
- J Biol Chem. 2015 Dec 4;290(49):29375-88. doi: 10.1074/jbc.M115.681908.
- 1. From the Graduate School of Medicine and the Laboratories of Nuclear Transport Dynamics and.
- 2. the Laboratories of Nuclear Transport Dynamics and.
- 3. Bioinformatics.
- 4. the Graduate School of Life Science, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan.
- 5. the Laboratories of Nuclear Transport Dynamics and Laboratory of Biomedical Innovation, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, [email protected].
- 6. Laboratory of Biomedical Innovation, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, National Institutes of Biomedical Innovation, Health and Nutrition, Ibaraki, Osaka 567-0085, and [email protected].
Nucleocytoplasmic trafficking is a fundamental cellular process in eukaryotic cells. Here, we demonstrated that retinoblastoma-binding protein 4 (RBBP4) functions as a novel regulatory factor to increase the efficiency of importin α/β-mediated nuclear import. RBBP4 accelerates the release of importin β1 from importin α via competitive binding to the importin β-binding domain of importin α in the presence of RanGTP. Therefore, it facilitates importin α/β-mediated nuclear import. We showed that the importin α/β pathway is down-regulated in replicative senescent cells, concomitant with a decrease in RBBP4 level. Knockdown of RBBP4 caused both suppression of nuclear transport and induction of cellular senescence. This is the first report to identify a factor that competes with importin β1 to bind to importin α, and it demonstrates that the loss of this factor can trigger cellular senescence.
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target: Biochemical Assay ReagentsResearch Areas: Others
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target: Biochemical Assay ReagentsResearch Areas: Others