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Kunihiko Kaneko

Publications and source records attributed to Kunihiko Kaneko.

At least 73 records · Page 4Linked to original sources

Kinetic Selection of Template Polymer with Complex Sequences

Emergence and maintenance of polymers with complex sequences is a major question in the study of origins of life. To answer this, we studied a model polymerization reaction, where polymers are synthesized by stepwise ligation from two types of monomers, catalyzed by a long polymer as a template. Direct stochastic simulation and dynamical systems analysis revealed that the most dominant polymer sequence in a population successively changes against the flow rate of monomer to the system. The slower the flow, the more is the complex sequence selected. We discuss the relevance of this kinetic selection of sequence by the non-equilibrium flow rate to the origin of complex polymers.

physics.bio-ph↗

Collective $1/f$ fluctuation by pseudo-Casimir-invariants

In this study, we propose a universal scenario explaining the $1/f$ fluctuation, including pink noises, in Hamiltonian dynamical systems with many degrees of freedom under long-range interaction. In the thermodynamic limit, the dynamics of such systems can be described by the Vlasov equation, which has an infinite number of Casimir invariants. In a finite system, they become pseudoinvariants, which yield quasistationary states. The dynamics then exhibit slow motion over them, up to the timescale where the pseudo-Casimir-invariants are effective. Such long-time correlation leads to $1/f$ fluctuations of collective variables, as is confirmed by direct numerical simulations. The universality of this collective $1/f$ fluctuation is demonstrated by taking a variety of Hamiltonians and changing the range of interaction and number of particles.

nlin.CD↗

Cooperative reliable response from sloppy gene-expression dynamics

Gene expression dynamics satisfying given input-output relationships were investigated by evolving the networks for an optimal response. We found three types of networks and corresponding dynamics, depending on the sensitivity of gene expression dynamics: direct response with straight paths, amplified response by a feed-forward network, and cooperative response with a complex network. When the sensitivity of each gene's response is low and expression dynamics is sloppy, the last type is selected, in which many genes respond collectively to inputs, with local-excitation and global-inhibition structures. The result provides an insight into how a reliable response is achieved with unreliable units, and on why complex networks with many genes are adopted in cells.

q-bio.MN↗

Exponential growth for self-reproduction in a catalytic reaction network: relevance of a minority molecular species and crowdedness

Explanation of exponential growth in self-reproduction is an important step toward elucidation of the origins of life because optimization of the growth potential across rounds of selection is necessary for Darwinian evolution. To produce another copy with approximately the same composition, the exponential growth rates for all components have to be equal. How such balanced growth is achieved, however, is not a trivial question, because this kind of growth requires orchestrated replication of the components in stochastic and nonlinear catalytic reactions. By considering a mutually catalyzing reaction in two- and three-dimensional lattices, as represented by a cellular automaton model, we show that self-reproduction with exponential growth is possible only when the replication and degradation of one molecular species is much slower than those of the others, i.e., when there is a minority molecule. Here, the synergetic effect of molecular discreteness and crowding is necessary to produce the exponential growth. Otherwise, the growth curves show superexponential growth because of nonlinearity of the catalytic reactions or subexponential growth due to replication inhibition by overcrowding of molecules. Our study emphasizes that the minority molecular species in a catalytic reaction network is necessary to acquire evolvability at the primitive stage of life.

q-bio.CB↗

Boundary-Induced Pattern Formation from Uniform Temporal Oscillation

Pattern dynamics triggered by fixing a boundary is investigated. By considering a reaction-diffusion equation that has a unique spatially-uniform and limit cycle attractor under a periodic or Neumann boundary condition, and then by choosing a fixed boundary condition, we found three novel phases depending on the ratio of diffusion constants of activator to inhibitor: transformation of temporally periodic oscillation into a spatially-periodic fixed pattern, travelling wave emitted from the boundary, and aperiodic spatiotemporal dynamics. The transformation into a fixed, periodic pattern is analyzed by crossing of local nullclines at each spatial point, shifted by diffusion terms. A spatial map, then, is introduced, whose temporal sequence can reproduce the spatially periodic pattern, by replacing the time with space. The generality of the boundary-induced pattern formation as well as its relevance to biological morphogenesis is discussed.

