Unit of Cellular Networks and Molecular Therapeutic Targets, Regina Elena National Cancer Institute-IRCCS, Rome, 00144, Italy.
Institute of Molecular Biology and Pathology (IBPM), National Research Council (CNR), c/o Sapienza University, Rome, 00185, Italy.
Oncogene. 2018 Jun;37(26):3562-3574. doi: 10.1038/s41388-018-0191-6. Epub 2018 Mar 22.
Cytokinesis, the final phase of cell division, is necessary to form two distinct daughter cells with correct distribution of genomic and cytoplasmic materials. Its failure provokes genetically unstable states, such as tetraploidization and polyploidization, which can contribute to tumorigenesis. Aurora-B kinase controls multiple cytokinetic events, from chromosome condensation to abscission when the midbody is severed. We have previously shown that HIPK2, a kinase involved in DNA damage response and development, localizes at the midbody and contributes to abscission by phosphorylating extrachromosomal histone H2B at Ser14. Of relevance, HIPK2-defective cells do not phosphorylate H2B and do not successfully complete cytokinesis leading to accumulation of binucleated cells, chromosomal instability, and increased tumorigenicity. However, how HIPK2 and H2B are recruited to the midbody during cytokinesis is still unknown. Here, we show that regardless of their direct (H2B) and indirect (HIPK2) binding of chromosomal DNA, both H2B and HIPK2 localize at the midbody independently of nucleic acids. Instead, by using mitotic kinase-specific inhibitors in a spatio-temporal regulated manner, we found that Aurora-B kinase activity is required to recruit both HIPK2 and H2B to the midbody. Molecular characterization showed that Aurora-B directly binds and phosphorylates H2B at Ser32 while indirectly recruits HIPK2 through the central spindle components MgcRacGAP and PRC1. Thus, among different cytokinetic functions, Aurora-B separately recruits HIPK2 and H2B to the midbody and these activities contribute to faithful cytokinesis.
有丝分裂是细胞分裂的最后一个阶段,对于形成两个具有正确基因组和细胞质物质分配的独特子细胞是必要的。它的失败会引发遗传不稳定状态,如四倍体化和多倍体化,这可能导致肿瘤发生。Aurora-B 激酶控制着多个有丝分裂事件,从染色体浓缩到中体被切断时的分裂。我们之前已经表明,参与 DNA 损伤反应和发育的激酶 HIPK2 定位于中体,并通过磷酸化染色体外组蛋白 H2B 的丝氨酸 14 位来促进分裂。相关的是,HIPK2 缺陷细胞不会磷酸化 H2B,并且不能成功完成有丝分裂,导致双核细胞的积累、染色体不稳定和肿瘤形成性增加。然而,HIPK2 和 H2B 在有丝分裂期间如何被招募到中体仍然未知。在这里,我们表明,无论它们直接(H2B)和间接(HIPK2)结合染色体 DNA,H2B 和 HIPK2 都独立于核酸定位在中体上。相反,通过在时空上有规律地使用有丝分裂激酶特异性抑制剂,我们发现 Aurora-B 激酶活性是将 HIPK2 和 H2B 招募到中体所必需的。分子特征表明,Aurora-B 直接结合并磷酸化 H2B 的丝氨酸 32 位,同时通过中心纺锤体组件 MgcRacGAP 和 PRC1 间接招募 HIPK2。因此,在不同的有丝分裂功能中,Aurora-B 分别将 HIPK2 和 H2B 招募到中体,这些活性有助于有丝分裂的忠实进行。