DNA-replication/DNA-damage-dependent centrosome inactivation in Drosophila embryos

被引:132
作者
Sibon, OCM
Kelkar, A
Lemstra, W
Theurkauf, WE
机构
[1] Univ Massachusetts, Med Ctr, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Groningen, Dept Radiobiol, Fac Med, Groningen, Netherlands
[3] Univ Massachusetts, Med Ctr, Dept Mol Genet & Microbiol, Worcester, MA 01605 USA
关键词
D O I
10.1038/35000041
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During early embryogenesis of Drosophila melanogaster, mutations in the DNA-replication checkpoint lead to chromosome-segregation failures. Here we show that these segregation failures are associated with the assembly of an anastral microtubule spindle, a mitosis-specific loss of centrosome function, and dissociation of several components of the gamma-tubulin ring complex from a core centrosomal structure. The DNA-replication inhibitor aphidicolin and DNA-damaging agents trigger identical mitotic defects in wild-type embryos, indicating that centrosome inactivation is a checkpoint-independent and mitosis-specific response to damaged or incompletely replicated DNA, We propose that centrosome inactivation is part of a damage-control system that blocks chromosome segregation when replication/damage checkpoint control fails.
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收藏
页码:90 / 95
页数:6
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