Kinesin-binding protein ensures accurate chromosome segregation by buffering KIF18A and KIF15

被引:23
|
作者
Malaby, Heidi L. H. [1 ]
Dumas, Megan E. [2 ]
Ohi, Ryoma [3 ,4 ]
Stumpff, Jason [1 ]
机构
[1] Univ Vermont, Dept Mol Physiol & Biophys, Burlington, VT 05405 USA
[2] Vanderbilt Univ, Dept Cell & Dev Biol, Med Sch, Nashville, TN USA
[3] Univ Michigan, Sch Med, Inst Life Sci, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
来源
JOURNAL OF CELL BIOLOGY | 2019年 / 218卷 / 04期
基金
美国国家卫生研究院;
关键词
MICROTUBULE DYNAMICS; INHIBITOR; MOVEMENTS; MECHANISM; DRIVEN; P21;
D O I
10.1083/jcb.201806195
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitotic kinesins must be regulated to ensure a precise balance of spindle forces and accurate segregation of chromosomes into daughter cells. Here, we demonstrate that kinesin-binding protein (KBP) reduces the activity of KIF18A and KIF15 during metaphase. Overexpression of KBP disrupts the movement and alignment of mitotic chromosomes and decreases spindle length, a combination of phenotypes observed in cells deficient for KIF18A and KIF15, respectively. We show through gliding filament and microtubule co-pelleting assays that KBP directly inhibits KIF18A and KIF15 motor activity by preventing microtubule binding. Consistent with these effects, the mitotic localizations of KIF18A and KIF15 are altered by overexpression of KBP. Cells depleted of KBP exhibit lagging chromosomes in anaphase, an effect that is recapitulated by KIF15 and KIF18A overexpression. Based on these data, we propose a model in which KBP acts as a protein buffer in mitosis, protecting cells from excessive KIF18A and KIF15 activity to promote accurate chromosome segregation.
引用
收藏
页码:1218 / 1234
页数:17
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