Kitamura Etsushi, Tanaka Kozo, Kitamura Yoko, Tanaka Tomoyuki U
Wellcome Trust Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee, Dundee DD1 5EH, United Kingdom.
Genes Dev. 2007 Dec 15;21(24):3319-30. doi: 10.1101/gad.449407.
In the budding yeast Saccharomyces cerevisiae, microtubule-organizing centers called spindle pole bodies (SPBs) are embedded in the nuclear envelope, which remains intact throughout the cell cycle (closed mitosis). Kinetochores are tethered to SPBs by microtubules during most of the cell cycle, including G1 and M phases; however, it has been a topic of debate whether microtubule interaction is constantly maintained or transiently disrupted during chromosome duplication. Here, we show that centromeres are detached from microtubules for 1-2 min and displaced away from a spindle pole in early S phase. These detachment and displacement events are caused by centromere DNA replication, which results in disassembly of kinetochores. Soon afterward, kinetochores are reassembled, leading to their recapture by microtubules. We also show how kinetochores are subsequently transported poleward by microtubules. Our study gives new insights into kinetochore-microtubule interaction and kinetochore duplication during S phase in a closed mitosis.
在出芽酵母酿酒酵母中,被称为纺锤体极体(SPB)的微管组织中心嵌入核膜,核膜在整个细胞周期(封闭有丝分裂)中保持完整。在细胞周期的大部分时间,包括G1期和M期,动粒通过微管与纺锤体极体相连;然而,在染色体复制过程中,微管相互作用是持续维持还是短暂中断一直是一个有争议的话题。在这里,我们表明,在S期早期,着丝粒与微管分离1-2分钟,并从纺锤体极移位。这些分离和移位事件是由着丝粒DNA复制引起的,这导致动粒解体。不久之后,动粒重新组装,导致它们被微管重新捕获。我们还展示了动粒随后如何被微管向极运输。我们的研究为封闭有丝分裂中S期的动粒-微管相互作用和动粒复制提供了新的见解。