Centrobin-tubulin interaction is required for centriole elongation and stability

被引:52
作者
Gudi, Radhika [1 ]
Zou, Chaozhong [1 ]
Li, Jun [2 ]
Gao, Qingshen [1 ]
机构
[1] Univ Chicago, Pritzker Sch Med, NorthShore Res Inst, Dept Med, Evanston, IL 60201 USA
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Biochem, Guangzhou 510080, Guangdong, Peoples R China
基金
美国国家卫生研究院;
关键词
CYCLE-REGULATED PROTEIN; COILED-COIL PROTEIN; CENTROSOME DUPLICATION; CELL-CYCLE; C-ELEGANS; CAENORHABDITIS-ELEGANS; MAMMALIAN-CELL; KINASE; CPAP; MECHANISMS;
D O I
10.1083/jcb.201006135
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Centrobin is a daughter centriole protein that is essential for centrosome duplication. However, the molecular mechanism by which centrobin functions during centriole duplication remains undefined. In this study, we show that centrobin interacts with tubulin directly, and centrobin-tubulin interaction is pivotal for the function of centrobin during centriole duplication. We found that centrobin is recruited to the centriole biogenesis site via its interaction with tubulins during the early stage of centriole biogenesis, and its recruitment is dependent on hSAS-6 but not centrosomal P4.1-associated protein (CPAP) and CP110. The function of centrobin is also required for the elongation of centrioles, which is likely mediated by its interaction with tubulin. Furthermore, disruption of centrobin-tubulin interaction led to destabilization of existing centrioles and the preformed procentriole-like structures induced by CPAP expression, indicating that centrobin-tubulin interaction is critical for the stability of centrioles. Together, our study demonstrates that centrobin facilitates the elongation and stability of centrioles via its interaction with tubulins.
引用
收藏
页码:711 / 725
页数:15
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