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极光激酶通过驱动 Polo 招募纺锤体极体促进 TOR 介导的细胞周期阻滞后的细胞分裂。

Aurora promotes cell division during recovery from TOR-mediated cell cycle arrest by driving spindle pole body recruitment of Polo.

机构信息

University of Manchester, C.4255 Michael Smith Building, Faculty of Life Sciences, Oxford Road, Manchester M13 9PT, UK.

出版信息

J Cell Sci. 2011 Oct 15;124(Pt 20):3441-9. doi: 10.1242/jcs.083683. Epub 2011 Sep 29.

Abstract

The coordination of cell division and growth in response to changes in nutrient supply is mediated by TOR signalling. In fission yeast, increased nutrient provision transiently delays mitotic onset without affecting growth. The result is an increase in cell size at division. We find that this block to cell division relies upon TOR and MAPK signalling and that mitotic entry during recovery from this block is regulated by the Aurora kinase Ark1. We show that Ark1 phosphorylation of polo kinase Plo1 within the linker region between the kinase domain and polo boxes drives Plo1 onto the spindle poles where it promotes mitosis. Interestingly, the use of Ark1 to phosphorylate Plo1 and promote mitotic entry is dependent on the environment.

摘要

细胞分裂和生长的协调响应营养物质供应的变化是由 TOR 信号介导的。在裂殖酵母中,增加营养物质的供应会短暂地延迟有丝分裂的开始,而不影响生长。其结果是细胞在分裂时的体积增加。我们发现,这种细胞分裂的阻断依赖于 TOR 和 MAPK 信号,并且在从这种阻断中恢复时的有丝分裂进入是由 Aurora 激酶 Ark1 调节的。我们表明,Ark1 在激酶结构域和 polo 盒之间的连接区对 polo 激酶 Plo1 的磷酸化将 Plo1 驱动到纺锤体极上,在那里它促进有丝分裂。有趣的是,Ark1 用于磷酸化 Plo1 并促进有丝分裂进入的作用依赖于环境。

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