Department of Biochemistry, Ajou University School of Medicine, Suwon 443-721 Korea; Graduate School of Molecular Science and Technology, Ajou University, Suwon 443-721 Korea.
B Cell Molecular Immunology Section, Laboratory of Immunoregulation, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 2011 Sep 2;286(35):30615-30623. doi: 10.1074/jbc.M111.231803. Epub 2011 Jul 15.
The E3 ubiquitin-protein ligase Chfr is a mitotic stress checkpoint protein that delays mitotic entry in response to microtubule damage; however, the molecular mechanism by which Chfr accomplishes this remains elusive. Here, we show that Chfr levels are elevated in response to microtubule-damaging stress. Moreover, G(2)/M transition is associated with cell cycle-dependent turnover of Chfr accompanied by high autoubiquitylation activity, suggesting that regulation of Chfr levels and auto-ubiquitylation activity are functionally significant. To test this, we generated Chfr mutants Chfr-K2A and Chfr-K5A in which putative lysine target sites of auto-ubiquitylation were replaced with alanine. Chfr-K2A did not undergo cell cycle-dependent degradation, and its levels remained high during G(2)/M phase. The elevated levels of Chfr-K2A caused a significant reduction in phosphohistone H3 levels and cyclinB1/Cdk1 kinase activities, leading to mitotic entry delay. Notably, polo-like kinase 1 levels at G(2) phase, but not at S phase, were ∼2-3-fold lower in cells expressing Chfr-K2A than in wild-type Chfr-expressing cells. Consistent with this, ubiquitylation of Plk1 at G(2) phase was accelerated in Chfr-K2A-expressing cells. In contrast, Aurora A levels remained constant, indicating that Plk1 is a major target of Chfr in controlling the timing of mitotic entry. Indeed, overexpression of Plk1 in Chfr-K2A-expressing cells restored cyclin B1/Cdk1 kinase activity and promoted mitotic entry. Collectively, these data indicate that Chfr auto-ubiquitylation is required to allow Plk1 to accumulate to levels necessary for activation of cyclin B1/Cdk1 kinase and mitotic entry. Our results provide the first evidence that Chfr auto-ubiquitylation and degradation are important for the G(2)/M transition.
E3 泛素蛋白连接酶 Chfr 是有丝分裂应激检查点蛋白,可响应微管损伤延迟有丝分裂进入;然而,Chfr 完成此任务的分子机制仍不明确。在这里,我们发现 Chfr 水平响应微管损伤应激而升高。此外,G2/M 期转换与 Chfr 的细胞周期依赖性周转有关,伴有高自泛素化活性,表明 Chfr 水平和自泛素化活性的调节具有功能意义。为了验证这一点,我们生成了 Chfr 突变体 Chfr-K2A 和 Chfr-K5A,其中自泛素化的假定赖氨酸靶位被替换为丙氨酸。Chfr-K2A 没有经历细胞周期依赖性降解,并且在 G2/M 期其水平仍然很高。Chfr-K2A 的高水平导致磷酸组蛋白 H3 水平和细胞周期蛋白 B1/Cdk1 激酶活性显著降低,导致有丝分裂进入延迟。值得注意的是,表达 Chfr-K2A 的细胞中 polo 样激酶 1(Plk1)的水平在 G2 期而非 S 期比表达野生型 Chfr 的细胞低约 2-3 倍。与此一致,Chfr-K2A 表达细胞中的 Plk1 在 G2 期的泛素化加速。相比之下,Aurora A 水平保持不变,表明 Plk1 是 Chfr 控制有丝分裂进入时间的主要靶标。事实上,在 Chfr-K2A 表达细胞中过表达 Plk1 恢复了细胞周期蛋白 B1/Cdk1 激酶活性并促进了有丝分裂进入。总的来说,这些数据表明 Chfr 自泛素化对于 Plk1 积累到激活细胞周期蛋白 B1/Cdk1 激酶和有丝分裂进入所需的水平是必需的。我们的结果首次表明 Chfr 自泛素化和降解对于 G2/M 期转换很重要。