有丝分裂
核孔蛋白
染色体分离
核孔
拉明
细胞生物学
生物
主轴装置
细胞分裂
主轴检查点
乙酰化
细胞周期
染色体
遗传学
细胞核
细胞
核运输
基因
细胞质
核心
作者
Hameed Akbar,Jun Cao,Dongmei Wang,Xiao Yuan,Manjuan Zhang,Saravanakumar Muthusamy,Xiaoyu Song,Xu Liu,Felix Aikhionbare,Xuebiao Yao,Xiaolan Gao,Xing Liu
摘要
ABSTRACT Stable transmission of genetic information during cell division requires faithful mitotic spindle assembly and chromosome segregation. In eukaryotic cells, nuclear envelope breakdown (NEBD) is required for proper chromosome segregation. Although a list of mitotic kinases has been implicated in NEBD, how they coordinate their activity to dissolve the nuclear envelope and protein machinery such as nuclear pore complexes was unclear. Here, we identified a regulatory mechanism in which Nup62 is acetylated by TIP60 in human cell division. Nup62 is a novel substrate of TIP60, and the acetylation of Lys432 by TIP60 dissolves nucleoporin Nup62–Nup58–Nup54 complex during entry into mitosis. Importantly, this acetylation-elicited remodeling of nucleoporin complex promotes the distribution of Nup62 to the mitotic spindle, which is indispensable for orchestrating correct spindle orientation. Moreover, suppression of Nup62 perturbs accurate chromosome segregation during mitosis. These results establish a previously uncharacterized regulatory mechanism in which TIP60-elicited nucleoporin dynamics promotes chromosome segregation in mitosis.
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