Modeling the fission yeast cell cycle:: Quantized cycle times in wee1- cdc25Δ mutant cells

被引:88
作者
Sveiczer, A
Csikasz-Nagy, A
Gyorffy, B
Tyson, JJ
Novak, B
机构
[1] Budapest Univ Technol & Econ, Dept Agr Chem Technol, H-1521 Budapest, Hungary
[2] Virginia Polytech Inst & State Univ, Dept Biol, Blacksburg, VA 24061 USA
关键词
D O I
10.1073/pnas.97.14.7865
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A detailed mathematical model for the fission yeast mitotic cycle is developed based on positive and negative feedback loops by which Cdc13/Cdc2 kinase activates and inactivates itself. Positive feedbacks are created by Cdc13/Cdc2-dependent phosphorylation of specific substrates: inactivating its negative regulators (Rum1, Ste9 and Wee1/Mik1) and activating its positive regulator (Cdc25). A slow negative feedback loop is turned on during mitosis by activation of Slp1/anaphase-promoting complex (APC), which indirectly re-activates the negative regulators, leading to a drop in Cdc13/Cdc2 activity and exit from mitosis. The model explains how fission yeast cells can exit mitosis in the absence of Ste9 (Cdc13 degradation) and Rum1 (an inhibitor of Cdc13/Cdc2). We also show that, if the positive feedback loops accelerating the G(2)/M transition (through Wee1 and Cdc25) are weak, then cells can reset back to G(2) from early stages of mitosis by premature activation of the negative feedback loop. This resetting can happen more than once, resulting in a quantized distribution of cycle times, as observed experimentally in wee1(-) cdc25 Delta mutant cells. Our quantitative description of these quantized cycles demonstrates the utility of mathematical modeling, because these cycles cannot be understood by intuitive arguments alone.
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页码:7865 / 7870
页数:6
相关论文
共 42 条
[1]   Regulation of Schizosaccharomyces pombe Wee1 tyrosine kinase [J].
Aligue, R ;
Wu, L ;
Russell, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) :13320-13325
[2]   Regulation of the G1 phase of the cell cycle by periodic stabilization and degradation of the p25rum1 CDK inhibitor [J].
Benito, J ;
Martín-Castellanos, C ;
Moreno, S .
EMBO JOURNAL, 1998, 17 (02) :482-497
[3]   P25(RUM1) ORDERS S-PHASE AND MITOSIS BY ACTING AS AN INHIBITOR OF THE P34(CDC2) MITOTIC KINASE [J].
CORREABORDES, J ;
NURSE, P .
CELL, 1995, 83 (06) :1001-1009
[4]  
CREANOR J, 1994, J CELL SCI, V107, P1197
[5]  
ENOCH T, 1991, COLD SH Q B, V56, P409
[6]   EPISTATIC GENE INTERACTIONS IN THE CONTROL OF DIVISION IN FISSION YEAST [J].
FANTES, P .
NATURE, 1979, 279 (5712) :428-430
[7]   CYCLINS OF THE FISSION YEAST SCHIZOSACCHAROMYCES-POMBE [J].
FISHER, D ;
NURSE, P .
SEMINARS IN CELL BIOLOGY, 1995, 6 (02) :73-78
[8]   A single fission yeast mitotic cyclin B p34(cdc2) kinase promotes both S-phase and mitosis in the absence of G(1) cyclins [J].
Fisher, DL ;
Nurse, P .
EMBO JOURNAL, 1996, 15 (04) :850-860
[9]   A MINIMAL CASCADE MODEL FOR THE MITOTIC OSCILLATOR INVOLVING CYCLIN AND CDC2 KINASE [J].
GOLDBETER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :9107-9111
[10]   AN AMPLIFIED SENSITIVITY ARISING FROM COVALENT MODIFICATION IN BIOLOGICAL-SYSTEMS [J].
GOLDBETER, A ;
KOSHLAND, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (11) :6840-6844