Spindle assembly checkpoint proteins are positioned close to core microtubule attachment sites at kinetochores

被引:50
|
作者
Varma, Dileep [1 ]
Wan, Xiaohu [1 ]
Cheerambathur, Dhanya [2 ,3 ]
Gassmann, Reto [2 ,3 ]
Suzuki, Aussie [1 ]
Lawrimore, Josh [1 ]
Desai, Arshad [2 ,3 ]
Salmon, E. D. [1 ]
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Univ Calif San Diego, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
来源
JOURNAL OF CELL BIOLOGY | 2013年 / 202卷 / 05期
基金
美国国家卫生研究院;
关键词
MITOTIC CHECKPOINT; DYNEIN; COMPLEX; HEC1; DYNAMICS; ZWINT-1; BINDING; MAD1; NUF2; ZW10;
D O I
10.1083/jcb.201304197
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Spindle assembly checkpoint proteins have been thought to reside in the peripheral corona region of the kinetochore, distal to microtubule attachment sites at the outer plate. However, recent biochemical evidence indicates that checkpoint proteins are closely linked to the core kinetochore microtubule attachment site comprised of the Knl1-Misl2-Ndc80 (KMN) complexes/KMN network. In this paper, we show that the Knl1-Zwint1 complex is required to recruit the Rod-Zwilch-Zw10 (RZZ) and Mad1-Mad2 complexes to the outer kinetochore. Consistent with this, nanometer-scale mapping indicates that RZZ, Mad1-Mad2, and the C terminus of the dynein recruitment factor Spindly are closely juxtaposed with the KMN network in metaphase cells when their dissociation is blocked and the checkpoint is active. In contrast, the N terminus of Spindly is similar to 75 nm outside the calponin homology domain of the Ndc80 complex. These results reveal how checkpoint proteins are integrated within the substructure of the kinetochore and will aid in understanding the coordination of microtubule attachment and checkpoint signaling during chromosome segregation.
引用
收藏
页码:735 / 746
页数:12
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