COMPLETION OF DNA-REPLICATION IS MONITORED BY A FEEDBACK-SYSTEM THAT CONTROLS THE INITIATION OF MITOSIS INVITRO - STUDIES IN XENOPUS

被引:326
作者
DASSO, M
NEWPORT, JW
机构
[1] Department of Biology University of California at San Diego, La Jolla
关键词
D O I
10.1016/0092-8674(90)90191-G
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
During cell division complete DNA replication must occur before mitosis is initiated. Using a cell-free extract derived from Xenopus eggs that oscillates between S phase and mitosis, we have investigated how completion of DNA synthesis is coupled to the initiation of mitosis. We find that Xenopus eggs contain a feedback pathway which suppresses mitosis until replication is completed and that activation of this inhibitory system is dependent on the presence of a threshold concentration of unreplicated DNA. We demonstrate that in the presence of unreplicated DNA the active feedback system inhibits initiation of mitosis by blocking the activation of MPF, a regulator of mitosis found in all eukaryotic cells. Our results demonstrate that the feedback system does not inhibit MPF activation by blocking the synthesis or accumulation of cyclin protein, a subunit of MPF, or by blocking association of cyclin with the cdc2 subunit of MPF. We propose that the feedback system blocks mitosis by maintaining MPF in an inactive state by modulating posttranslational modifications critical for MPF activation. © 1990.
引用
收藏
页码:811 / 823
页数:13
相关论文
共 51 条
[1]  
ANDERSON CW, 1973, J VIROL, V106, P1445
[2]   CDC2 IS A COMPONENT OF THE M-PHASE SPECIFIC HISTONE-H1 KINASE - EVIDENCE FOR IDENTITY WITH MPF [J].
ARION, D ;
MEIJER, L ;
BRIZUELA, L ;
BEACH, D .
CELL, 1988, 55 (02) :371-378
[3]   ACTIVATION OF HUMAN CDC2 PROTEIN AS A HISTONE H-1 KINASE IS ASSOCIATED WITH COMPLEX-FORMATION WITH THE P62 SUBUNIT [J].
BRIZUELA, L ;
DRAETTA, G ;
BEACH, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4362-4366
[4]   HUMAN CDC2 PROTEIN-KINASE IS A MAJOR CELL-CYCLE REGULATED TYROSINE KINASE SUBSTRATE [J].
DRAETTA, G ;
PIWNICAWORMS, H ;
MORRISON, D ;
DRUKER, B ;
ROBERTS, T ;
BEACH, D .
NATURE, 1988, 336 (6201) :738-744
[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]   UNRAVELING OF MITOTIC CONTROL MECHANISMS [J].
DUNPHY, WG ;
NEWPORT, JW .
CELL, 1988, 55 (06) :925-928
[7]   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
[8]   FISSION YEAST P13 BLOCKS MITOTIC ACTIVATION AND TYROSINE DEPHOSPHORYLATION OF THE XENOPUS CDC2 PROTEIN-KINASE [J].
DUNPHY, WG ;
NEWPORT, JW .
CELL, 1989, 58 (01) :181-191
[9]   MITOSIS-INDUCING FACTORS ARE PRESENT IN A LATENT FORM DURING INTERPHASE IN THE XENOPUS EMBRYO [J].
DUNPHY, WG ;
NEWPORT, JW .
JOURNAL OF CELL BIOLOGY, 1988, 106 (06) :2047-2056
[10]   CYCLIN - A PROTEIN SPECIFIED BY MATERNAL MESSENGER-RNA IN SEA-URCHIN EGGS THAT IS DESTROYED AT EACH CLEAVAGE DIVISION [J].
EVANS, T ;
ROSENTHAL, ET ;
YOUNGBLOM, J ;
DISTEL, D ;
HUNT, T .
CELL, 1983, 33 (02) :389-396