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集胞藻PCC 6803在酸胁迫下基因网络的生物计算构建

Biocomputional construction of a gene network under acid stress in Synechocystis sp. PCC 6803.

作者信息

Li Yi, Rao Nini, Yang Feng, Zhang Ying, Yang Yang, Liu Han-ming, Guo Fengbiao, Huang Jian

机构信息

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

Res Microbiol. 2014 Jul-Aug;165(6):420-8. doi: 10.1016/j.resmic.2014.04.004. Epub 2014 Apr 28.

Abstract

Acid stress is one of the most serious threats that cyanobacteria have to face, and it has an impact at all levels from genome to phenotype. However, very little is known about the detailed response mechanism to acid stress in this species. We present here a general analysis of the gene regulatory network of Synechocystis sp. PCC 6803 in response to acid stress using comparative genome analysis and biocomputational prediction. In this study, we collected 85 genes and used them as an initial template to predict new genes through co-regulation, protein-protein interactions and the phylogenetic profile, and 179 new genes were obtained to form a complete template. In addition, we found that 11 enriched pathways such as glycolysis are closely related to the acid stress response. Finally, we constructed a regulatory network for the intricate relationship of these genes and summarize the key steps in response to acid stress. This is the first time a bioinformatic approach has been taken systematically to gene interactions in cyanobacteria and the elaboration of their cell metabolism and regulatory pathways under acid stress, which is more efficient than a traditional experimental study. The results also provide theoretical support for similar research into environmental stresses in cyanobacteria and possible industrial applications.

摘要

酸胁迫是蓝藻必须面对的最严重威胁之一,它对从基因组到表型的各个层面都有影响。然而,对于该物种对酸胁迫的详细响应机制却知之甚少。我们在此利用比较基因组分析和生物计算预测,对集胞藻PCC 6803响应酸胁迫的基因调控网络进行了全面分析。在本研究中,我们收集了85个基因,并将其作为初始模板,通过共调控、蛋白质-蛋白质相互作用和系统发育谱来预测新基因,共获得179个新基因,从而形成一个完整的模板。此外,我们发现糖酵解等11条富集途径与酸胁迫响应密切相关。最后,我们构建了这些基因复杂关系的调控网络,并总结了响应酸胁迫的关键步骤。这是首次系统地采用生物信息学方法研究蓝藻中的基因相互作用以及酸胁迫下其细胞代谢和调控途径,比传统实验研究更高效。研究结果也为蓝藻环境胁迫的类似研究及可能的工业应用提供了理论支持。

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