In animal cells, duplication of centrosomes and DNA is coordinated. Since C
DK2/cyclin E triggers initiation of both events, activation of CDK2/cyclin
E is thought to link these two events. We identified nucleophosmin (NPM/B23
) as a substrate of CDK2/cyclin E in centrosome duplication. NPM/B23 associ
ates specifically with unduplicated centrosomes, and NPM/B23 dissociates fr
om centrosomes by CDK2/cyclin E-mediated phosphorylation. An anti-NPM/B23 a
ntibody, which blocks this phosphorylation, suppresses the initiation of ce
ntrosome duplication in vivo. Moreover, expression of a nonphosphorylatable
mutant NPM/ B23 in cells effectively blocks centrosome duplication. Thus,
NPM/B23 is a target of CDK2/cyclin E in the initiation of centrosome duplic
ation.