arXiv subjects

Chikara Furusawa

Publications and source records attributed to Chikara Furusawa.

17 recordsLinked to original sources

arXiv2025

Population dynamics of generalist/specialist strategies in the feast-famine cycles

Microbial populations exhibit a broad spectrum of nutrient utilization strategies, ranging from strategies utilizing diverse nutrients, called "generalists," to those being highly adapted to specific nutrients, called "specialists." The mathematical conditions for the diversification of nutrient utilization strategies are central questions in theoretical ecology. Previous studies have shown that trade-offs among different resource utilization functions that cells cannot utilize broad types of substrates at near-maximum speed are crucial for the emergence of diverse strategies. However, in natural settings, nutrient availability often fluctuates over time, imposing additional trade-offs on cells. Cells that grow rapidly under nutrient-rich conditions will suffer a higher death rate under nutrient-poor conditions, creating a growth-death trade-off that intersects with the classical resource-use trade-off. Here, we introduce a unified mathematical model that simultaneously incorporates the resource-use trade-off and the growth-death trade-off. The nutrient supply was modeled as discrete stochastic events, capturing realistic temporal fluctuations. We show that the relative balance between growth and death rates critically influences the dominance of either generalist or specialist strategies. Specifically, under conditions of high average growth rates among different environments and a weak trade-off between growth and death rates, generalists prevail. In contrast, when the growth-death trade-off is intense, specialists emerge as the dominant strategy. Our findings reveal that accounting for the growth-death trade-off is crucial for understanding how microbial communities adapt and evolve in temporally varying environments.

q-bio.PE↗

arXiv2023

Prediction of Cross-Fitness for Adaptive Evolution to Different Environmental Conditions: Consequence of Phenotypic Dimensional Reduction

How adaptive evolution to one environmental stress improves or suppresses adaptation to another is an important problem in evolutionary biology. For instance, in microbiology, the evolution of bacteria to be resistant to different antibiotics is a critical issue that has been investigated as cross-resistance. In fact, recent experiments on bacteria have suggested that the cross-resistance of their evolution to various stressful environments can be predicted by the changes to their transcriptome upon application of stress. However, there are no studies so far that explain a possible theoretical relationship between cross-resistance and changes in the transcriptome, which causes high-dimensional changes to cell phenotype. Here, we show that a correlation exists between fitness change in stress tolerance evolution and response to the environment, using a cellular model with a high-dimensional phenotype and establishing the relationship theoretically. The present results allow for the prediction of evolution from transcriptome information in response to different stresses before evolution. The relevance of this to microbiological evolution experiments is discussed.

q-bio.PE↗

arXiv2022

Rare-Event Sampling Analysis Uncovers the Fitness Landscape of the Genetic Code

The genetic code refers to a rule that maps 64 codons to 20 amino acids. Nearly all organisms, with few exceptions, share the same genetic code, the standard genetic code (SGC). While it remains unclear why this universal code has arisen and been maintained during evolution, it may have been preserved under selection pressure. Theoretical studies comparing the SGC and numerically created hypothetical random genetic codes have suggested that the SGC has been subject to strong selection pressure for being robust against translation errors. However, these prior studies have searched for random genetic codes in only a small subspace of the possible code space due to limitations in computation time. Thus, how the genetic code has evolved, and the characteristics of the genetic code fitness landscape, remain unclear. By applying multicanonical Monte Carlo, an efficient rare-event sampling method, we efficiently sampled random codes from a much broader random ensemble of genetic codes than in previous studies, estimating that only one out of every $10^{20}$ random codes is more robust than the SGC. This estimate is significantly smaller than the previous estimate, one in a million. We also characterized the fitness landscape of the genetic code that has four major fitness peaks, one of which includes the SGC. Furthermore, genetic algorithm analysis revealed that evolution under such a multi-peaked fitness landscape could be strongly biased toward a narrow peak, in an evolutionary path-dependent manner.

q-bio.PE↗

arXiv2021

Direction and Constraint in Phenotypic Evolution: Dimension Reduction and Global Proportionality in Phenotype Fluctuation and Responses

A macroscopic theory for describing cellular states during steady-growth is presented, which is based on the consistency between cellular growth and molecular replication, as well as the robustness of phenotypes against perturbations. Adaptive changes in high-dimensional phenotypes were shown to be restricted within a low-dimensional slow manifold, from which a macroscopic law for cellular states was derived, which was confirmed by adaptation experiments on bacteria under stress. Next, the theory was extended to phenotypic evolution, leading to proportionality between phenotypic responses against genetic evolution and environmental adaptation. The link between robustness to noise and mutation, as a result of robustness in developmental dynamics to perturbations, showed proportionality between phenotypic plasticity by genetic changes and by environmental noise. Accordingly, directionality and constraint in phenotypic evolution was quantitatively formulated in terms of phenotypic fluctuation and the response against environmental change. The evolutionary relevance of slow modes in controlling high-dimensional phenotypes is discussed.

q-bio.PE↗

arXiv2017

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↗

arXiv2015

Pluripotency, differentiation, and reprogramming: A gene expression dynamics model with epigenetic feedback regulation

