Small GTPase Rab5 participates in chromosome congression and regulates localization of the centromere- associated protein CENP-F to kinetochores

被引:42
|
作者
Serio, Gaetana [1 ]
Margaria, Valentina [1 ,2 ]
Jensen, Sanne [3 ]
Oldani, Amanda [4 ]
Bartek, Jiri [2 ,3 ,5 ]
Bussolino, Federico [1 ]
Lanzetti, Letizia [1 ]
机构
[1] Univ Turin, Dipartimento Sci Oncol, Ist Ric & Cura Canc, I-10060 Turin, Italy
[2] Danish Canc Soc, Inst Canc Biol, DK-2100 Copenhagen, Denmark
[3] Danish Canc Soc, Ctr Genotox Stress Res, DK-2100 Copenhagen, Denmark
[4] Fdn Italiana Ric Canc, IFOM Ist, I-20139 Milan, Italy
[5] Palacky Univ, Inst Mol & Translat Med, CZ-77515 Olomouc, Czech Republic
基金
新加坡国家研究基金会;
关键词
endocytosis; mitosis; EARLY ENDOCYTIC PATHWAY; MITOTIC CHECKPOINT; SPINDLE; RECEPTOR; TRAFFICKING; ATTACHMENT; NETWORK; MITOSIS; MATRIX; RAC;
D O I
10.1073/pnas.1103516108
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
Rab5 is a small GTPase known to regulate vesicular trafficking during interphase. Here, we show that Rab5 also plays an unexpected role during mitotic progression. RNAi-mediated silencing of Rab5 caused defects in chromosome congression and extensive prometaphase delay, and it correlated with a severe reduction in the localization of the centromere-associated protein CENP-F to kinetochores. CENP-F is a component of the nuclear matrix required for chromosome congression that, at mitotic entry, localizes to the nuclear envelope and assembles on kinetochores, contributing to the establishment of kinetochore microtubule interactions. We found that Rab5 forms a complex with a subset of CENP-F in mitotic cells and regulates the kinetics of release of CENP-F from the nuclear envelope and its accumulation on kinetochores. Simultaneous depletion of both Rab5 and CENP-F recapitulated the mitotic defects caused by silencing of either Rab5 or CENP-F alone, indicating epistatic roles for these two proteins in the pathway that orchestrates chromosome congression. These results reveal the involvement of Rab5 in the proper execution of mitotic programs whose deregulation can undermine chromosomal stability.
引用
收藏
页码:17337 / 17342
页数:6
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