Control of the AtMAP65-1 interaction with microtubules through the cell cycle

被引:120
作者
Smertenko, Andrei P.
Chang, Hsin-Yu
Sonobe, Seiji
Fenyk, Stepan I.
Weingartner, Magdalena
Bogre, Laci
Hussey, Patrick J.
机构
[1] Univ Durham, Sch Biol & Biomed Sci, Integrat Cell Biol Lab, Durham DH1 3LE, England
[2] Himeji Inst Technol, Fac Sci, Hyogo, Japan
[3] Univ London Royal Holloway & Bedford New Coll, Sch Biol & Biomed Sci, Egham TW20 0EX, Surrey, England
基金
英国生物技术与生命科学研究理事会;
关键词
microtubule-associated protein; MAP-65; division midzone; regulation;
D O I
10.1242/jcs.03051
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell division depends on the fine control of both microtubule dynamics and microtubule organisation. The microtubule bundling protein MAP65 is a 'midzone MAP' essential for the integrity of the anaphase spindle and cell division. Arabidopsis thaliana MAP65-1 (AtMAP65-1) binds and bundles microtubules by forming 25 nm cross-bridges. Moreover, as AtMAP65-1 bundles microtubules in interphase, anaphase and telophase but does not bind microtubules in prophase or metaphase, its activity through the cell cycle must be under tight control. Here we show that AtMAP65-1 is hyperphosphorylated during prometaphase and metaphase and that CDK and MAPK are involved in this phosphorylation. This phosphorylation inhibits AtMAP65-1 activity. Expression of nonphosphorylatable AtMAP65-1 has a negative effect on mitotic progression resulting in excessive accumulation of microtubules in the metaphase spindle midzone causing a delay in mitosis. We conclude that normal metaphase spindle organisation and the transition to anaphase is dependent on inactivation of AtMAP65-1.
引用
收藏
页码:3227 / 3237
页数:11
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