Abstract

Aurora B kinase is an essential regulator of chromosome segregation with the action well characterized in eukaryotes. It is also implicated in cytokinesis, but the detailed mechanism remains less clear, partly due to the difficulty in separating the latter from the former function in a growing cell. A chemical genetic approach with an inhibitor of the enzyme added to a synchronized cell population at different stages of the cell cycle would probably solve this problem. In the deeply branched parasitic protozoan Trypanosoma brucei, an Aurora B homolog, TbAUK1, was found to control both chromosome segregation and cytokinetic initiation by evidence from RNAi and dominant negative mutation. To clearly separate these two functions, VX-680, an inhibitor of TbAUK1, was added to a synchronized T. brucei procyclic cell population at different cell cycle stages. The unique trans-localization pattern of the chromosomal passenger complex (CPC), consisting of TbAUK1 and two novel proteins TbCPC1 and TbCPC2, was monitored during mitosis and cytokinesis by following the migration of the proteins tagged with enhanced yellow fluorescence protein in live cells with time-lapse video microscopy. Inhibition of TbAUK1 function in S-phase, prophase or metaphase invariably arrests the cells in the metaphase, suggesting an action of TbAUK1 in promoting metaphase-anaphase transition. TbAUK1 inhibition in anaphase does not affect mitotic exit, but prevents trans-localization of the CPC from the spindle midzone to the anterior tip of the new flagellum attachment zone for cytokinetic initiation. The CPC in the midzone is dispersed back to the two segregated nuclei, while cytokinesis is inhibited. In and beyond telophase, TbAUK1 inhibition has no effect on the progression of cytokinesis or the subsequent G1, S and G2 phases until a new metaphase is attained. There are thus two clearly distinct points of TbAUK1 action in T. brucei: the metaphase-anaphase transition and cytokinetic initiation. This is the first time to our knowledge that the dual functions of an Aurora B homolog is dissected and separated into two clearly distinct time frames in a cell cycle.

Highlights

  • The Aurora-like kinases are essential mitotic regulators among eukaryotes

  • The chromosomal passenger complex (CPC) in Trypanosoma brucei consists of an Aurora-like kinase (TbAUK1) and two novel proteins and bears little resemblance to the CPC in other eukaryotes

  • We demonstrated that TbAUK1 plays essential roles at two distinctive stages of the cell cycle; (1) the metaphase-anaphase transition; (2) the trans-localization of the CPC from the spindle midzone to the dorsal anterior of the cell at the beginning of cytokinesis

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Summary

Introduction

The Aurora-like kinases are essential mitotic regulators among eukaryotes. In metazoa, there are three such enzymes; Aurora A regulating spindle assembly, Aurora B promoting chromosome segregation and cytokinesis and Aurora C controlling chromosome segregation during male meiosis. Only a single Aurora-like kinase is required in budding and fission yeasts for spindle assembly and chromosome segregation without an apparent involvement in cytokinesis (for a review, see [1]). The single Aurora-like kinase Ipl1p forms a CPC with three homologs of INCENP (Sli15p), Survivin (Bir1p) and Borealin (Nbl1p) [5,6]. The mechanisms of CPC in detecting and correcting aberrant kinetochore-microtubule attachments during mitosis have been well characterized in yeast and metazoa These involve the phosphorylation of several key kinetochore components by Aurora B [7,8,9,10,11], the activation of spindle checkpoint by targeting the checkpoint components to kinetochores [12] and the promotion of the association of BUBR1 with the anaphasepromoting complex/cyclosome (APC/C) [13]. The components of the kinetochore and the spindle checkpoint as well as the regulatory pathways governing kinetochore-microtubule attachments and chromosome segregation are well conserved from yeast to human

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