Cdk2 kinase is required for entry into mitosis as a positive regulator of Cdc2-cyclin B kinase activity

被引:201
作者
Guadagno, TM
Newport, JW
机构
[1] Department of Biology, University of California, San Diego, San Diego
关键词
D O I
10.1016/S0092-8674(00)80994-0
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 higher eukaryotes, Cdk2 kinase plays an essential role in regulating the G1-S transition. Here, we use cycling Xenopus egg extracts to examine the requirement of Cdk2 kinase on progression into mitosis. Interestingly, when Cdk2 kinase activity is inhibited by the Cdk-specific inhibitor, p21(Clp1), a block to mitosis occurs, and inactive Cdc2-cyclin B accumulates. This block occurs in the absence of nuclei and is not due to direct inhibition of Cdc2 by Cip. Importantly, this block to mitosis is reversible by restoring Cdk2-cyclin E kinase activity to a Cip-treated cycling extract. Moreover, immunodepletion of Cdk2 from interphase extracts prevents activation of Cdc2 upon the addition of exogenous cyclin B. Thus, our data show that Cdk2 kinase is a positive regulator of Cdc2-cyclin B complexes and establish a link between Cdk2 kinase and cell cycle progression into mitosis.
引用
收藏
页码:73 / 82
页数:10
相关论文
共 57 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 [J].
AMON, A ;
IRNIGER, S ;
NASMYTH, K .
CELL, 1994, 77 (07) :1037-1050
[2]   CELL-CYCLE REGULATION OF THE P34(CDC2) INHIBITORY KINASES [J].
ATHERTONFESSLER, S ;
LIU, F ;
GABRIELLI, B ;
LEE, MS ;
PENG, CY ;
PIWNICAWORMS, H .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (09) :989-1001
[3]   PHOSPHORYLATION INDEPENDENT ACTIVATION OF HUMAN CYCLIN-DEPENDENT KINASE-2 BY CYCLIN-A INVITRO [J].
CONNELLCROWLEY, L ;
SOLOMON, MJ ;
WEI, N ;
HARPER, JW .
MOLECULAR BIOLOGY OF THE CELL, 1993, 4 (01) :79-92
[4]   COMPLETION OF DNA-REPLICATION IS MONITORED BY A FEEDBACK-SYSTEM THAT CONTROLS THE INITIATION OF MITOSIS INVITRO - STUDIES IN XENOPUS [J].
DASSO, M ;
NEWPORT, JW .
CELL, 1990, 61 (05) :811-823
[5]   CDC2 PROTEIN-KINASE IS COMPLEXED WITH BOTH CYCLIN-A AND CYCLIN-B - EVIDENCE FOR PROTEOLYTIC INACTIVATION OF MPF [J].
DRAETTA, G ;
LUCA, F ;
WESTENDORF, J ;
BRIZUELA, L ;
RUDERMAN, J ;
BEACH, D .
CELL, 1989, 56 (05) :829-838
[6]   ASSOCIATION OF HUMAN CYCLIN-E WITH A PERIODIC G(1)-S PHASE PROTEIN-KINASE [J].
DULIC, V ;
LEES, E ;
REED, SI .
SCIENCE, 1992, 257 (5078) :1958-1961
[7]   THE CDC25 PROTEIN CONTAINS AN INTRINSIC PHOSPHATASE-ACTIVITY [J].
DUNPHY, WG ;
KUMAGAI, A .
CELL, 1991, 67 (01) :189-196
[8]   THE XENOPUS CDC2 PROTEIN IS A COMPONENT OF MPF, A CYTOPLASMIC REGULATOR OF MITOSIS [J].
DUNPHY, WG ;
BRIZUELA, L ;
BEACH, D ;
NEWPORT, J .
CELL, 1988, 54 (03) :423-431
[9]   FISSION YEAST GENES INVOLVED IN COUPLING MITOSIS TO COMPLETION OF DNA-REPLICATION [J].
ENOCH, T ;
CARR, AM ;
NURSE, P .
GENES & DEVELOPMENT, 1992, 6 (11) :2035-2046
[10]   EVIDENCE THAT THE G1-S AND G2-M TRANSITIONS ARE CONTROLLED BY DIFFERENT CDC2 PROTEINS IN HIGHER EUKARYOTES [J].
FANG, F ;
NEWPORT, JW .
CELL, 1991, 66 (04) :731-742