G Protein-coupled Receptor Kinase 5 Is Localized to Centrosomes and Regulates Cell Cycle Progression

被引:32
作者
Michal, Allison M. [1 ]
So, Christopher H. [1 ]
Beeharry, Neil [2 ]
Shankar, Haripriya [1 ]
Mashayekhi, Rouzbeh [1 ]
Yen, Timothy J. [2 ]
Benovic, Jeffrey L. [1 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[2] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
基金
美国国家卫生研究院;
关键词
POLO-LIKE KINASE-1; AURORA-A; NUCLEAR-LOCALIZATION; PHOSPHORYLATION; ARRESTINS; MEMBRANE; DIVISION; TUBULIN; GRK2; TRAFFICKING;
D O I
10.1074/jbc.M111.298034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptor kinases (GRKs) are important regulators of G protein-coupled receptor function and mediate receptor desensitization, internalization, and signaling. While GRKs also interact with and/or phosphorylate many other proteins and modify their function, relatively little is known about the cellular localization of endogenous GRKs. Here we report that GRK5 co-localizes with gamma-tubulin, centrin, and pericentrin in centrosomes. The centrosomal localization of GRK5 is observed predominantly at interphase and although its localization is not dependent on microtubules, it can mediate microtubule nucleation of centrosomes. Knockdown of GRK5 expression leads to G2/M arrest, characterized by a prolonged G2 phase, which can be rescued by expression of wild type but not catalytically inactive GRK5. This G2/ M arrest appears to be due to increased expression of p53, reduced activity of aurora A kinase and a subsequent delay in the activation of polo-like kinase 1. Overall, these studies demonstrate that GRK5 is localized in the centrosome and regulates microtubule nucleation and normal cell cycle progression.
引用
收藏
页码:6928 / 6940
页数:13
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