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A mitotic septin scaffold required for mammalian chromosome congression and segregation
被引:201
作者:
Spiliotis, ET
Kinoshita, M
Nelson, WJ
[1
]
机构:
[1] Stanford Univ, Sch Med, Beckman Ctr Mol & Genet Med, Dept Cellular & Mol Physiol, Stanford, CA 94305 USA
[2] Kyoto Univ, Grad Sch Med, Biochem & Cell Biol Unit, Horizontal Med Res Org, Kyoto 6068501, Japan
来源:
关键词:
D O I:
10.1126/science.1106823
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:
07 ;
0710 ;
09 ;
摘要:
Coordination of cytokinesis with chromosome congression and segregation is critical for proper cell division, but the mechanism is unknown. Here, septins, a conserved family of polymerizing guanosine triphosphate-binding proteins, localized to the metaphase plate during mitosis. Septin depletion resulted in chromosome loss from the metaphase plate, lack of chromosome segregation and spindle elongation, and incomplete cytokinesis upon delayed mitotic exit. These defects correlated with loss of the mitotic motor and the checkpoint regulator centromere-associated protein E (CENP-E) from the kinetochores of congressing chromosomes. Mammalian septins may thus form a mitotic scaffold for CENP-E and other effectors to coordinate cytokinesis with chromosome congression and segregation.
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页码:1781 / 1785
页数:5
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