The molecular basis for the regulation of the cap-binding complex by the importins

被引:74
作者
Dias, Sandra M. G. [1 ]
Wilson, Kristin F. [1 ]
Rojas, Katherine S. [1 ]
Ambrosio, Andre L. B. [1 ]
Cerione, Richard A. [1 ,2 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Mol Med, Ithaca, NY 14853 USA
[2] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY USA
基金
美国国家卫生研究院;
关键词
SMALL-ANGLE SCATTERING; NUCLEAR-LOCALIZATION SIGNAL; U-SNRNA EXPORT; X-RAY SOLUTION; MESSENGER-RNA; STRUCTURAL BASIS; PROTEIN COMPLEX; BIOLOGICAL MACROMOLECULES; CRYSTALLOGRAPHIC ANALYSIS; KARYOPHERIN ALPHA;
D O I
10.1038/nsmb.1649
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 binding of capped RNAs to the cap-binding complex (CBC) in the nucleus, and their dissociation from the CBC in the cytosol, represent essential steps in RNA processing. Here we show how the nucleocytoplasmic transport proteins importin-alpha and importin-beta have key roles in regulating these events. As a first step toward understanding the molecular basis for this regulation, we determined a 2.2-angstrom resolution X-ray structure for a CBC-importin-alpha complex that provides a detailed picture for how importin-alpha binds to the CBP80 subunit of the CBC. Through a combination of biochemical studies, X-ray crystallographic information and small-angle scattering experiments, we then determined how importin-beta binds to the CBC through its CBP20 subunit. Together, these studies enable us to propose a model describing how importin-beta stimulates the dissociation of capped RNA from the CBC in the cytosol following its nuclear export.
引用
收藏
页码:930 / U51
页数:10
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