Inhibition of centrosome separation after DNA damage: A role for Nek2

被引:74
作者
Fletcher, L
Cerniglia, GJ
Nigg, EA
Yen, TJ
Muschel, RJ
机构
[1] Childrens Hosp Philadelphia, Dept Pathol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[3] Max Planck Inst Biochem, Dept Cell Biol, D-82152 Martinsried, Germany
[4] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
关键词
D O I
10.1667/RR3211
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA damage results in cell cycle arrest in G, Centrosomes also separate in G2, raising the question of whether separation occurs during the DNA damage-induced G2 arrest. Nek2, the mammalian homologue of NIMA, is a cell cycle-regulated serine/threonine protein kinase that regulates centrosome separation during G2. Here we show that damaged cells fail to activate Nek2. Both Nek2 levels and activity are reduced after DNA damage. Radiation inhibits the premature centrosome splitting induced by overexpression of Nek2, indicating that Nek2 is involved in activation of the G, checkpoint and is not secondary to cell cycle arrest. We confirm using siRNA that centrosome separation and cell growth are impaired in the absence of Nek2. These studies define a previously unreported DNA damage response of inhibition of centrosome separation mechanistically linked to Nek2. (C) 2004 by Radiation Research Society.
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页码:128 / 135
页数:8
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