Understanding inhibition of viral proteins on type I IFN signaling pathways with modeling and optimization
文献类型：期刊论文
| 作者 | Zou, Xiufen2; Xiang, Xueshuang3; Chen, Yan1; Peng, Tao2; Luo, Xuelian1; Pan, Zishu1 |
| 刊名 | JOURNAL OF THEORETICAL BIOLOGY
 |
| 出版日期 | 2010-08-21 |
| 卷号 | 265期号:4页码:691-703 |
| 关键词 | Mathematical model Genetic algorithm Signaling pathway Type I interferons Virus |
| ISSN号 | 0022-5193 |
| DOI | 10.1016/j.jtbi.2010.05.001 |
| 英文摘要 | The interferon system provides a powerful and universal intracellular defense mechanism against viruses. As one part of their survival strategies, many viruses have evolved mechanisms to counteract the host type I interferon (IFN-alpha/beta) responses. In this study, we attempt to investigate virus- and double-strand RNA (dsRNA)-triggered type I IFN signaling pathways and understand the inhibition of IFN-alpha/beta induction by viral proteins using mathematical modeling and quantitative analysis. Based on available literature and our experimental data, we develop a mathematical model of virus- and dsRNA-triggered signaling pathways leading to type I IFN gene expression during the primary response, and use the genetic algorithm to optimize all rate constants in the model. The consistency between numerical simulation results and biological experimental data demonstrates that our model is reasonable. Further, we use the model to predict the following phenomena: (I) the dose-dependent inhibition by classical swine fever virus (CSFV) N(pro) or E(rns) protein is observed at a low dose and can reach a saturation above a certain dose, not an increase; (2) E(rns) and N(pro) have no synergic inhibitory effects on IFN-beta induction; (3) the different characters in an important transcription factor, phosphorylated IRF3 (IRF3p), are exhibited because N(pro) or E(rns) counteracted dsRNA- and virus-triggered IFN-beta induction by targeting the different molecules in the signaling pathways and (4) N(pro) inhibits the IFN-beta expression not only by interacting with IFR3 but also by affecting its complex with MITA. Our approaches help to gain insight into system properties and rational therapy design, as well as to generate hypotheses for further research. (C) 2010 Elsevier Ltd. All rights reserved. |
| 资助项目 | Chinese National Basic Research Program (973 program)[2010CB911803] ; Chinese National Natural Science Foundation[30670083] ; Chinese National Natural Science Foundation[30771597] |
| WOS研究方向 | Life Sciences & Biomedicine - Other Topics ; Mathematical & Computational Biology |
| 语种 | 英语 |
| WOS记录号 | WOS:000280445300022 |
| 出版者 | ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD |
| 源URL | [http://ir.amss.ac.cn/handle/2S8OKBNM/9470]  |
| 专题 | 中国科学院数学与系统科学研究院 |
| 通讯作者 | Pan, Zishu |
| 作者单位 | 1.Wuhan Univ, State Key Lab Virol, Coll Life Sci, Wuhan 430072, Peoples R China 2.Wuhan Univ, Sch Math & Stat, Wuhan 430072, Peoples R China 3.Chinese Acad Sci, Acad Math & Syst Sci, Inst Computat Math, Beijing 100080, Peoples R China |
| 推荐引用方式 GB/T 7714 | Zou, Xiufen,Xiang, Xueshuang,Chen, Yan,et al. Understanding inhibition of viral proteins on type I IFN signaling pathways with modeling and optimization[J]. JOURNAL OF THEORETICAL BIOLOGY,2010,265(4):691-703. |
| APA | Zou, Xiufen,Xiang, Xueshuang,Chen, Yan,Peng, Tao,Luo, Xuelian,&Pan, Zishu.(2010).Understanding inhibition of viral proteins on type I IFN signaling pathways with modeling and optimization.JOURNAL OF THEORETICAL BIOLOGY,265(4),691-703. |
| MLA | Zou, Xiufen,et al."Understanding inhibition of viral proteins on type I IFN signaling pathways with modeling and optimization".JOURNAL OF THEORETICAL BIOLOGY 265.4(2010):691-703. |
入库方式： OAI收割
来源：数学与系统科学研究院
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