Abstract
Objective: Histone deacetylases (HDACs) have been linked to cell cycle control in various models, involving regulation of the cyclin-dependent kinase inhibitor p27Kip1. Results: Here, we demonstrate that HDAC inhibition by trichostatin A reduces S-phase kinase-associated protein 2 mRNA and protein abundance. Furthermore, in contrast to HDAC1, recruited to the skp2 promoter in the G0 phase, HDAC3 is bound in early S phase. Activating function of HDAC3 towards the skp2 gene has been validated using RNA interference techniques. siRNAs, targeting HDAC3 specifically, reduced skp2 transcription. Conclusion: These findings propose that the skp2 gene is a novel target of HDAC3, mediating cell cycle control and oncogenesis.
| Original language | English |
|---|---|
| Pages (from-to) | 522-531 |
| Number of pages | 10 |
| Journal | Cell Proliferation |
| Volume | 40 |
| Issue number | 4 |
| DOIs | |
| State | Published - Aug 2007 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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