Multi-rhythmicity generated by coupling two cellular rhythms

被引:25
作者
Yan, Jie [1 ,2 ]
Goldbeter, Albert [2 ]
机构
[1] Soochow Univ, Sch Math Sci, Ctr Syst Biol, Suzhou, Peoples R China
[2] ULB, Fac Sci, Unite Chronobiol Theor, Brussels, Belgium
基金
中国国家自然科学基金;
关键词
oscillations; biological rhythms; multiple attractors; birhythmicity; trirhythmicity; FINAL-STATE SENSITIVITY; CIRCADIAN OSCILLATIONS; MODEL; BIRHYTHMICITY; BISTABILITY; CLOCK; CHAOS; MULTISTABILITY; TRANSITIONS; SUPPRESSION;
D O I
10.1098/rsif.2018.0835
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
The cell cycle and the circadian clock represent two major cellular rhythms, which are coupled because the circadian clock governs the synthesis of several proteins of the network that drives the mammalian cell cycle. Analysis of a detailed model for these coupled cellular rhythms previously showed that the cell cycle can be entrained at the circadian period of 24 h, or at a period of 48 h, depending on the autonomous period of the cell cycle and on the coupling strength. We show by means of numerical simulations that multiple stable periodic regimes, i.e. multi-rhythmicity, may originate from the coupling of the two cellular rhythms. In these conditions, the cell cycle can evolve to any one of two (birhythmicity) or three stable periodic regimes (trirhythmicity). When applied at the right phase, transient perturbations of appropriate duration and magnitude can induce the switch between the different oscillatory states. Such switching is characterized by final state sensitivity, which originates from the complex structure of the attraction basins. By providing a novel instance of multi-rhythmicity in a realistic model for the coupling of two major cellular rhythms, the results throw light on the conditions in which multiple stable periodic regimes may coexist in biological systems.
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页数:12
相关论文
共 58 条
[1]   A Theoretical Exploration of Birhythmicity in the p53-Mdm2 Network [J].
Abou-Jaoude, Wassim ;
Chaves, Madalena ;
Gouze, Jean-Luc .
PLOS ONE, 2011, 6 (02)
[2]   SYSTEMATIC DESIGN OF CHEMICAL OSCILLATORS .16. BIRHYTHMICITY AND COMPOUND OSCILLATION IN COUPLED CHEMICAL OSCILLATORS - CHLORITE-BROMATE-IODIDE SYSTEM [J].
ALAMGIR, M ;
EPSTEIN, IR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (08) :2500-2502
[3]   Phase transitions in physiologic coupling [J].
Bartsch, Ronny P. ;
Schumann, Aicko Y. ;
Kantelhardt, Jan W. ;
Penzel, Thomas ;
Ivanov, Plamen Ch .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (26) :10181-10186
[4]  
Bernard C., 1878, Lecons sur les phenomenes de la vie communs aux animaux et aux vegetaux
[5]   Robust synchronization of coupled circadian and cell cycle oscillators in single mammalian cells [J].
Bieler, Jonathan ;
Cannavo, Rosamaria ;
Gustafson, Kyle ;
Gobet, Cedric ;
Gatfield, David ;
Naef, Felix .
MOLECULAR SYSTEMS BIOLOGY, 2014, 10 (07)
[6]   Control of birhythmicity: A self-feedback approach [J].
Biswas, Debabrata ;
Banerjee, Tanmoy ;
Kurths, Juergen .
CHAOS, 2017, 27 (06)
[7]  
Cannon W.B., 1932, The Wisdom of the Body
[8]   Cell Fate Specification Based on Tristability in the Inner Cell Mass of Mouse Blastocysts [J].
De Mot, Laurane ;
Gonze, Didier ;
Bessonnard, Sylvain ;
Chazaud, Claire ;
Goldbeter, Albert ;
Dupont, Genevieve .
BIOPHYSICAL JOURNAL, 2016, 110 (03) :710-722
[9]   MULTIPLE PERIODIC REGIMES AND FINAL-STATE SENSITIVITY IN A BIOCHEMICAL SYSTEM [J].
DECROLY, O ;
GOLDBETER, A .
PHYSICS LETTERS A, 1984, 105 (4-5) :259-262
[10]   FROM SIMPLE TO COMPLEX OSCILLATORY BEHAVIOR - ANALYSIS OF BURSTING IN A MULTIPLY REGULATED BIOCHEMICAL SYSTEM [J].
DECROLY, O ;
GOLDBETER, A .
JOURNAL OF THEORETICAL BIOLOGY, 1987, 124 (02) :219-250