Cases Ildefonso, Ussery David W, de Lorenzo Víctor
Centro Nacional de Biotecnología, CSIC Campus de Cantoblanco, 28049 Madrid, Spain.
Environ Microbiol. 2003 Dec;5(12):1281-93. doi: 10.1111/j.1462-2920.2003.00528.x.
sigma54 is unique among the bacterial sigma factors. Besides not being related in sequence with the rest of such factors, its mechanism of transcription initiation is completely different and requires the participation of a transcription activator. In addition, whereas the rest of the alternative sigma factors use to be involved in transcription of somehow related biological functions, this is not the case for sigma54 and many different and unrelated genes have been shown to be transcribed from sigma54-dependent promoters, ranging from flagellation, to utilization of several different carbon and nitrogen sources, or alginate biosynthesis. These genes have been characterized in many different bacterial species and, only until recently with the arrival of complete genome sequences, we have been able to look at the sigma54 functional role from a genomic perspective. Aided by computational methods, the sigma54 regulon has been studied both in Escherichia coli, Salmonella typhimurium and several species of the Rhizobiaceae. Here we present the analysis of the sigma54 regulon (sigmulon) in the complete genome of Pseudomonas putida KT2440. We have developed an improved method for the prediction of sigma54-dependent promoters which combines the scores of sigma54-RNAP target sequences and those of activator binding sites. In combination with other evidence obtained from the chromosomal context and the similarity with closely related bacteria, we have been able to predict more than 80% of the sigma54-dependent promoters of P. putida with high confidence. Our analysis has revealed new functions for sigma54 and, by means of comparative analysis with the previous studies, we have drawn a potential mechanism for the evolution of this regulatory system.
σ54在细菌σ因子中独具特色。它不仅在序列上与其他此类因子毫无关联,其转录起始机制也全然不同,需要转录激活因子的参与。此外,其他替代σ因子往往参与某种相关生物学功能的转录,而σ54并非如此,许多不同且不相关的基因已被证明可从依赖σ54的启动子转录,范围涵盖鞭毛形成、多种不同碳源和氮源的利用,或藻酸盐生物合成。这些基因已在许多不同细菌物种中得到表征,直到最近随着完整基因组序列的出现,我们才得以从基因组角度审视σ54的功能作用。借助计算方法,已在大肠杆菌、鼠伤寒沙门氏菌和几种根瘤菌科物种中研究了σ54调控子。在此,我们展示了对恶臭假单胞菌KT2440完整基因组中σ54调控子(σ54操纵子)的分析。我们开发了一种改进方法来预测依赖σ54的启动子,该方法结合了σ54 - RNA聚合酶靶序列得分和激活因子结合位点得分。结合从染色体背景获得的其他证据以及与密切相关细菌的相似性,我们能够高度自信地预测恶臭假单胞菌80%以上依赖σ54的启动子。我们的分析揭示了σ54的新功能,并且通过与先前研究的比较分析,我们得出了该调控系统进化的潜在机制。