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

被引:1200
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
相关论文
共 38 条
  • [1] CLOSING THE CELL-CYCLE CIRCLE IN YEAST - G2 CYCLIN PROTEOLYSIS INITIATED AT MITOSIS PERSISTS UNTIL THE ACTIVATION OF G1 CYCLINS IN THE NEXT CYCLE
    AMON, A
    IRNIGER, S
    NASMYTH, K
    [J]. CELL, 1994, 77 (07) : 1037 - 1050
  • [2] HUMAN CYCLIN-F
    BAI, C
    RICHMAN, R
    ELLEDGE, SJ
    [J]. EMBO JOURNAL, 1994, 13 (24) : 6087 - 6098
  • [3] BANERJEE A, 1993, J BIOL CHEM, V270, P26209
  • [4] G(1) CYCLIN TURNOVER AND NUTRIENT-UPTAKE ARE CONTROLLED BY A COMMON PATHWAY IN YEAST
    BARRAL, Y
    JENTSCH, S
    MANN, C
    [J]. GENES & DEVELOPMENT, 1995, 9 (04) : 399 - 409
  • [5] A flexible motif search technique based on generalized profiles
    Bucher, P
    Karplus, K
    Moeri, N
    Hofmann, K
    [J]. COMPUTERS & CHEMISTRY, 1996, 20 (01): : 3 - 23
  • [6] 2 DNA-BINDING FACTORS RECOGNIZE SPECIFIC SEQUENCES AT SILENCERS, UPSTREAM ACTIVATING SEQUENCES, AUTONOMOUSLY REPLICATING SEQUENCES, AND TELOMERES IN SACCHAROMYCES-CEREVISIAE
    BUCHMAN, AR
    KIMMERLY, WJ
    RINE, J
    KORNBERG, RD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) : 210 - 225
  • [7] CONNELLY C, 1996, IN PRESS CELL, V86
  • [9] UBIQUITINATION OF THE G(1) CYCLIN CLN2P BY A CDC34P-DEPENDENT PATHWAY
    DESHAIES, RJ
    CHAU, V
    KIRSCHNER, M
    [J]. EMBO JOURNAL, 1995, 14 (02) : 303 - 312
  • [10] P40(SDB25), A PUTATIVE CDK INHIBITOR, HAS A ROLE IN THE M/G(1) TRANSITION IN SACCHAROMYCES-CEREVISIAE
    DONOVAN, JD
    TOYN, JH
    JOHNSON, AL
    JOHNSTON, LH
    [J]. GENES & DEVELOPMENT, 1994, 8 (14) : 1640 - 1653