The Rab6-binding kinesin, Rab6-KIFL, is required for cytokinesis

被引:174
作者
Hill, E
Clarke, N
Barr, FA
机构
[1] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Biol & Life Sci, CRC, Beatson Labs, Glasgow G61 1BD, Lanark, Scotland
[3] Max Planck Inst Biochem, Dept Cell Biol, D-82152 Martinsried, Germany
关键词
cytokinesis; Golgi; kinesin; mitosis; Rab;
D O I
10.1093/emboj/19.21.5711
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Rab6-binding kinesin, Rab6-KIFL, was identified in a two-hybrid screen for proteins that interact with Rab6, a small GTPase involved in membrane traffic through the Golgi apparatus, We find that Rab6-KIFL accumulates in mitotic cells where it localizes to the midzone of the spindle during anaphase, and to the cleavage furrow and midbody during telophase. Overexpression of Rab6-KIFL causes a cell division defect resulting in cell death. Microinjection of antibodies to Rab6-KTFL results in the cells becoming binucleate after one cell cycle, and time-lapse microscopy reveals that this is due to a defect in cleavage furrow formation and thus cytokinesis. These data show that endogenous Rab6-KIFL functions in cell division during cleavage furrow formation and cytokinesis, in addition to its previously described role in membrane traffic.
引用
收藏
页码:5711 / 5719
页数:9
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