nlin.PS↗

Formation of Dominant Mode by Evolution in Biological Systems

Constraints on changes in expression levels across all cell components imposed by the steady growth of cells have recently been discussed both experimentally and theoretically. By assuming a small environmental perturbation and considering a linear response to it, a common proportionality in such expression changes was derived and partially verified by experimental data. Here, we examined global protein expression in ${\it Escherichia coli}$ under various environmental perturbations. Remarkably they are proportional across components, even though these environmental changes are not small and cover different types of stresses, while the proportion coefficient corresponds to the change in growth rate. However, since such global proportionality is not generic to all systems under a condition of steady growth, a new conceptual framework is needed. We hypothesized that such proportionality is a result of evolution. To validate this hypothesis, we analyzed a cell model with a huge number of components that reproduces itself via a catalytic reaction network, and confirmed that the common proportionality in the concentrations of all components is shaped through evolutionary processes to maximize cell growth (and therefore fitness) under a given environmental condition. Further, we found that the concentration changes across all components in response to environmental and evolutionary changes are constrained along a one-dimensional major axis within a huge-dimensional state space. Based on these observations, we propose a theory in which high-dimensional phenotypic changes after evolution are constrained along a one-dimensional major axis that correlates with the growth rate, which can explain broad experimental and numerical results.

q-bio.PE↗

Stronger selection can slow down evolution driven by recombination on a smooth fitness landscape

Stronger selection implies faster evolution---that is, the greater the force, the faster the change. This apparently self-evident proposition, however, is derived under the assumption that genetic variation within a population is primarily supplied by mutation (i.e.\ mutation-driven evolution). Here, we show that this proposition does not actually hold for recombination-driven evolution, i.e.\ evolution in which genetic variation is primarily created by recombination rather than mutation. By numerically investigating population genetics models of recombination, migration and selection, we demonstrate that stronger selection can slow down evolution on a perfectly smooth fitness landscape. Through simple analytical calculation, this apparently counter-intuitive result is shown to stem from two opposing effects of natural selection on the rate of evolution. On the one hand, natural selection tends to increase the rate of evolution by increasing the fixation probability of fitter genotypes. On the other hand, natural selection tends to decrease the rate of evolution by decreasing the chance of recombination between immigrants and resident individuals. As a consequence of these opposing effects, there is a finite selection pressure maximizing the rate of evolution. Hence, stronger selection can imply slower evolution if genetic variation is primarily supplied by recombination.

q-bio.PE↗

Robustness of spatial patterns in buffered reaction-diffusion systems and its reciprocity with phase plasticity

Robustness of spatial pattern against perturbations is an indispensable property of developmental processes for organisms, which need to adapt to changing environments. Although specific mechanisms for this robustness have been extensively investigated, little is known about a general mechanism for achieving robustness in reaction-diffusion systems. Here, we propose a buffered reaction-diffusion system, in which active states of chemicals mediated by buffer molecules contribute to reactions, and demonstrate that robustness of the pattern wavelength is achieved by the dynamics of the buffer molecule. This robustness is analytically explained as a result of the scaling properties of the buffered system, which also lead to a reciprocal relationship between the wavelength's robustness and the plasticity of the spatial phase upon external perturbations. Finally, we explore the relevance of this reciprocity to biological systems.

nlin.AO↗

Motif Analysis for Small-Number Effects in Chemical Reaction Dynamics

The number of molecules involved in a cell or subcellular structure is sometimes rather small. In this situation, ordinary macroscopic-level fluctuations can be overwhelmed by non-negligible large fluctuations, which results in drastic changes in chemical-reaction dynamics and statistics compared to those observed under a macroscopic system (i.e., with a large number of molecules). In order to understand how salient changes emerge from fluctuations in molecular number, we here quantitatively define small-number effect by focusing on a `mesoscopic' level, in which the concentration distribution is distinguishable both from micro- and macroscopic ones, and propose a criterion for determining whether or not such an effect can emerge in a given chemical reaction network. Using the proposed criterion, we systematically derive a list of motifs of chemical reaction networks that can show small-number effects, which includes motifs showing emergence of the power law and the bimodal distribution observable in a mesoscopic regime with respect to molecule number. The list of motifs provided herein is helpful in the search for candidates of biochemical reactions with a small-number effect for possible biological functions, as well as for designing a reaction system whose behavior can change drastically depending on molecule number, rather than concentration.

q-bio.MN↗

Symbiotic Cell Differentiation and Cooperative Growth in Multicellular Aggregates

