Nucleophosmin/B23 is a target of CDK2/Cyclin E in centrosome duplication

Citation
M. Okuda et al., Nucleophosmin/B23 is a target of CDK2/Cyclin E in centrosome duplication, CELL, 103(1), 2000, pp. 127-140
Citations number
38
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL
ISSN journal
00928674 → ACNP
Volume
103
Issue
1
Year of publication
2000
Pages
127 - 140
Database
ISI
SICI code
0092-8674(20000929)103:1<127:NIATOC>2.0.ZU;2-6
Abstract
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.