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Large tumor suppressors 1 and 2 regulate Aurora-B through phosphorylation of INCENP to ensure completion of cytokinesis

机译:大型肿瘤抑制因子1和2通过INCENP的磷酸化调节Aurora-B以确保完成胞质分裂

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摘要

The tumor suppressor kinases LATS1 and LATS2 (LATS1/2) regulate not only organ size through the Hippo signaling pathway, but also cell-cycle checkpoints and apoptosis via other signaling cascades. We previously reported that LATS1/2 localize to the mitotic apparatus, where they are involved in the phosphorylation and activation of the mitotic kinase Aurora-B; however, the detailed mechanism of LATS1/2 action remains obscure. The activity of Aurora-B is stringently regulated by formation of the chromosomal passenger complex containing the inner centromere protein (INCENP), which leads to appropriate activation of Aurora-B during mitosis and cytokinesis. In this study, we found that LATS1/2 phosphorylated INCENP at S894 in the Thr-Ser-Ser motif. Moreover, the LATS-mediated phosphorylation of S894 was necessary and sufficient for the activation of Aurora-B, which is required for completion of cytokinesis in cells engaged in multipolar division. We propose a novel mechanism for regulation of Aurora-B via INCENP phosphorylation by LATS1/2 during cytokinesis.
机译:肿瘤抑制激酶LATS1和LATS2(LATS1 / 2)不仅通过Hippo信号通路调节器官大小,而且还通过其他信号级联调节细胞周期检查点和凋亡。我们以前曾报道过LATS1 / 2定位于有丝分裂装置,在该处它们参与有丝分裂激酶Aurora-B的磷酸化和激活。但是,LATS1 / 2作用的详细机制仍然不清楚。 Aurora-B的活性受到包含内部着丝粒蛋白(INCENP)的染色体乘客复合物的形成的严格调控,这导致Aurora-B在有丝分裂和胞质分裂过程中被适当激活。在这项研究中,我们发现LATS1 / 2在Thr-Ser-Ser主题的S894处磷酸化了INCENP。此外,LATS介导的S894磷酸化对于激活Aurora-B是必需的,而Aurora-B的激活对于完成参与多极分裂的细胞的胞质分裂是必需的。我们提出了一种新的机制,通过胞质分裂过程中LATS1 / 2通过INCENP磷酸化调节Aurora-B。

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