Aurora-A kinase is required for centrosome maturation in Caenorhabditis elegans

被引:362
|
作者
Hannak, E
Kirkham, M
Hyman, AA
Oegema, K
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
来源
JOURNAL OF CELL BIOLOGY | 2001年 / 155卷 / 07期
关键词
microtubule; mitosis; cell cycle; cancer;
D O I
10.1083/jcb.200108051
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Centrosomes mature as cells enter mitosis, accumulating gamma -tubulin and other pericentriolar material (PCM) components. This occurs concomitant with an increase in the number of centrosomally organized microtubules (MTs). Here, we use RNA-mediated interference (RNAi) to examine the role of the aurora-A kinase, AlR-1, during centrosome maturation in Caenorhabditis elegans. In air-1(RNAi) embryos, centrosomes separate normally, an event that occurs before maturation in C. elegans. After nuclear envelope breakdown, the separated centrosomes collapse together, and spindle assembly fails. In mitotic air-1(RNAi) embryos, centrosomal alpha -tubulin fluorescence intensity accumulates to only 40% of wild-type levels, suggesting a defect in the maturation process. Consistent with this hypothesis, we find that AIR-1 is required for the increase in centrosomal gamma -tubulin and two other PCM components, ZYG-9 and CeGrip, as embryos enter mitosis. Furthermore, the AIR-1-dependent increase in centrosomal gamma -tubulin does not require MTs. These results suggest that aurora-A kinases are required to execute a MT-independent pathway for the recruitment of PCNA during centrosome maturation.
引用
收藏
页码:1109 / 1115
页数:7
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