Harashima Hirofumi, Kato Ko, Shinmyo Atsuhiko, Sekine Masami
Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST), Takayama 8916-5, Ikoma, Nara, Japan.
J Plant Physiol. 2007 Sep;164(9):1103-12. doi: 10.1016/j.jplph.2007.01.005. Epub 2007 Mar 13.
Although activation of A-type cyclin-dependent kinase (CDKA) is required for plant cell division, little is known about how CDKA is activated before commitment to cell division. Here, we show that auxin is required for the formation of active CDKA-associated complexes, promoting assembly of the complex in tobacco suspension culture Bright Yellow-2 (BY-2) cells. Protein gel blot analysis revealed that CDKA levels increased greatly after stationary-phase BY-2 cells were subcultured into fresh medium to re-enter the cell cycle. However, these increasing levels subsided when cells were subcultured into auxin-deprived medium, and a subtle increase was observed after subculturing into sucrose-deprived medium. Additionally, p13(suc1)-associated kinase activity did not increase significantly after subculturing into either auxin- or sucrose-deprived medium, but increased strongly after subculturing into medium containing both auxin and sucrose. Using gel filtration, we found that p13(suc1)-associated kinase activity against tobacco retinoblastoma-related protein was maximal in fractions corresponding to the molecular mass of the cyclin/CDKA complex. Interestingly, this peak distribution of high molecular-mass fractions of CDKA disappeared after cells were subcultured into auxin-deprived medium. These findings suggest an important role for auxin in the assembly of active CDKA-associated complexes.
尽管植物细胞分裂需要A类细胞周期蛋白依赖性激酶(CDKA)的激活,但对于CDKA在进入细胞分裂之前是如何被激活的,我们却知之甚少。在此,我们表明生长素是形成活性CDKA相关复合物所必需的,它能促进烟草悬浮培养的亮黄-2(BY-2)细胞中该复合物的组装。蛋白质凝胶印迹分析显示,当处于静止期的BY-2细胞被转接至新鲜培养基中重新进入细胞周期后,CDKA水平大幅增加。然而,当细胞被转接至缺乏生长素的培养基中时,这些增加的水平下降了,而转接至缺乏蔗糖的培养基中后则观察到了轻微的增加。此外,转接至缺乏生长素或蔗糖的培养基后,p13(suc1)相关激酶活性没有显著增加,但转接至同时含有生长素和蔗糖的培养基后则强烈增加。通过凝胶过滤,我们发现针对烟草视网膜母细胞瘤相关蛋白的p13(suc1)相关激酶活性在与细胞周期蛋白/CDKA复合物分子量相对应的组分中最高。有趣的是,将细胞转接至缺乏生长素的培养基后,CDKA高分子量组分的这一峰值分布消失了。这些发现表明生长素在活性CDKA相关复合物的组装中起着重要作用。