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

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<jats:p>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, N<jats:sup>6</jats:sup>, 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 (IC<jats:sub>50</jats:sub> 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 (IC<jats:sub>50</jats:sub>>100 μM). Extracellular regulated kinases erkl and erk2 are inhibited with an IC<jats:sub>50</jats:sub> of 34 μM and 14 μM, respectively. Roscovitine reversibly arrests starfish oocytes and sea urchin embryos in late pro‐phase. Roscovitine inhibits <jats:italic>in vitro</jats:italic> M‐phase‐promoting factor activity and <jats:italic>in vitro</jats:italic> DNA synthesis in <jats:italic>Xenopus</jats:italic> egg extracts. It blocks progesterone‐induced oocyte maturation of <jats:italic>Xenopus</jats:italic> oocytes and <jats:italic>in vivo</jats:italic> phosphorylation of the elongation factor eEF‐1. Roscovitine inhibits the proliferation of mammalian cell lines with an average IC<jats:sub>50</jats:sub>] of 16 μM. In the presence of roscovitine L1210 cells arrest in G1 and accumulate in G2. <jats:italic>In vivo</jats:italic> 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.</jats:p>

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