Characterization of pluripotent states, in which cells can both self-renew and differentiate, and the irreversible loss of pluripotency are important research areas in developmental biology. In particular, an understanding of these processes is essential to the reprogramming of cells for biomedical applications, i.e., the experimental recovery of pluripotency in differentiated cells. Based on recent advances in dynamical-systems theory for gene expression, we propose a gene-regulatory-network model consisting of several pluripotent and differentiation genes. Our results show that cellular-state transition to differentiated cell types occurs as the number of cells increases, beginning with the pluripotent state and oscillatory expression of pluripotent genes. Cell-cell signaling mediates the differentiation process with robustness to noise, while epigenetic modifications affecting gene expression dynamics fix the cellular state. These modifications ensure the cellular state to be protected against external perturbation, but they also work as an epigenetic barrier to recovery of pluripotency. We show that overexpression of several genes leads to the reprogramming of cells, consistent with the methods for establishing induced pluripotent stem cells. Our model, which involves the inter-relationship between gene expression dynamics and epigenetic modifications, improves our basic understanding of cell differentiation and reprogramming.

q-bio.MN↗

arXiv2015

Global Relationships in Fluctuation and Response in Adaptive Evolution

Cells generally change their internal state to adapt to an environmental change, and accordingly evolve in response to the new conditions. This process involves phenotypic changes that occur over several different time scales, ranging from faster environmental adaptation without a corresponding change in the genomic sequence to slower evolutionary dynamics involving genetic mutations and subsequent selection. In this regard, a question arises as to whether there are any relationships between such phenotypic changes over the different time scales at which adaptive evolution occurs. In this study, we analyzed simulated adaptive evolution in a simple cell model, and found that proportionality between concentration changes in adaptation and evolution over all components, and the proportion coefficients were closely linked to the change in the growth rate of a cell. Furthermore, we demonstrated that the phenotypic variances in component concentrations due to (non-genetic) noise and genomic alternations are proportional across all components. These global relationships in cellular states were also supported by phenomenological theory and transcriptome analysis of laboratory evolution in {\it Escherichia coli}. These findings provide a basis for the development of a quantitative theory of plasticity and robustness, and to determine the general restriction of phenotypic changes imposed by evolution.

q-bio.PE↗

arXiv2014

Universal relationship in gene-expression changes for cells in steady-growth state

Cells adapt to different conditions by altering a vast number of components, which is measurable using transcriptome analysis. Given that a cell undergoing steady growth is constrained to sustain each of its internal components, the abundance of all the components in the cell has to be roughly doubled during each cell division event. From this steady-growth constraint, expression of all genes is shown to change along a one-parameter curve in the state space in response to the environmental stress. This leads to a global relationship that governs the cellular state: By considering a relatively moderate change around a steady state, logarithmic changes in expression are shown to be proportional across all genes, upon alteration of stress strength, with the proportionality coefficient given by the change in the growth rate of the cell. This theory is confirmed by transcriptome analysis of Escherichia Coli in response to several stresses.

q-bio.CB↗

arXiv2008

Consistency Principle in Biological Dynamical Systems

We propose a principle of consistency between different hierarchical levels of biological systems. Given a consistency between molecule replication and cell reproduction, universal statistical laws on cellular chemical abundances are derived and confirmed experimentally. They include a power law distribution of gene expressions, a lognormal distribution of cellular chemical abundances over cells, and embedding of the power law into the network connectivity distribution. Second, given a consistency between genotype and phenotype, a general relationship between phenotype fluctuations by genetic variation and isogenic phenotypic fluctuation by developmental noise is derived. Third, we discuss the chaos mechanism for stem cell differentiation with autonomous regulation, resulting from a consistency between cell reproduction and growth of the cell ensemble.

q-bio.CB↗

arXiv2007

A generic mechanism for adaptive growth rate regulation

How can a microorganism adapt to a variety of environmental conditions despite there exists a limited number of signal transduction machineries? We show that for any growing cells whose gene expression is under stochastic fluctuations, adaptive cellular state is inevitably selected by noise, even without specific signal transduction network for it. In general, changes in protein concentration in a cell are given by its synthesis minus dilution and degradation, both of which are proportional to the rate of cell growth. In an adaptive state with a higher growth speed, both terms are large and balanced. Under the presence of noise in gene expression, the adaptive state is less affected by stochasticity since both the synthesis and dilution terms are large, while for a non-adaptive state both the terms are smaller so that cells are easily kicked out of the original state by noise. Hence, escape time from a cellular state and the cellular growth rate are negatively correlated. This leads to a selection of adaptive states with higher growth rates, and model simulations confirm this selection to take place in general. The results suggest a general form of adaptation that has never been brought to light - a process that requires no specific machineries for sensory adaptation. The present scheme may help explain a wide range of cellular adaptive responses including the metabolic flux optimization for maximal cell growth.

q-bio.MN↗

arXiv2005

Evolutionary origin of power-laws in Biochemical Reaction Network; embedding abundance distribution into topology

