Bailly Eric, Cabantous Sandrine, Sondaz Delphine, Bernadac Alain, Simon Marie-Noelle
Laboratoire d'Ingenierie des Systemes Macromoleculaires CNRS UPR9027, 31 chemin Joseph Aiguier, 13402 Marseille Cedex 20, France.
J Cell Sci. 2003 Oct 15;116(Pt 20):4119-30. doi: 10.1242/jcs.00706.
The mitotic cyclin Clb2 plays a major role in promoting M-phase in budding yeast, despite its functional redundancy with three closely related cyclins Clb1, Clb3 and Clb4. Here, we further investigate the mechanisms controlling the cellular distribution of Clb2 in living cells. In agreement with observations recently made by Hood et al., we find that GFP-tagged Clb2 expressed from its natural promoter localizes to various cellular compartments, including the nucleus, the mitotic spindle, the spindle pole bodies as well as the mother-bud neck. The neck localization is specific to Clb2 as Clb1, Clb3 and Clb4 are never observed there, even when over-expressed. Mutational analysis identifies a central region of Clb2, comprising residues 213-255 and a phylogenetically conserved hydrophobic patch, as an essential cis-acting determinant. Clb2 co-localizes with the bud site selection protein Bud3. Consistent with a role of Bud3 in targeting Clb2 to the bud neck, we report a two-hybrid interaction between these proteins. Furthermore, Clb2 is shown to be specifically delocalized in Deltabud3 cells and in a bud3 mutant deleted for its C-terminal Clb2-interacting domain (bud3(Delta1221)), but not in a Deltabud10 mutant. Correlating with this phenotype, bud3(Delta1221) cells exhibit a pronounced (15-30 minutes) delay in cytokinesis and/or cell separation, suggesting an unanticipated function of Clb2 in these late mitotic events. Taken together, our data uncover a new role for Bud3 in cytokinesis that correlates with its capacity to target Clb2 at the neck, independently of its well established cell-type-specific function in bud site selection.
有丝分裂周期蛋白Clb2在促进芽殖酵母的M期过程中发挥着主要作用,尽管它与三种密切相关的周期蛋白Clb1、Clb3和Clb4存在功能冗余。在此,我们进一步研究了活细胞中控制Clb2细胞分布的机制。与Hood等人最近的观察结果一致,我们发现从其天然启动子表达的GFP标记的Clb2定位于各种细胞区室,包括细胞核、有丝分裂纺锤体、纺锤极体以及母-芽颈。颈定位是Clb2特有的,因为即使过表达,也从未在那里观察到Clb1、Clb3和Clb4。突变分析确定Clb2的一个中央区域,包括213 - 255位氨基酸残基和一个系统发育保守的疏水区域,是一个必需的顺式作用决定因素。Clb2与芽位选择蛋白Bud3共定位。与Bud3在将Clb2靶向芽颈中的作用一致,我们报道了这些蛋白之间的双杂交相互作用。此外,Clb2在缺失Bud3的细胞以及缺失其C端Clb2相互作用结构域(bud3(Delta1221))的芽3突变体中特异性地发生定位错误,但在缺失Bud10的突变体中没有。与这种表型相关,bud3(Delta1221)细胞在胞质分裂和/或细胞分离中表现出明显的(15 - 30分钟)延迟,这表明Clb2在这些有丝分裂后期事件中具有意想不到的功能。综上所述,我们的数据揭示了Bud3在胞质分裂中的新作用,这与其在颈部靶向Clb2的能力相关,独立于其在芽位选择中已确立的细胞类型特异性功能。