Elevated polar ejection forces stabilize kinetochore-microtubule attachments

被引:61
作者
Cane, Stuart [1 ,2 ]
Ye, Anna A. [1 ,2 ]
Luks-Morgan, Sasha J. [1 ]
Maresca, Thomas J. [1 ,2 ]
机构
[1] Univ Massachusetts, Dept Biol, Amherst, MA 01003 USA
[2] Univ Massachusetts, Mol & Cellular Biol Grad Program, Amherst, MA 01003 USA
基金
美国国家科学基金会;
关键词
KINESIN-LIKE PROTEIN; METAPHASE CHROMOSOME ALIGNMENT; SPINDLE ASSEMBLY CHECKPOINT; HISTONE H3 PHOSPHORYLATION; MITOTIC SPINDLE; AURORA-B; CHROMOKINESIN KID; IN-VITRO; DIRECTIONAL INSTABILITY; DROSOPHILA-MELANOGASTER;
D O I
10.1083/jcb.201211119
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Chromosome biorientation promotes congression and generates tension that stabilizes kinetochore-microtubule (kt-MT) interactions. Forces produced by molecular motors also contribute to chromosome alignment, but their impact on kt-MT attachment stability is unclear. A critical force that acts on chromosomes is the kinesin-10-dependent polar ejection force (PEF). PEFs are proposed to facilitate congression by pushing chromosomes away from spindle poles, although knowledge of the molecular mechanisms underpinning PEF generation is incomplete. Here, we describe a live-cell PEF assay in which tension was applied to chromosomes by manipulating levels of the chromokinesin NOD (no distributive disjunction; Drosophila melanogaster kinesin-10). NOD stabilized syntelic kt-MT attachments in a dose-and motor-dependent manner by overwhelming the ability of Aurora B to mediate error correction. NOD-coated chromatin stretched away from the pole via lateral and end-on interactions with microtubules, and NOD chimeras with either plus end-directed motility or tip-tracking activity produced PEFs. Thus, kt-MT attachment stability is modulated by PEFs, which can be generated by distinct force-producing interactions between chromosomes and dynamic spindle microtubules.
引用
收藏
页码:203 / 218
页数:16
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