The evolutionary origin of universal statistics in biochemical reaction network is studied, to explain the power-law distribution of reaction links and the power-law distributions of chemical abundances. Using cell models with catalytic reaction network, we find evidence that the power-law distribution in abundances of chemicals emerges by the selection of cells with higher growth speeds. Through the further evolution, this inhomogeneity in chemical abundances is shown to be embedded in the distribution of links, leading to the power-law distribution. These findings provide novel insights into the nature of network evolution in living cells.

q-bio.PE↗

arXiv2005

Ubiquity of Log-normal Distributions in Intra-cellular Reaction Dynamic

The discovery of two fundamental laws concerning cellular dynamics with recursive growth is reported. First, the chemical abundances measured over many cells are found to obey a log-normal distribution and second, the relationship between the average and standard deviation of the abundances is found to be linear. The ubiquity of the laws is explored both theoretically and experimentally. First by means of a model with a catalytic reaction network, the laws are shown to appear near the critical state with efficient self-reproduction. Second by measuring distributions of fluorescent proteins in bacteria cells the ubiquity of log-normal distribution of protein abundances is confirmed. Relevance of these findings to cellular function and biological plasticity is briefly discussed.

q-bio.MN↗

arXiv2002

Zipf's Law in Gene Expression

Using data from gene expression databases on various organisms and tissues, including yeast, nematodes, human normal and cancer tissues, and embryonic stem cells, we found that the abundances of expressed genes exhibit a power-law distribution with an exponent close to -1, i.e., they obey Zipf's law. Furthermore, by simulations of a simple model with an intra-cellular reaction network, we found that Zipf's law of chemical abundance is a universal feature of cells where such a network optimizes the efficiency and faithfulness of self-reproduction. These findings provide novel insights into the nature of the organization of reaction dynamics in living cells.

physics.bio-ph↗

arXiv2000

Theory of Robustness of Irreversible Differentiation in a Stem Cell System: Chaos hypothesis

Based on extensive study of a dynamical systems model of the development of a cell society, a novel theory for stem cell differentiation and its regulation is proposed as the ``chaos hypothesis''. Two fundamental features of stem cell systems - stochastic differentiation of stem cells and the robustness of a system due to regulation of this differentiation - are found to be general properties of a system of interacting cells exhibiting chaotic intra-cellular reaction dynamics and cell division, whose presence does not depend on the detail of the model. It is found that stem cells differentiate into other cell types stochastically due to a dynamical instability caused by cell-cell interactions, in a manner described by the Isologous Diversification theory. This developmental process is shown to be stable not only with respect to molecular fluctuations but also with respect to removal of cells. With this developmental process, the irreversible loss of multipotency accompanying the change from a stem cell to a differentiated cell is shown to be characterized by a decrease in the chemical diversity in the cell and of the complexity of the cellular dynamics. The relationship between the division speed and this loss of multipotency is also discussed. Using our model, some predictions that can be tested experimentally are made for a stem cell system.

nlin.AO↗

arXiv2000

Origin of complexity in multicellular organisms

Through extensive studies of dynamical system modeling cellular growth and reproduction, we find evidence that complexity arises in multicellular organisms naturally through evolution. Without any elaborate control mechanism, these systems can exhibit complex pattern formation with spontaneous cell differentiation. Such systems employ a `cooperative' use of resources and maintain a larger growth speed than simple cell systems, which exist in a homogeneous state and behave 'selfishly'. The relevance of the diversity of chemicals and reaction dynamics to the growth of a multicellular organism is demonstrated. Chaotic biochemical dynamics are found to provide the multi-potency of stem cells.

nlin.AO↗

arXiv1999

Robust and Irreversible Development in Cell Society as a General Consequence of Intra-Inter Dynamics

A dynamical systems scenario for developmental cell biology is proposed, based on numerical studies of a system with interacting units with internal dynamics and reproduction. Diversification, formation of discrete and recursive types, and rules for differentiation are found as a natural consequence of such a system. "Stem cells" that either proliferate or differentiate to different types stochastically are found to appear when intra-cellular dynamics are chaotic. Robustness of the developmental process against microscopic and macroscopic perturbations is shown to be a natural consequence of such intra-inter dynamics, while irreversibility in developmental process is discussed in terms of the gain of stability, loss of diversity and chaotic instability.

chao-dyn↗

arXiv1998

Emergence of Rules in Cell Society: Differentiation, Hierarchy, and Stability

A dynamic model for cell differentiation is studied, where cells with internal chemical reaction dynamics interact with each other and replicate. It leads to spontaneous differentiation of cells and determination, as is discussed in the isologous diversification. Following features of the differentiation are obtained: (1)Hierarchical differentiation from a ``stem'' cell to other cell types, with the emergence of the interaction-dependent rules for differentiation; (2)Global stability of an ensemble of cells consisting of several cell types, that is sustained by the emergent, autonomous control on the rate of differentiation; (3)Existence of several cell colonies with different cell-type distributions. The results provide a novel viewpoint on the origin of complex cell society, while relevance to some biological problems, especially to the hemopoietic system, is also discussed.

adap-org↗