Hutterer Andrea, Berdnik Daniela, Wirtz-Peitz Frederik, Zigman Mihaela, Schleiffer Alexander, Knoblich Juergen A
Institute of Molecular Biotechnology (IMBA), Dr Bohr Gasse 3-5, 1030 Vienna, Austria.
Dev Cell. 2006 Aug;11(2):147-57. doi: 10.1016/j.devcel.2006.06.002.
The protein kinase Aurora-A is required for centrosome maturation, spindle assembly, and asymmetric protein localization during mitosis. Here, we describe the identification of Bora, a conserved protein that is required for the activation of Aurora-A at the onset of mitosis. In the Drosophila peripheral nervous system, bora mutants have defects during asymmetric cell division identical to those observed in aurora-A. Furthermore, overexpression of bora can rescue defects caused by mutations in aurora-A. Bora is conserved in vertebrates, and both Drosophila and human Bora can bind to Aurora-A and activate the kinase in vitro. In interphase cells, Bora is a nuclear protein, but upon entry into mitosis, Bora is excluded from the nucleus and translocates into the cytoplasm in a Cdc2-dependent manner. We propose a model in which activation of Cdc2 initiates the release of Bora into the cytoplasm where it can bind and activate Aurora-A.
蛋白激酶Aurora-A在有丝分裂期间对于中心体成熟、纺锤体组装及不对称蛋白定位是必需的。在此,我们描述了Bora的鉴定,Bora是一种保守蛋白,在有丝分裂开始时对于Aurora-A的激活是必需的。在果蝇外周神经系统中,bora突变体在不对称细胞分裂过程中具有与在Aurora-A中观察到的相同的缺陷。此外,bora的过表达可以挽救由Aurora-A突变引起的缺陷。Bora在脊椎动物中是保守的,果蝇和人类的Bora都能与Aurora-A结合并在体外激活该激酶。在间期细胞中,Bora是一种核蛋白,但进入有丝分裂后,Bora被排除在细胞核外,并以依赖Cdc2的方式转运到细胞质中。我们提出了一个模型,其中Cdc2的激活引发Bora释放到细胞质中,在那里它可以结合并激活Aurora-A。