Pruyne D, Bretscher A
Department of Molecular Biology, Cornell University, Ithaca, NY 14853, USA.
J Cell Sci. 2000 Feb;113 ( Pt 4):571-85. doi: 10.1242/jcs.113.4.571.
The actin cytoskeleton provides the structural basis for cell polarity in Saccharomyces cerevisiae as well as most other eukaryotes. In Part I of this two-part commentary, presented in the previous issue of Journal of Cell Science, we discussed the basis by which yeast establishes and maintains different states of polarity through &Rgr; GTPases and cyclin-dependent protein kinase signaling. Here we discuss how, in response to those signals, the actin cytoskeleton guides growth of the yeast cell. A polarized array of actin cables at the cell cortex is the primary structural determinant of polarity. Motors such as class V myosins use this array to transport secretory vesicles, mRNA and organelles towards growth sites, where they are anchored by a cap of cytoskeletal and regulatory proteins. Cortical actin patches enhance and maintain this polarity, probably through endocytic recycling, which allows reuse of materials and prevents continued growth at old sites. The dynamic arrangement of targeting and recycling provides flexibility for the precise control of morphogenesis.
肌动蛋白细胞骨架为酿酒酵母以及大多数其他真核生物的细胞极性提供了结构基础。在本期《细胞科学杂志》上发表的这篇两部分评论的第一部分中,我们讨论了酵母通过Rho GTP酶和细胞周期蛋白依赖性蛋白激酶信号传导建立和维持不同极性状态的基础。在这里,我们讨论肌动蛋白细胞骨架如何响应这些信号来引导酵母细胞的生长。细胞皮层处极化排列的肌动蛋白电缆是极性的主要结构决定因素。诸如V类肌球蛋白之类的马达利用这种排列将分泌囊泡、mRNA和细胞器运输到生长位点,在那里它们由细胞骨架和调节蛋白的帽固定。皮层肌动蛋白斑可能通过胞吞循环增强并维持这种极性,胞吞循环允许材料的再利用并防止在旧位点持续生长。靶向和循环的动态安排为形态发生的精确控制提供了灵活性。