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具有耦合随机基因网络的细胞组织二维模型的动力学

Dynamics of a two-dimensional model of cell tissues with coupled stochastic gene networks.

作者信息

Ribeiro Andre S

机构信息

Institute of Signal Processing, Tampere University of Technology, P.O. Box 553, 33101 Tampere, Finland.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2007 Nov;76(5 Pt 1):051915. doi: 10.1103/PhysRevE.76.051915. Epub 2007 Nov 20.

Abstract

Gene expression and differentiation were shown to be stochastic processes. However, cells in a tissue can coordinate their behavior, including gene expression and differentiation pathways choice. A tissue of coupled cells is modeled as a two-dimensional regular square lattice of identical cells, each a three-dimensional compartment with a gene regulatory network (GRN) and a toggle switch (TS). The dynamics is driven by a delayed stochastic simulation algorithm, nearest neighbor cells are coupled by normally distributed time delayed reactions allowing interchange of proteins, and gene expression is a multiple time delayed reaction. It is defined the coupling strength (C), to characterize the lattice structure as a function of the rate constants of the reactions coupling nearest neighbor cells. Conditions are investigated for the emergence of synchronization and stable differentiation of cells within a tissue. From the time series of the cells GRNs, the tissue dynamical stability (S) is computed from the average toggling period of each GRN. The synchronization of cells' proteins expression levels is measured by their time series entropy (H). It is shown that the tissue goes through various dynamical regimes as C is increased, by measuring H and S . For null C, the cells GRNs toggle asynchronously. For weak C, cells synchronize by regions of space. Increasing C, the tissue becomes homogeneously synchronous. As C is further increased, S goes through a phase transition, from synchronized toggling to stable, where all cells produce one and the same protein. Finally, increasing C even further, a new stable state emerges where both genes of all cells are expressed and bistability is lost. This state, resembling an infinitely long transient, is an emergent behavior not observable in a single TS. The results provide an explanation of how cells with bistable GRNs, inherently stochastic, can synchronize or uniformly differentiate into stable states, by interacting with nearest neighbors.

摘要

基因表达和分化被证明是随机过程。然而,组织中的细胞可以协调它们的行为,包括基因表达和分化途径的选择。将耦合细胞组织建模为相同细胞的二维规则正方形晶格,每个细胞都是一个具有基因调控网络(GRN)和切换开关(TS)的三维隔室。动力学由延迟随机模拟算法驱动,最近邻细胞通过允许蛋白质交换的正态分布时间延迟反应进行耦合,并且基因表达是多次延迟反应。定义耦合强度(C),以根据耦合最近邻细胞的反应速率常数来表征晶格结构。研究了组织内细胞同步和稳定分化出现的条件。从细胞GRN的时间序列中,根据每个GRN的平均切换周期计算组织动态稳定性(S)。细胞蛋白质表达水平的同步性通过它们的时间序列熵(H)来衡量。结果表明,通过测量H和S,随着C的增加,组织会经历各种动态状态。对于零C,细胞GRN异步切换。对于弱C,细胞按空间区域同步。随着C增加,组织变得均匀同步。当C进一步增加时,S经历一个相变,从同步切换到稳定,此时所有细胞产生一种相同的蛋白质。最后,进一步增加C,出现一种新的稳定状态,其中所有细胞的两个基因都表达,双稳态消失。这种状态类似于无限长的瞬态,是在单个TS中不可观察到的涌现行为。这些结果解释了具有双稳态GRN且本质上随机的细胞如何通过与最近邻细胞相互作用来同步或均匀分化为稳定状态。

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