Mitotic Regulation of the Stability of Microtubule Plus-end Tracking Protein EB3 by Ubiquitin Ligase SIAH-1 and Aurora Mitotic Kinases

被引:45
作者
Ban, Reiko [1 ,2 ]
Matsuzaki, Hideki [4 ]
Akashi, Tomohiro [3 ]
Sakashita, Gyosuke [1 ,2 ]
Taniguchi, Hisaaki [4 ]
Park, Sam-Yong [5 ]
Tanaka, Hirofumi [6 ]
Furukawa, Koichi [2 ]
Urano, Takeshi [1 ,2 ]
机构
[1] Shimane Univ, Dept Biochem, Sch Med, Izumo, Shimane 6938501, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Biochem, Nagoya, Aichi 4668550, Japan
[3] Nagoya Univ, Grad Sch Med, Div Mol Mycol & Med, Nagoya, Aichi 4668550, Japan
[4] Univ Tokushima, Inst Enzyme Res, Tokushima 7708503, Japan
[5] Yokohama City Univ, Prot Design Lab, Yokohama, Kanagawa 2300045, Japan
[6] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Tokyo 1920392, Japan
关键词
INHIBITS CELL-GROWTH; NEGATIVE REGULATORS; BINDING-PROTEINS; SPINDLE; ACTIVATION; DYNAMICS; MITOSIS; PHOSPHORYLATION; DEGRADATION; APC;
D O I
10.1074/jbc.M109.000273
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
Microtubule plus-end tracking proteins (+TIPs) control microtubule dynamics in fundamental processes such as cell cycle, intracellular transport, and cell motility, but how +TIPs are regulated during mitosis remains largely unclear. Here we show that the endogenous end-binding protein family EB3 is stable during mitosis, facilitates cell cycle progression at prometaphase, and then is down-regulated during the transition to G, phase. The ubiquitin-protein isopeptide ligase SIAH-1 facilitates EB3 polyubiquitination and subsequent proteasome-mediated degradation, whereas SIAH-1 knockdown increases EB3 stability and steady-state levels. Two mitotic kinases, Aurora-A and Aurora-B, phosphorylate endogenous EB3 at Ser-176, and the phosphorylation triggers disruption of the EB3-SIAH-1 complex, resulting in EB3 stabilization during mitosis. Our results provide new insight into a regulatory mechanism of +TIPs in cell cycle transition.
引用
收藏
页码:28367 / 28381
页数:15
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