The Drosophila orthologue of xPlkk1 is not essential for Polo activation and is necessary for proper contractile ring formation
The Drosophila orthologue of xPlkk1 is not essential for Polo activation and is necessary for proper contractile ring formation
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DOI:
10.1016/j.yexcr.2005.10.033
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发表时间:
2006-02-01
影响因子:
3.7
通讯作者:
Tavares, AA
中科院分区:
文献类型:
--
作者:
Alves, PS;Godinho, SA;Tavares, AA
Polo-like kinases (Plks) are essential for progression through mitosis. The activity of these kinases peak during M phase and this activation has been attributed to phosphorylation. Kinases capable of activating Plks in vitro have been previously identified both in mammalian cells and in Xenopus laevis oocytes (SLK and xPIkk1, respectively), although in in vivo correlation has, not been clearly established. In order to study the regulation of Polo activity, we identified and cloned a Drosophila melanogaster kinase belonging to the ste20 ser/thr family that presents a close sequence homology with xPIkkI and SLK. We termed this kinase dPIkk and showed that dPlkk associates with and phosphorylates Polo in vitro, resulting in the activation of the latter, On the other hand, when dPIkk is depleted from S2 cells, Polo activation does not seem to be impaired, suggesting that other kinases are imolved in regulating Polo activity in vivo. Additionally, we found that a percentage of dPlkk-depleted cells fail to form a proper actin ring at the end of mitosis, leading to a failure in the assembly of the cleavage furrow and to the formation of binucleated cells. The detected accumulation of dPikk in the contractile ring late in anaphase reinforces the idea that this kinase plays a role in cytokinesis, (c) 2005 Elsevier Inc. All rights reserved.