A simplified model of chromatin dynamics drives differentiation process in Boolean models of GRN

Michele Braccini, A. Roli, M. Villani, Sara Montagna, R. Serra
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引用次数: 5

Abstract

Cellular types of multicellular organisms are the stable results of complex intertwined processes that occur in biological cells. Among the many others, chromatin dynamics significantly contributes—by modulating access to genes—to differential gene expression, and ultimately to determine cell types. Here, we propose a dynamical model of differentiation based on a simplified bio-inspired methylation mechanism in Boolean models of GRNs. Preliminary results show that, as the number of methylated nodes increases, there is a decrease in attractor number and networks tend to assume dynamical behaviours typical of ordered ensembles. At the same time, results show that this mechanism does not affect the possibility of generating path dependent differentiation: cell types determined by the specific sequence of methylated genes.
一个简化的染色质动力学模型驱动GRN布尔模型的分化过程
多细胞生物的细胞类型是发生在生物细胞中复杂交织过程的稳定结果。在许多其他因素中,染色质动力学通过调节对基因的访问,显著地促进了差异基因表达,并最终决定了细胞类型。在此,我们提出了一个基于简化的生物甲基化机制的grn布尔模型的分化动态模型。初步结果表明,随着甲基化节点数量的增加,吸引子数量减少,网络倾向于采取有序集成的典型动态行为。同时,结果表明,该机制不影响产生路径依赖性分化的可能性:由甲基化基因的特定序列决定的细胞类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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