Leonhard Klaus, Nurse Paul
Cancer Research UK, Cell Cycle Laboratory, 44 Lincoln's Inn Fields, London, WC2A 3PX, UK.
J Cell Sci. 2005 Mar 1;118(Pt 5):1033-44. doi: 10.1242/jcs.01690.
Polar growth is a crucial process during cell morphogenesis. The microtubule and actin cytoskeletons, and vesicular transport are tightly regulated to direct cellular growth and to generate specific cell forms. We demonstrate here that the Ste20-related protein kinase Nak1/Orb3 is required in fission yeast to polarize the actin cytoskeleton at the tips of the cells and for cell separation, and so is involved in controlling both cell shape and late stages of cytokinesis. The localization of the Nak1/Orb3 kinase to the cell tips, a medial ring and the spindle-pole bodies changes during the cell cycle, and the accumulation of F-actin at the cell tips is dependent on Nak1/Orb3 kinase. The phosphorylation of Nak1/Orb3 is periodic during the cell cycle and could be part of a mechanism that relocalizes a constitutively active kinase from the cell tips to the middle of the cell, thereby coordinating reorganization of the actin cytoskeleton and regulation of cell separation with cell-cycle progression.
极性生长是细胞形态发生过程中的一个关键过程。微管和肌动蛋白细胞骨架以及囊泡运输受到严格调控,以指导细胞生长并产生特定的细胞形态。我们在此证明,裂殖酵母中与Ste20相关的蛋白激酶Nak1/Orb3对于使肌动蛋白细胞骨架在细胞尖端极化以及细胞分离是必需的,因此参与控制细胞形状和胞质分裂的后期阶段。Nak1/Orb3激酶在细胞周期中定位于细胞尖端、中间环和纺锤极体,并且细胞尖端F-肌动蛋白的积累依赖于Nak1/Orb3激酶。Nak1/Orb3的磷酸化在细胞周期中是周期性的,可能是一种机制的一部分,该机制将组成型活性激酶从细胞尖端重新定位到细胞中部,从而协调肌动蛋白细胞骨架的重组以及细胞分离与细胞周期进程的调控。