Plk1 regulates mitotic Aurora A function through betaTrCP-dependent degradation of hBora

Polo-like kinase 1 (PLK1) and Aurora A play key roles in centrosome maturation, spindle assembly, and chromosome segregation during cell division. Here we show that the functions of these kinases during early mitosis are coordinated through Bora, a partner of Aurora A first identified in Drosophila. Depletion of human Bora (hBora) results in spindle defects, accompanied by increased spindle recruitment of Aurora A and its partner TPX2. Conversely, hBora overexpression induces mislocalization of Aurora A and monopolar spindle formation, reminiscent of the phenotype seen in Plk1-depleted cells. Indeed, PLK1 regulates hBora. Following Cdk1-dependent recruitment, PLK1 triggers hBora destruction by phosphorylating a recognition site for SCF(Beta-TrCP). PLK1 depletion or inhibition results in a massive accumulation of hBora, concomitant with displacement of Aurora A from spindle poles and impaired centrosome maturation, but remarkably, co-depletion of hBora partially restores Aurora A localization and bipolar spindle formation. This suggests that PLK1 controls Aurora A localization and function by regulating cellular levels of hBora.