To investigate the mechanism coupling growth (protein synthesis) with cell
division, we examined the relationship between the tyrosine kinase Wee1 tha
t inhibits Cdc2-Cdc13 mitosis-inducing kinase by phosphorylating it, and pr
otein synthesis inhibition in fission yeast. The wee1-50 mutant showed supe
rsensitivity to protein synthesis inhibitor, cycloheximide, Wee1 was essent
ial for the G(2) delay upon a partial inhibition of protein synthesis. Inde
ed, the protein synthesis inhibition caused an increase in the Wee1 protein
by the Sty1/Spc1 MAPK-dependent transcriptional and the Sty1/Spc1 MAPK-ind
ependent post-transcriptional regulations. Further, the results indicated t
hat the post-transcriptional regulation is important for the G(2) delay. (C
) 2000 Federation of European Biochemical Societies, Published by Elsevier
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