Martin Sophie G, Chang Fred
Columbia University, College of Physicians and Surgeons, Department of Microbiology, New York 10032, USA.
Cell Cycle. 2005 Aug;4(8):1046-9. Epub 2005 Aug 19.
Cell polarization is a major event of the cell cycle and underlies the function of most cells. Cell polarity is often achieved through the coordinated organization of the microtubule and act in cytoskeletons. Dramatic changes in cell polarization occur during the cell cycle and are subject to regulation by cell cycle controls. Cells of the fission yeast Schizosaccharomyces pombe grow by tip extension in a cell cycle-controlled manner. During G2 phase, these cells exhibit a transition in cell polarization known as New End Take Off (NETO), in which monopolar cells initiate bipolar growth. Dynamic microtubules contribute to this process by depositing at cell ends the microtubule plus end proteins tea1p and tea4p, which are necessary for NETO. We discuss here how these proteins may recruit for 3p, a formin responsible for actin nucleation, as well as two other actin binding proteins, bud6p and sla2p, to initiate cell polarization at the new end of the cell. Thus, the study of NETO is revealing a mechanism by which the plus ends of microtubules regulate the spatial organization of actin.
细胞极化是细胞周期中的一个主要事件,是大多数细胞功能的基础。细胞极性通常通过微管的协调组织以及细胞骨架中的作用来实现。在细胞周期中,细胞极化会发生显著变化,并受到细胞周期调控的影响。裂殖酵母粟酒裂殖酵母的细胞以细胞周期控制的方式通过顶端延伸生长。在G2期,这些细胞表现出一种称为新端起始(NETO)的细胞极化转变,其中单极细胞开始双极生长。动态微管通过在细胞末端沉积微管正端蛋白tea1p和tea4p来促进这一过程,这两种蛋白是NETO所必需的。我们在此讨论这些蛋白如何招募formin 3p(一种负责肌动蛋白成核的蛋白)以及另外两种肌动蛋白结合蛋白bud6p和sla2p,以在细胞的新末端启动细胞极化。因此,对NETO的研究揭示了一种微管正端调节肌动蛋白空间组织的机制。