Crosstalk Between Microtubule Attachment Complexes Ensures Accurate Chromosome Segregation

被引:82
作者
Cheerambathur, Dhanya K. [1 ]
Gassmann, Reto [1 ]
Cook, Brian [1 ]
Oegema, Karen [1 ]
Desai, Arshad [1 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
关键词
KINETOCHORE; SPINDLE; CHECKPOINT; DYNEIN; INTERFACE; MECHANISM; PROTEIN;
D O I
10.1126/science.1246232
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The microtubule-based mitotic spindle segregates chromosomes during cell division. During chromosome segregation, the centromeric regions of chromosomes build kinetochores that establish end-coupled attachments to spindle microtubules. Here, we used the Caenorhabditis elegans embryo as a model system to examine the crosstalk between two kinetochore protein complexes implicated in temporally distinct stages of attachment formation. The kinetochore dynein module, which mediates initial lateral microtubule capture, inhibited microtubule binding by the Ndc80 complex, which ultimately forms the end-coupled attachments that segregate chromosomes. The kinetochore dynein module directly regulated Ndc80, independently of phosphorylation by Aurora B kinase, and this regulation was required for accurate segregation. Thus, the conversion from initial dynein-mediated, lateral attachments to correctly oriented, Ndc80-mediated end-coupled attachments is actively controlled.
引用
收藏
页码:1239 / 1242
页数:4
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