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Volume 243, Issue 1-2 p. 527-536
Free Access

Biochemical and Cellular Effects of Roscovitine, a Potent and Selective Inhibitor of the Cyclin-Dependent Kinases cdc2, cdk2 and cdk5

Laurent Meijer

Corresponding Author

Laurent Meijer

CNRS, Station Biologique, BP 74, Roscoff, France

L. Meijer, CNRS, Station Biologique, BP 74, F-29682 Roscoff cedex. France
Fax:+33 2 98 29 23 42.
E-mail: [email protected]Search for more papers by this author
Annie Borgne

Annie Borgne

CNRS, Station Biologique, BP 74, Roscoff, France

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Odile Mulner

Odile Mulner

CNRS, Station Biologique, BP 74, Roscoff, France

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James P. J. Chong

James P. J. Chong

Imperial Cancer Research Fund, Clare Hall Laboratories, Potter's Bar, UK

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J. Julian Blow

J. Julian Blow

Imperial Cancer Research Fund, Clare Hall Laboratories, Potter's Bar, UK

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Naoyuki Inagaki

Naoyuki Inagaki

Department of Neurophysiology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan

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Masaki Inagaki

Masaki Inagaki

Department of Neurophysiology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan

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Jean-Guy Delcros

Jean-Guy Delcros

URA CNRS 1529, Faculté de Médecine, Rennes, France

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Jacques-Philippe Moulinoux

Jacques-Philippe Moulinoux

URA CNRS 1529, Faculté de Médecine, Rennes, France

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First published: 16 July 2004
Citations: 1,118

Abstract

Cyclin-dependent kinases (cdk) play an essential role in the intracellular control of the cell division cycle (cdc). These kinases and their regulators are frequently deregulated in human tumours. Enzymatic screening has recently led to the discovery of specific inhibitors of cyclin-dependent kinases, such as butyrolactone I, flavopiridol and the purine olomoucine. Among a series of C2, N6, N9-substituted ade-nines tested on purified cdc2/cylin B, 2-(1-ethyl-2-hydroxyethylamino)-6-benzylamino-9-isopropylpu-rine (roscovitine) displays high efficiency and high selectivity towards some cyclin-dependent kinases. The kinase specificity of roscovitine was investigated with 25 highly purified kinases (including protein kinase A, G and C isoforms, myosin light-chain kinase, casein kinase 2, insulin receptor tyrosine kinase, c-src, v-abl). Most kinases are not significantly inhibited by roscovitine. cdc2/cyclin B, cdk2/cyclin A, cdk2/cyclin E and cdkSlp35 only are substantially inhibited (IC50 values of 0.65, 0.7, 0.7 and 0.2 μM, respectively). cdk4/cyclin D1 and cdk6/cyclin D2 are very poorly inhibited by roscovitine (IC50>100 μM). Extracellular regulated kinases erkl and erk2 are inhibited with an IC50 of 34 μM and 14 μM, respectively. Roscovitine reversibly arrests starfish oocytes and sea urchin embryos in late pro-phase. Roscovitine inhibits in vitro M-phase-promoting factor activity and in vitro DNA synthesis in Xenopus egg extracts. It blocks progesterone-induced oocyte maturation of Xenopus oocytes and in vivo phosphorylation of the elongation factor eEF-1. Roscovitine inhibits the proliferation of mammalian cell lines with an average IC50] of 16 μM. In the presence of roscovitine L1210 cells arrest in G1 and accumulate in G2. In vivo phosphorylation of vimentin on Ser55 by cdc2/cyclin B is inhibited by roscovitine. Through its unique selectivity for some cyclin-dependent kinases, roscovitine provides a useful anti-mitotic reagent for cell cycle studies and may prove interesting to control cells with deregulated cdc2, cdk2 or cdk5 kinase activities.

Abbreviations

  • cdc
  • cell division cycle
  • cdk
  • cyclin-dependent kinase
  • erkl and erk2
  • extracellular regulated kinase 1 and 2
  • 1MeAde
  • 1-methyladenine
  • MPF
  • M-phase promoting factor
  • [Ser(P)55]vimentin
  • vimentin phosphorylated on Ser55; NCI, National Cancer Institute (USA)