Beatson Institute for Cancer Research, Garscube Estate, Switchback Road, Bearsden, Glasgow G61 1BD, UK.
Mol Cell. 2012 Feb 24;45(4):541-52. doi: 10.1016/j.molcel.2011.11.030. Epub 2012 Jan 25.
Polo-like kinase Plk1 controls numerous aspects of cell-cycle progression. We show that it associates with tRNA and 5S rRNA genes and regulates their transcription by RNA polymerase III (pol III) through direct binding and phosphorylation of transcription factor Brf1. During interphase, Plk1 promotes tRNA and 5S rRNA expression by phosphorylating Brf1 directly on serine 450. However, this stimulatory modification is overridden at mitosis, when elevated Plk1 activity causes Brf1 phosphorylation on threonine 270 (T270), which prevents pol III recruitment. Thus, although Plk1 enhances net tRNA and 5S rRNA production, consistent with its proliferation-stimulating function, it also suppresses untimely transcription when cells divide. Genomic instability is apparent in cells with Brf1 T270 mutated to alanine to resist Plk1-directed inactivation, suggesting that chromosome segregation is vulnerable to inappropriate pol III activity.
丝氨酸苏氨酸激酶 Plk1 控制细胞周期进程的许多方面。我们表明它与 tRNA 和 5S rRNA 基因相关,并通过 RNA 聚合酶 III(pol III)直接结合和磷酸化转录因子 Brf1 来调节它们的转录。在间期,Plk1 通过直接在丝氨酸 450 上磷酸化 Brf1 来促进 tRNA 和 5S rRNA 的表达。然而,这种刺激修饰在有丝分裂时被掩盖,此时升高的 Plk1 活性导致 Brf1 在苏氨酸 270 上的磷酸化(T270),从而阻止 pol III 的募集。因此,尽管 Plk1 增强了净 tRNA 和 5S rRNA 的产生,与它的增殖刺激功能一致,但当细胞分裂时,它也会抑制不合时宜的转录。在 Brf1 的苏氨酸 270 突变为丙氨酸以抵抗 Plk1 介导的失活的细胞中,明显存在基因组不稳定性,这表明染色体分离容易受到不当的 pol III 活性的影响。