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噬菌体基因调控网络的行为动力学。

Behavioral dynamics of bacteriophage gene regulatory networks.

机构信息

Institute of Mathematics and Computer Science, University of Latvia, Rainis Boulevard 29, Riga LV-1459, Latvia.

出版信息

J Bioinform Comput Biol. 2022 Oct;20(5):2250021. doi: 10.1142/S0219720022500214. Epub 2022 Sep 14.

Abstract

We present hybrid system-based gene regulatory network models for lambda, HK022, and Mu bacteriophages together with dynamics analysis of the modeled networks. The proposed lambda phage model LPH2 is based on an earlier work and incorporates more recent biological assumptions about the underlying gene regulatory mechanism, HK022, and Mu phage models are new. All three models provide accurate representations of experimentally observed lytic and lysogenic behavioral cycles. Importantly, the models also imply that lysis and lysogeny are stable behaviors that can occur in the modeled networks. In addition, the models allow to derive switching conditions that irrevocably lead to either lytic or lysogenic behavioral cycle as well as constraints that are required for their biological feasibility. For LPH2 model the feasibility constraints place two mutually independent requirements on comparative order of cro and cI protein binding site affinities. However, HK022 model, while broadly similar, does not require any of these constraints. Biologically very different lysis-lysogeny switching mechanism of Mu phage is also accurately reproduced by its model. In general the results show that hybrid system model (HSM) hybrid system framework can be successfully applied to modeling small ([Formula: see text] gene) regulatory networks and used for comprehensive analysis of model dynamics and stable behavior regions.

摘要

我们提出了基于混合系统的 lambda、HK022 和 Mu 噬菌体基因调控网络模型,并对所建模型的动力学进行了分析。所提出的 lambda 噬菌体模型 LPH2 基于早期的工作,并结合了关于潜在基因调控机制的最新生物学假设,而 HK022 和 Mu 噬菌体模型是新的。这三个模型都提供了对实验观察到的裂解和溶原性行为周期的准确描述。重要的是,这些模型还表明裂解和溶原是可以在模型网络中发生的稳定行为。此外,这些模型还可以推导出不可逆地导致裂解或溶原行为周期的切换条件,以及实现其生物学可行性所需的约束条件。对于 LPH2 模型,可行性约束对 cro 和 cI 蛋白结合位点亲和力的比较顺序提出了两个相互独立的要求。然而,HK022 模型虽然大致相似,但不需要任何这些约束条件。Mu 噬菌体的裂解-溶原转换机制在生物学上非常不同,但其模型也能准确再现。总的来说,结果表明,混合系统模型(HSM)的混合系统框架可以成功地应用于小([Formula: see text]基因)调控网络的建模,并用于模型动力学和稳定行为区域的全面分析。

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