Npap60/Nup50 is a tri-stable switch that stimulates importin-α:β-mediated nuclear protein import

被引:100
作者
Lindsay, ME
Plafker, K
Smith, AE
Clurman, BE
Macara, IG [1 ]
机构
[1] Univ Virginia, Sch Med, Ctr Cell Signaling, Charlottesville, VA 22908 USA
[2] Univ Virginia, Sch Med, Dept Microbiol, Charlottesville, VA 22908 USA
[3] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
关键词
D O I
10.1016/S0092-8674(02)00836-X
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
Many nuclear-targeted proteins are transported through the nuclear pore complex (NPC) by the importin-alpha:beta receptor. We now show that Npap60 (also called Nup50), a protein previously believed to be a structural component of the NPC, is a Ran binding protein and a cofactor for importin-alpha:beta-mediated import. Npap60 is a tri-stable switch that alternates between binding modes. The C terminus binds importin-P through RanGTP. The N terminus binds the C terminus of importin-alpha, while a central domain binds importin-beta. Npap60:importin-alpha:beta binds cargo and can stimulate nuclear import. Endogenous Npap60 can shuttle and is accessible from the cytoplasmic side of the nuclear envelope. These results identify Npap60 as a cofactor for importin-alpha:beta nuclear import and as a previously unidentified subunit of the importin complex.
引用
收藏
页码:349 / 360
页数:12
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