利用转录组学数据构建铜绿假单胞菌群体感应的定量基因调控机制

Shaomin Yan, Guang Wu
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引用次数: 0

摘要

大量的转录组学数据提供了机会1)在群体水平上验证基因调控机制,这通常是从单个实验中获得的;2) 揭示群体水平的基因调控机制;3)建立定量的基因调控机制。群体感应(QS)是细菌中研究得最好的调节机制之一,它在调节细菌群体行为中发挥着重要作用,如抗生素产生、生物膜形成、生物发光、能力、结合、运动和孢子形成。铜绿假单胞菌是一种引起植物、动物和人类疾病的革兰氏阴性菌,其生物膜和耐药性已成为临床关注的焦点。铜绿假单胞菌有三个QS系统,其中一个是针对假单胞菌的。在本研究中,结合来自104篇出版物的铜绿假单胞菌转录组学数据,分析了不同实验条件下QS基因的表达。结果证明了QS基因在群体水平上的定量调控机制,包括1)根据QS相关基因的活性对其进行排序和分组;2) 定量界定单一全球监管机构的作用;3) 找出全球调节因子影响QS基因的概率以及QS基因对全球调节因子作出反应的概率;以及4)在四种类型的实验条件下搜索重叠基因。这些结果为理解群体水平上QS基因的调控提供了综合信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Building Quantitative Gene Regulatory Mechanism in Quorum Sensing in Pseudomonas aeruginosa Using Transcriptomic Data
A large amount of transcriptomic data provides opportunities 1) to verify the gene regulatory mechanism, which is usually obtained from a single experiment, at population level; 2) to uncover the gene regulatory mechanism at population level; and 3) to build a quantitatively gene regulatory mechanism. One of the best studied regulatory mechanisms in bacteria is the quorum sensing (QS), which plays an important role in regulation of bacteria population behaviors such as antibiotic production, biofilm formation, bioluminescence, competence, conjugation, motility and sporulation. Pseudomonas aeruginosa is a Gram-negative bacterium causing diseases in plants, animals, humans, and its biofilm and drug-resistance become great concerns in clinics. P. aeruginosa has three QS systems including a specific one for Pseudomonas. In this study, the transcriptomic data of P. aeruginosa were combined from 104 publications and QS gene expressions were analyzed under different experimental conditions. The results demonstrate the quantitatively regulatory mechanisms of QS genes at population level including 1) to rank and group QS-related genes according to their activity; 2) to quantitatively define the role of a single global regulator; 3) to find out the probability that a global regulator impacts QS genes and the probability that a QS gene responds to global regulators; and 4) to search for overlapped genes under four types of experimental conditions. These results provide integrative information on understanding the regulation of QS genes at population level.
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