HDAC3 is linked to cell cycle machinery in MiaPaCa2 cells by regulating transcription of skp2

G. Schneider, M. Reichert, D. Saur, R. Hamacher, R. Fritsch, R. M. Schmid

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

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 languageEnglish
Pages (from-to)522-531
Number of pages10
JournalCell Proliferation
Volume40
Issue number4
DOIs
StatePublished - Aug 2007

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