As cells grow and divide under a given environment, they become crowded and resources are limited, as seen in bacterial biofilms and multicellular aggregates. These cells often show strong interactions through exchanging chemicals, as in quorum sensing, to achieve mutualism. Here, to achieve stable division of labor, three properties are required. First, isogenous cells differentiate into several types. Second, this aggregate of distinct cell types shows better growth than that of isolated cells, by achieving division of labor. Third, this cell aggregate is robust in the number distribution of differentiated cell types. We here address how cells acquire the ability of cell differentiation and division of labor simultaneously, which is also connected with the robustness of a cell society. For this purpose, we developed a dynamical-systems model of cells consisting of chemical components with intracellular catalytic reaction dynamics. The reactions convert external nutrients into internal components for cellular growth, and the divided cells interact via chemical diffusion. We found that cells sharing an identical catalytic network spontaneously differentiate via induction from cell-cell interactions, and then achieve division of labor, enabling a higher growth rate than that in the unicellular case. This symbiotic differentiation emerged for a class of reaction networks with limited resources and strong cell-cell interactions. Then, robustness in the cell type distribution was achieved, while instability of collective growth could emerge even among the cooperative cells when the internal reserves of products were dominant. The present mechanism is simple and general as a natural result of interacting cells with resource limitation, and is consistent with the observed behaviors and forms of several aggregates of unicellular organisms.

q-bio.CB↗

Hierarchical Prisoner's Dilemma in Hierarchical Public-Goods Game

The dilemma in cooperation is one of the major concerns in game theory. In a public-goods game, each individual pays a cost for cooperation, or to prevent defection, and receives a reward from the collected cost in a group. Thus, defection is beneficial for each individual, while cooperation is beneficial for the group. Now, groups (say, countries) consisting of individual players also play games. To study such a multi-level game, we introduce a hierarchical public-goods (HPG) game in which two groups compete for finite resources by utilizing costs collected from individuals in each group. Analyzing this HPG game, we found a hierarchical prisoner's dilemma, in which groups choose the defection policy (say, armaments) as a Nash strategy to optimize each group's benefit, while cooperation optimizes the total benefit. On the other hand, for each individual within a group, refusing to pay the cost (say, tax) is a Nash strategy, which turns to be a cooperation policy for the group, thus leading to a hierarchical dilemma. Here, the reward received by one group increases with the population, as does the collected cost. In spite of this, we find that there exists an optimal group size that maximizes its payoff. Furthermore, when the population asymmetry between two groups is large, a smaller group will choose a cooperation policy (say, disarmament) to avoid excessive response from the larger group, which leads to the resolution of the prisoner's dilemma between the groups. The relevance of the HPG game to policy selection in society and the optimal size in human or animal groups are discussed accordingly.

physics.soc-ph↗

Theory for transitions between log and stationary phases: universal laws for lag time

Quantitative characterization of bacterial growth has gathered substantial attention since Monod's pioneering study. Theoretical and experimental work has uncovered several laws for describing the log growth phase, in which the number of cells grows exponentially. However, microorganism growth also exhibits lag, stationary, and death phases under starvation conditions, in which cell growth is highly suppressed, while quantitative laws or theories for such phases are underdeveloped. In fact, models commonly adopted for the log phase that consist of autocatalytic chemical components, including ribosomes, can only show exponential growth or decay in a population, and phases that halt growth are not realized. Here, we propose a simple, coarse-grained cell model that includes inhibitor molecule species in addition to the autocatalytic active protein. The inhibitor forms a complex with active proteins to suppress the catalytic process. Depending on the nutrient condition, the model exhibits the typical transition among the lag, log, stationary, and death phases. Furthermore, the lag time needed for growth recovery after starvation follows the square root of the starvation time and is inverse to the maximal growth rate, in agreement with experimental observations. Moreover, the distribution of lag time among cells shows an exponential tail, also consistent with experiments. Our theory further predicts strong dependence of lag time upon the speed of substrate depletion, which should be examined experimentally. The present model and theoretical analysis provide universal growth laws beyond the log phase, offering insight into how cells halt growth without entering the death phase.

physics.bio-ph↗

Discreteness-induced transitions in multi-body reaction systems

A decrease in system size can induce qualitatively different behavior compared to the macroscopic behavior of the corresponding large-size system. The mechanisms of this transition, which is known as the small-size transition, can be attributed to either a relative increase in the noise intensity or to the discreteness of the state space due to the small system size. The former mechanism has been intensively investigated using several toy and realistic models. However, the latter has rarely been analyzed and is sometimes confused with the former, because a toy model that extracts the essence of the discreteness-induced transition mechanism is lacking. In this work, we propose a 1- and 3-body reaction system as a minimal model of the discreteness-induced transition and derive the conditions under which this transition occurs in more complex systems. This work enriches our understanding of the influence of small system size on system behavior.

