Molecular Biomedical Sciences Department, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607.
Quantitative and Computational Developmental Biology Cluster, North Carolina State University, Raleigh, NC 27607.
Mol Biol Cell. 2023 Jul 1;34(8):ar77. doi: 10.1091/mbc.E23-01-0034. Epub 2023 Apr 26.
Cells actively position their nuclei based on their activity. In fission yeast, microtubule-dependent nuclear centering is critical for symmetrical cell division. After spindle disassembly at the end of anaphase, the nucleus recenters over an ∼90-min period, approximately half of the duration of the cell cycle. Live-cell and simulation experiments support the cooperation of two distinct microtubule competition mechanisms in the slow recentering of the nucleus. First, a push-push mechanism acts from spindle disassembly to septation and involves the opposing actions of the mitotic spindle pole body microtubules that push the nucleus away from the ends of the cell, while a postanaphase array of microtubules baskets the nucleus and limits its migration toward the division plane. Second, a slow-and-grow mechanism slowly centers the nucleus in the newborn cell by a combination of microtubule competition and asymmetric cell growth. Our work underlines how intrinsic properties of microtubules differently impact nuclear positioning according to microtubule network organization and cell size.
细胞根据其活性积极定位其细胞核。在裂殖酵母中,微管依赖性核定位对于对称细胞分裂至关重要。在后期纺锤体解体后,细胞核在大约 90 分钟的时间内重新定位,大约是细胞周期持续时间的一半。活细胞和模拟实验支持两种不同的微管竞争机制在核的缓慢重新定位中的合作。首先,一种推-推机制从纺锤体解体到隔膜形成发挥作用,涉及有丝分裂纺锤体极体微管的相反作用,它们将核推开远离细胞的两端,而后期微管的数组则将核包围起来并限制其向分裂面的迁移。其次,一个缓慢生长的机制通过微管竞争和不对称细胞生长的结合,将核缓慢地定位于新生细胞的中心。我们的工作强调了微管的固有特性如何根据微管网络组织和细胞大小的不同,对核定位产生不同的影响。