Sawin Kenneth E, Snaith Hilary A
Wellcome Trust Centre for Cell Biology, Institute of Cell and Molecular Biology, Michael Swann Building, University of Edinburgh, Edinburgh, EH9 3JR, UK.
J Cell Sci. 2004 Feb 15;117(Pt 5):689-700. doi: 10.1242/jcs.00925. Epub 2004 Jan 20.
Microtubules and the protein tea1p have important roles in regulating cell polarity in the fission yeast Schizosaccharomyces pombe. Here, using combinations of drugs, environmental perturbations and genetic mutants, we demonstrate that once a cell polarity axis is established, microtubules have at best a minor role in maintaining the cortical actin cytoskeleton and the rate and direction of cell growth. In addition, we find that after perturbations that disrupt cell polarity and the cortical actin cytoskeleton, microtubules are not required for re-establishment of polarity per se. However, after such perturbations, the distribution of cytoplasmic microtubules plays an important role in dictating the position of sites of polarity re-establishment. Furthermore, this influence of microtubule distribution on site selection during polarity re-establishment requires the presence of tea1p, suggesting that tea1p is crucial for coupling microtubule distribution to the regulation of cell polarity. Our results suggest a model in which, at the cellular level, two distinct and separable mechanisms contribute to how tea1p regulates site selection during polarity re-establishment. First, tea1p remaining at cell tips after cortical depolarization can serve as a cortical landmark for microtubule-independent site selection; second, tea1p newly targeted to the cell cortex by association with microtubules can promote the formation of polarity axes de novo.
微管和蛋白tea1p在裂殖酵母粟酒裂殖酵母中调节细胞极性方面发挥着重要作用。在此,我们通过药物、环境扰动和基因突变体的组合,证明一旦细胞极性轴确立,微管在维持皮质肌动蛋白细胞骨架以及细胞生长速率和方向方面至多只起次要作用。此外,我们发现,在破坏细胞极性和皮质肌动蛋白细胞骨架的扰动之后,重新建立极性本身并不需要微管。然而,在这种扰动之后,细胞质微管的分布在决定极性重新建立位点的位置方面起着重要作用。此外,微管分布在极性重新建立过程中对位点选择的这种影响需要tea1p的存在,这表明tea1p对于将微管分布与细胞极性调节相耦合至关重要。我们的结果提出了一个模型,即在细胞水平上,两种不同且可分离的机制有助于tea1p在极性重新建立过程中如何调节位点选择。首先,皮质去极化后留在细胞顶端的tea1p可以作为微管非依赖性位点选择的皮质标志物;其次,通过与微管结合而新靶向到细胞皮质的tea1p可以促进从头形成极性轴。