cond-mat.stat-mech↗

Chaotic Griffiths Phase with Anomalous Lyapunov Spectra in Coupled Map Networks

Dynamics of coupled chaotic oscillators on a network are studied using coupled maps. Within a broad range of parameter values representing the coupling strength or the degree of elements, the system repeats formation and split of coherent clusters. The distribution of the cluster size follows a power law with the exponent $α$, which changes with the parameter values. The number of positive Lyapunov exponents and their spectra are scaled anomalously with the power of the system size with the exponent $β$, which also changes with the parameters. The scaling relation $α\sim 2(β+1)$ is uncovered, which seems to be universal independent of parameters and networks.

nlin.CD↗

Boundary-Induced Pattern Formation from Temporal Oscillation: Spatial Map Analysis

Boundary-induced pattern formation from a spatially uniform state is investigated using one-dimensional reaction-diffusion equations. The temporal oscillation is successively transformed into a spatially periodic pattern, triggered by diffusion from the fixed boundary. We introduced a spatial map, whose temporal sequence, under selection criteria from multiple stationary solutions, can completely reproduce the emergent pattern, by replacing the time with space. The relationship of the pattern wavelength with the period of oscillation is also obtained. The generality of the pattern selection process and algorithm is discussed with possible relevance to biological morphogenesis.

nlin.PS↗

Reciprocity Between Robustness of Period and Plasticity of Phase in Biological Clocks

Circadian clocks exhibit the robustness of period and plasticity of phase against environmental changes such as temperature and nutrient conditions. Thus far, however, it is unclear how both are simultaneously achieved. By investigating distinct models of circadian clocks, we demonstrate reci- procity between robustness and plasticity: higher robustness in the period implies higher plasticity in the phase, where changes in period and in phase follow a linear relationship with a negative coef- ficient. The robustness of period is achieved by the adaptation on the limit cycle via a concentration change of a buffer molecule, whose temporal change leads to a phase shift following a shift of the limit-cycle orbit in phase space. Generality of reciprocity in clocks with the adaptation mechanism is confirmed with theoretical analysis of simple models, while biological significance is discussed.

q-bio.MN↗

Requirements for efficient cell-type proportioning: regulatory timescales, stochasticity and lateral inhibition

The proper functioning of multicellular organisms requires the robust establishment of precise proportions between distinct cell-types. This developmental differentiation process typically involves intracellular regulatory and stochastic mechanisms to generate cell-fate diversity as well as intercellular mechanisms to coordinate cell-fate decisions at tissue level. We thus surmise that key insights about the developmental regulation of cell-type proportion can be captured by the modeling study of clustering dynamics in population of inhibitory-coupled noisy bistable systems. This general class of dynamical system is shown to exhibit a very stable two-cluster state, but also frustrated relaxation, collective oscillations or steady-state hopping which prevents from timely and reliably reaching a robust and well-proportioned clustered state. To circumvent these obstacles or to avoid fine-tuning, we highlight a general strategy based on dual-time positive feedback loops, such as mediated through transcriptional versus epigenetic mechanisms, which improves proportion regulation by coordinating early and flexible lineage priming with late and firm commitment. This result sheds new light on the respective and cooperative roles of multiple regulatory feedback, stochasticity and lateral inhibition in developmental dynamics.

q-bio.CB↗

Enzyme oscillation can enhance the thermodynamic efficiency of cellular metabolism: Consequence of anti-phase coupling between reaction flux and affinity

Cells generally convert nutrient resources to useful products via energy transduction. Accordingly, the thermodynamic efficiency of this conversion process is one of the most essential characteristics of living organisms. However, although these processes occur under conditions of dynamic metabolism, most studies of cellular thermodynamic efficiency have been restricted to examining steady states; thus, the relevance of dynamics to this efficiency has not yet been elucidated. Here, we develop a simple model of metabolic reactions with anabolism-catabolism coupling catalysed by enzymes. Through application of external oscillation in the enzyme abundances, the thermodynamic efficiency of metabolism was found to be improved. This result is in strong contrast with that observed in the oscillatory input, in which the efficiency always decreased with oscillation. This improvement was effectively achieved by separating the anabolic and catabolic reactions, which tend to disequilibrate each other, and taking advantage of the temporal oscillations so that each of the antagonistic reactions could progress near equilibrium. In this case, anti-phase oscillation between the reaction flux and chemical affinity through oscillation of enzyme abundances is essential. This improvement was also confirmed in a model capable of generating autonomous oscillations in enzyme abundances. Finally, the possible relevance of the improvement in thermodynamic efficiency is discussed with respect to the potential for manipulation of metabolic oscillations in microorganisms.

physics.bio-ph↗