Tirnauer J S, O'Toole E, Berrueta L, Bierer B E, Pellman D
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
J Cell Biol. 1999 May 31;145(5):993-1007. doi: 10.1083/jcb.145.5.993.
Microtubule dynamics vary during the cell cycle, and microtubules appear to be more dynamic in vivo than in vitro. Proteins that promote dynamic instability are therefore central to microtubule behavior in living cells. Here, we report that a yeast protein of the highly conserved EB1 family, Bim1p, promotes cytoplasmic microtubule dynamics specifically during G1. During G1, microtubules in cells lacking BIM1 showed reduced dynamicity due to a slower shrinkage rate, fewer rescues and catastrophes, and more time spent in an attenuated/paused state. Human EB1 was identified as an interacting partner for the adenomatous polyposis coli (APC) tumor suppressor protein. Like human EB1, Bim1p localizes to dots at the distal ends of cytoplasmic microtubules. This localization, together with data from electron microscopy and a synthetic interaction with the gene encoding the kinesin Kar3p, suggests that Bim1p acts at the microtubule plus end. Our in vivo data provide evidence of a cell cycle-specific microtubule-binding protein that promotes microtubule dynamicity.
微管动力学在细胞周期中会发生变化,而且微管在体内似乎比在体外更具动态性。因此,促进动态不稳定性的蛋白质对于活细胞中的微管行为至关重要。在此,我们报告高度保守的EB1家族的一种酵母蛋白Bim1p,特别是在G1期促进细胞质微管动力学。在G1期,缺乏BIM1的细胞中的微管由于收缩速率较慢、拯救和灾变较少以及在衰减/暂停状态花费的时间更多而表现出动态性降低。人EB1被鉴定为腺瘤性息肉病大肠杆菌(APC)肿瘤抑制蛋白的相互作用伴侣。与人类EB1一样,Bim1p定位于细胞质微管远端的小点。这种定位,连同电子显微镜数据以及与编码驱动蛋白Kar3p的基因的合成相互作用,表明Bim1p在微管正端起作用。我们的体内数据提供了一种促进微管动态性的细胞周期特异性微管结合蛋白的证据。