Association of human CUL-1 and ubiquitin-conjugating enzyme CDC34 with the F-box protein p45SKP2:: evidence for evolutionary conservation in the subunit composition of the CDC34-SCF pathway

被引:180
作者
Lisztwan, J [1 ]
Marti, A [1 ]
Sutterlüty, H [1 ]
Gstaiger, M [1 ]
Wirbelauer, C [1 ]
Krek, W [1 ]
机构
[1] Friedrich Miescher Inst, CH-4058 Basel, Switzerland
关键词
CDC34; cell cycle; cyclin-CDK; F-box; ubiquitination;
D O I
10.1093/emboj/17.2.368
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
In normal and transformed cells, the F-box protein p45(SKP2) is required for S phase and forms stable complexes with p19(SKP1) and cyclin A-cyclin-dependent kinase (CDK)2, Here we identify human CUL-1, a member of the cullin family, and the ubiquitin-conjugating enzyme CDC34 as additional partners of p45(SKP2) in vivo, CUL-1 also associates with cyclin A and p19(SKP1) in vivo and, with p45(SKP2), they assemble into a large multiprotein complex, In Saccharomyces cerevisiae, a complex of similar molecular composition (an F-box protein, a member of the cullin family and a homolog of p19(SKP1)) forms a functional E3 ubiquitin protein ligase complex, designated SCFCDC4, that facilitates ubiquitination of a CDK inhibitor by CDC34, The data presented here imply that the p45(SKP2)-CUL-1-p19(SKP1) complex may be a human representative of an SCF-type E3 ubiquitin protein ligase. We propose that all eukaryotic cells may use a common ubiquitin conjugation apparatus to promote S phase, Finally, we show that multiprotein complex formation involving p45(SKP2)-CUL-1 and p19(SKP1) is governed, in part, by periodic, S phase-specific accumulation of the p45(SKP2) subunit and by the p45(SKP2)-bound cyclin A-CDK2, The dependency of p45(SKP)-p19(SKP1) complex formation on cyclin A-CDK2 may ensure tight coordination of the activities of the cell cycle clock with those of a potential ubiquitin conjugation pathway.
引用
收藏
页码:368 / 383
页数:16
相关论文
共 78 条
[1]  
Adams PD, 1996, MOL CELL BIOL, V16, P6623
[2]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[3]   SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box [J].
Bai, C ;
Sen, P ;
Hofmann, K ;
Ma, L ;
Goebl, M ;
Harper, JW ;
Elledge, SJ .
CELL, 1996, 86 (02) :263-274
[4]   G(1) CYCLIN TURNOVER AND NUTRIENT-UPTAKE ARE CONTROLLED BY A COMMON PATHWAY IN YEAST [J].
BARRAL, Y ;
JENTSCH, S ;
MANN, C .
GENES & DEVELOPMENT, 1995, 9 (04) :399-409
[5]   The proteolysis of mitotic cyclins in mammalian cells persists from the end of mitosis until the onset of S phase [J].
Brandeis, M ;
Hunt, T .
EMBO JOURNAL, 1996, 15 (19) :5280-5289
[6]   Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein [J].
Campanero, MR ;
Flemington, EK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2221-2226
[7]   REVERSAL OF TERMINAL DIFFERENTIATION AND CONTROL OF DNA-REPLICATION - CYCLIN-A AND CDK2 SPECIFICALLY LOCALIZE AT SUBNUCLEAR SITES OF DNA-REPLICATION [J].
CARDOSO, MC ;
LEONHARDT, H ;
NADALGINARD, B .
CELL, 1993, 74 (06) :979-992
[8]   THE UBIQUITIN-PROTEASOME PROTEOLYTIC PATHWAY [J].
CIECHANOVER, A .
CELL, 1994, 79 (01) :13-21
[9]   Turnover of cyclin E by the ubiquitin-proteasome pathway is regulated by cdk2 binding and cyclin phosphorylation [J].
Clurman, BE ;
Sheaff, RJ ;
Thress, K ;
Groudine, M ;
Roberts, JM .
GENES & DEVELOPMENT, 1996, 10 (16) :1979-1990
[10]   ACTIVATION OF HUMAN CYCLIN-DEPENDENT KINASES INVITRO [J].
DESAI, D ;
GU, Y ;
MORGAN, DO .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (05) :571-582