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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Cross-regulatory network in Pseudomonas aeruginosa biofilm genes and TiO 2 anatase induced molecular perturbations in key proteins unraveled by a systems biology approach
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Cross-regulatory network in Pseudomonas aeruginosa biofilm genes and TiO 2 anatase induced molecular perturbations in key proteins unraveled by a systems biology approach

机译:铜绿假单胞菌铜绿假单胞菌基因的跨调控网络和TiO 2锐钛矿诱导由系统生物学方法解开的关键蛋白质中的分子扰动

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摘要

Abstract A systems biology approach was used to study all the biofilm related genes of P. aeruginosa PAO1, and the interaction of titanium dioxide (TiO 2 ) anatase with biofilm related proteins. Among the 71 genes, the interactions of all the nodal pairs were extracted by STRING 10.5 database. The inter-relationship among these genes was predicted by constructing complete PPI network and visualized in Cytoscape v 3.4.0. Total number of nodes of the network was found to be 335 and edges were 795. The network was further investigated for its clusters and the best cluster was further analyzed for the hub proteins which significantly contribute in cross-regulation of the biofilm related process. The hub proteins were identified based on four topological parameters of degree, closeness, betweeness and radiality. Four major hub proteins of P. aeruginosa PAO1 were identified to be algD, gacS, rpoS and rpoN which were common in all the hubs. Further, we have also elucidated the probable mechanism of TiO 2 interaction with P. aeruginosa PAO1 at molecular level. Using STITCH server, the major target gene of TiO 2 was identified as kat A which also appeared commonly in our main dataset and this gene has been focused for the further study because of its unique common appearance in gene–gene network as well as gene-anatase network. The direct interacting partners of katA were found to be dnaK, hfq, rpoS and rpoA . Based on these findings and available gene regulatory information, probable TiO 2 interacting cascade has been represented. This in silico study of P. aeruginosa PAO1 biofilm genes and the interaction of protein products with TiO 2 might be significant to understand the perspective pathogenic resistance as well as the toxicity research pertaining to nanoparticles. Highlights ? Elucidation of gene interaction network in Pseudomonas aeruginosa biofilm formation. ? Interaction gene hubs are centrally regulated by alg D, gac S, rpo S and rpo N. ? Major target of TiO 2 NP is kat A and the direct interacting partners are dna K, hfq , rpo S and rpo A. ? Molecular changes in Pseudomonas aeruginosa during interaction with TiO 2 NP are proposed.
机译:摘要使用系统生物学方法研究了铜绿假单胞菌的所有生物膜相关基因,以及二氧化钛(TiO 2)锐钛矿与生物膜相关蛋白的相互作用。在71个基因中,通过String 10.5数据库提取所有节点对的相互作用。通过构建完整的PPI网络并在Cytoscape V 3.4.0中可视化来预测这些基因之间的相互关系。发现网络的节点总数为335,边缘为795.进一步研究了其簇,并进一步分析了最佳聚类,用于枢纽蛋白质显着促进生物膜相关过程的交叉调节。基于四个拓扑参数,接近度,辐射性和辐射性的四个拓扑参数鉴定了轮毂蛋白。鉴定了P.铜绿假单胞菌PAO1的四个主要轮毂蛋白是藻类,GACS,RPO和RPON,其在所有枢纽中常见。此外,我们还阐明了分子水平的TiO 2与铜绿假单胞菌Pao1相互作用的可能机制。使用针脚服务器,TiO 2的主要目标基因被鉴定为KAT A,其在我们的主要数据集中也常见,并且该基因已经专注于进一步的研究,因为其基因基因网络的独特常见外观以及基因 - Anatase网络。发现Kata的直接互动伴侣是DNAK,HFQ,RPO和RPOA。基于这些发现和可用的基因监管信息,已表示可能的TiO 2相互作用的级联。这在P.铜绿假单胞菌Pao1生物膜基因的基石研究中,蛋白质产品与TiO 2的相互作用可能是显着的,了解术语致病性能以及纳米颗粒的毒性研究。强调 ?铜绿假单胞菌生物膜形成基因相互作用网络的阐明。还相互作用基因集线器由ALG D,GAC S,RPO S和RPO N中心调节。 TiO 2 NP的主要目标是KAT A,直接互动伴侣是DNA K,HFQ,RPO S和RPO A.提出了与TiO 2 NP相互作用期间假单胞菌铜绿假单胞菌的分子变化。

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