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基因调控网络中的运输调控建模。

Modeling Transport Regulation in Gene Regulatory Networks.

机构信息

Department of Mathematics, University of Nevada, Reno, NV, USA.

Department of Mathematical Sciences, Montana State University, Bozeman, MT, USA.

出版信息

Bull Math Biol. 2022 Jul 13;84(8):89. doi: 10.1007/s11538-022-01035-1.

Abstract

A gene regulatory network summarizes the interactions between a set of genes and regulatory gene products. These interactions include transcriptional regulation, protein activity regulation, and regulation of the transport of proteins between cellular compartments. DSGRN is a network modeling approach that builds on traditions of discrete-time Boolean models and continuous-time switching system models. When all interactions are transcriptional, DSGRN uses a combinatorial approximation to describe the entire range of dynamics that is compatible with network structure. Here we present an extension of the DGSRN approach to transport regulation across a boundary between compartments, such as a cellular membrane. We illustrate our approach by searching a model of the p53-Mdm2 network for the potential to admit two experimentally observed distinct stable periodic cycles.

摘要

基因调控网络总结了一组基因和调控基因产物之间的相互作用。这些相互作用包括转录调控、蛋白质活性调控以及蛋白质在细胞区室之间运输的调控。DSGRN 是一种网络建模方法,它建立在离散时间布尔模型和连续时间切换系统模型的传统基础上。当所有相互作用都是转录时,DSGRN 使用组合逼近来描述与网络结构兼容的整个动力学范围。在这里,我们将 DSGRN 方法扩展到跨越细胞区室之间边界(如细胞膜)的运输调节。我们通过在 p53-Mdm2 网络模型中搜索,展示了我们的方法,以寻找可能存在两种实验观察到的不同稳定周期的潜力。

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