Cell cycle regulated transport controlled by alterations in the nuclear pore complex

被引:125
作者
Makhnevych, T
Lusk, CP
Anderson, AM
Aitchison, JD [1 ]
Wozniak, RW
机构
[1] Univ Alberta, Dept Cell Biol, Edmonton, AB T6G 2H7, Canada
[2] Inst Syst Biol, Seattle, WA 98103 USA
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0092-8674(03)00986-3
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
Eukaryotic cells have developed mechanisms for regulating the nuclear transport of macromolecules that control various cellular events including movement through defined stages of the cell cycle. In yeast cells, where the nuclear envelope remains intact throughout the cell cycle, these transport regulatory mechanisms must also function during mitosis. We have uncovered a mechanism for regulating transport that is controlled by M phase specific molecular rearrangements in the nuclear pore complex (NPC). These changes allow a transport inhibitory nucleoporin, Nup53p, to bind the karyopherin Kap121p specifically during mitosis, slowing its movement through the NPC and inducing cargo release. Yeast strains that possess defects in the function of Kap121p or the fidelity of the inhibitory pathway are delayed in mitosis. We propose that fluctuations in Kap121p transport mediated by the NPC contribute to controlling the subcellular distribution of molecules that direct progression through mitosis.
引用
收藏
页码:813 / 823
页数:11
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