Cell cycle progression is dependent on the sequential activity of cyclin-de
pendent kinases (CDKs), For full activity, CDKs require an activating phosp
horylation of a conserved residue (corresponding to Thr160 in human CDK2) c
arried out by the CDK-activating kinase (CAK), Two distinct CAK kinases hav
e been described: in budding yeast Saccharomyces cerevisiae, the Cak1/Civ1
kinase is responsible for CAK activity. In several other species including
human, Xenopus, Drosophila and fission yeast Schizosaccharomyces pombe, CAK
has been identified as a complex homologous to CDK7-cyclin H (Mcs6-Mcs2 in
fission yeast). Here we identify the fission yeast Csk1 kinase as an in vi
vo activating kinase of the Mcs6-Mcs2 CAK defining Csk1 as a CAK-activating
kinase (CAKAK).