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A novel role for TPX2 as a scaffold and co-activator protein of the Chromosomal Passenger Complex

机译:TPX2作为TPX2作为染色体乘客综合体的支架和共激活蛋白的新作用

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摘要

Aurora B kinase forms the enzymatic core of the Chromosomal Passenger Complex (CPC) and is a master regulator of mitosis. Understanding the regulation of Aurora B is critical to illuminate its role in mitosis. INCENP, Survivin and Borealin have all been known to promote Aurora B activation. In this study, we have identified the Aurora A activator protein TPX2 as a novel scaffold and co-activator protein of the CPC. Studies utilizing M-phase Xenopus egg extracts (XEE) revealed that the immunodepletion of endogenous TPX2 from XEE decreases Aurora B-Survivin and Aurora B-INCENP interactions, leading to a consequent reduction in Aurora B activity. Further, residues 138 to 328 of Xenopus TPX2 (TPX2 B) are sufficient to enhance Aurora B-Survivin association and Aurora B kinase activity in vitro. Importantly, experiments with pancreatic cancer cell lines suggest that this mechanism of Aurora B activation by TPX2 is likely to be conserved in human cells. Strikingly, the overexpression of human TPX2 B in HeLa cells causes defects in metaphase chromosome alignment and INCENP localization. Thus, in addition to its already established role as an Aurora A activator, our data support the role of TPX2 as a novel co-activator of Aurora kinase B.
机译:Aurora B激酶形成染色体乘客综合体(CPC)的酶核心,是有丝分裂的常规调节剂。了解极光法的调节对于照亮其在有丝分裂中的作用至关重要。所有人都众所周知,Survivin和Borealin都促进了Aurora B激活。在这项研究中,我们已经将Aurora鉴定为CPC的新型支架和共振蛋白的激活剂蛋白TPX2。利用M相Xenopus蛋提取物(Xee)的研究表明,XEE的内源性TPX2免疫刻度降低了极罗拉B-Survivin和极光B-Invenp的相互作用,导致极光B活性降低。此外,Xenopus TPX2(TPX2b)的残基138至328足以在体外增强Aurora B-Survivin关联和极光B激酶活性。重要的是,胰腺癌细胞系的实验表明,TPX2的Aurora B激活的这种机制可能在人体细胞中被保守。引人注目的是,HeLa细胞中人TPX2b的过表达导致中期染色体对准和INVENCP定位中的缺陷。因此,除了它已经建立的作为Aurora激活因子的角色外,我们的数据还支持TPX2作为Aurora激酶B的新型共激活剂的作用。

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