Lee K S, Song S, Erikson R L
Laboratory of Metabolism, Division of Basic Sciences, National Cancer Institute, National Institutes of Health, 9000 Rockville Pike, Building 37, Room 3D25, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 1999 Dec 7;96(25):14360-5. doi: 10.1073/pnas.96.25.14360.
Members of the polo subfamily of protein kinases play pivotal roles in cell-cycle control and proliferation. In addition to a high degree of sequence similarity in the kinase domain, polo kinases contain a strikingly conserved motif termed "polo-box" in the noncatalytic C-terminal domain. We have previously shown that the mammalian polo-like kinase Plk is a functional homolog of Saccharomyces cerevisiae Cdc5. Here, we show that, in a polo-box- and kinase activity-dependent manner, ectopic expression of Plk in budding yeast can induce a class of cells with abnormally elongated buds. In addition to localization at spindle poles and cytokinetic neck filaments, Plk induces and localizes to ectopic septin ring structures within the elongated buds. In contrast, mutations in the polo-box abolish both localization to, and induction of, septal structures. Consistent with the polo-box-dependent subcellular localization, the C-terminal domain of Plk, but not its polo-box mutant, is sufficient for subcellular localization. Our data suggest that Plk may contribute a signal to initiate or promote cytokinetic event(s) and that an intact polo-box is required for regulation of these cellular processes.
蛋白激酶polo亚家族的成员在细胞周期调控和增殖中发挥着关键作用。除了激酶结构域具有高度的序列相似性外,polo激酶在非催化性的C末端结构域还含有一个显著保守的基序,称为“polo框”。我们之前已经表明,哺乳动物的polo样激酶Plk是酿酒酵母Cdc5的功能同源物。在此,我们表明,以一种依赖于polo框和激酶活性的方式,在芽殖酵母中异位表达Plk可诱导产生一类芽异常伸长的细胞。除了定位于纺锤极和胞质分裂颈部细丝外,Plk还诱导并定位于伸长芽内的异位隔膜蛋白环结构。相反,polo框中的突变消除了对隔膜结构的定位和诱导。与依赖于polo框的亚细胞定位一致,Plk的C末端结构域而非其polo框突变体足以进行亚细胞定位。我们的数据表明,Plk可能有助于启动或促进胞质分裂事件,并且完整的polo框对于这些细胞过程的调控是必需的。