Bobek Jan, Strakova Eva, Zikova Alice, Vohradsky Jiri
Institute of Microbiology, Academy of Sciences of the Czech Republic, Laboratory of Bioinformatics, Vídeňská 1083, 142 20 Prague 4, Czech Republic.
BMC Genomics. 2014 Dec 23;15(1):1173. doi: 10.1186/1471-2164-15-1173.
Bacterial spore germination is a developmental process during which all required metabolic pathways are restored to transfer cells from their dormant state into vegetative growth. Streptomyces are soil dwelling filamentous bacteria with complex life cycle, studied mostly for they ability to synthesize secondary metabolites including antibiotics.
Here, we present a systematic approach that analyzes gene expression data obtained from 13 time points taken over 5.5 h of Streptomyces germination. Genes whose expression was significantly enhanced/diminished during the time-course were identified, and classified to metabolic and regulatory pathways. The classification into metabolic pathways revealed timing of the activation of specific pathways during the course of germination. The analysis also identified remarkable changes in the expression of specific sigma factors over the course of germination. Based on our knowledge of the targets of these factors, we speculate on their possible roles during germination. Among the factors whose expression was enhanced during the initial part of germination, SigE is though to manage cell wall reconstruction, SigR controls protein re-aggregation, and others (SigH, SigB, SigI, SigJ) control osmotic and oxidative stress responses.
From the results, we conclude that most of the metabolic pathway mRNAs required for the initial phases of germination were synthesized during the sporulation process and stably conserved in the spore. After rehydration in growth medium, the stored mRNAs are being degraded and resynthesized during first hour. From the analysis of sigma factors we conclude that conditions favoring germination evoke stress-like cell responses.
细菌孢子萌发是一个发育过程,在此过程中,所有必需的代谢途径得以恢复,从而使细胞从休眠状态转变为营养生长状态。链霉菌是生活在土壤中的丝状细菌,具有复杂的生命周期,主要因其合成包括抗生素在内的次生代谢产物的能力而受到研究。
在此,我们提出了一种系统方法,用于分析从链霉菌萌发5.5小时内的13个时间点获得的基因表达数据。确定了在时间进程中表达显著增强/减弱的基因,并将其分类到代谢和调控途径中。代谢途径分类揭示了萌发过程中特定途径激活的时间。分析还确定了在萌发过程中特定σ因子表达的显著变化。基于我们对这些因子靶标的了解,我们推测了它们在萌发过程中的可能作用。在萌发初期表达增强的因子中,SigE被认为负责细胞壁重建,SigR控制蛋白质重新聚集,其他因子(SigH、SigB、SigI、SigJ)控制渗透压和氧化应激反应。
从结果中我们得出结论,萌发初期所需的大多数代谢途径mRNA是在孢子形成过程中合成的,并在孢子中稳定保存。在生长培养基中复水后,储存的mRNA在第一个小时内被降解并重新合成。从σ因子的分析中我们得出结论,有利于萌发的条件会引发类似应激的细胞反应。