SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box

被引:1212
作者
Bai, C
Sen, P
Hofmann, K
Ma, L
Goebl, M
Harper, JW
Elledge, SJ
机构
[1] BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
[2] BAYLOR COLL MED,VERNA & MARRS MCLEAN DEPT BIOCHEM,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT MOL & HUMAN GENET,HOUSTON,TX 77030
[4] SWISS INST EXPTL CANC RES,BIOINFORMAT GRP,CH-1066 LAUSANNE,SWITZERLAND
[5] INDIANA UNIV,SCH MED,DEPT BIOCHEM & MOL BIOL,WALTHER ONCOL CTR,INDIANAPOLIS,IN 46202
关键词
D O I
10.1016/S0092-8674(00)80098-7
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
We have identified the yeast and human homologs of the SKP1 gene as a suppressor of cdc4 mutants and as a cyclin F-binding protein. Skp1p indirectly binds cyclin A/Cdk2 through Skp2p, and directly binds Skp2p, cyclin F, and Cdc4p through a novel structural motif called the F-box. SKP1 is required for ubiquitin-mediated proteolysis of Cln2p, Clb5p, and the Cdk inhibitor Sic1p, and provides a link between these molecules and the proteolysis machinery. A large number of proteins contain the F-box motif and are thereby implicated in the ubiquitin pathway. Different skp1 mutants arrest cells in either G1 or G2, suggesting a connection between regulation of proteolysis in different stages of the cycle.
引用
收藏
页码:263 / 274
页数:12
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