Baraquet Claudine, Harwood Caroline S
Department of Microbiology, University of Washington, Seattle, Washington, USA.
Department of Microbiology, University of Washington, Seattle, Washington, USA
J Bacteriol. 2015 Oct 19;198(1):178-86. doi: 10.1128/JB.00539-15. Print 2016 Jan 1.
The transcription factor FleQ from Pseudomonas aeruginosa derepresses expression of genes involved in biofilm formation when intracellular levels of the second messenger cyclic diguanosine monophosphate (c-di-GMP) are high. FleQ also activates transcription of flagellar genes, and the expression of these genes is highest at low intracellular c-di-GMP. FleQ thus plays a central role in mediating the transition between planktonic and biofilm lifestyles of P. aeruginosa. Previous work showed that FleQ controls expression of the pel operon for Pel exopolysaccharide biosynthesis by converting from a repressor to an activator upon binding c-di-GMP. To explore the activity of FleQ further, we carried out DNase I footprinting at three additional biofilm gene promoters, those of psl, cdrAB, and PA2440. The expression of cdrAB, encoding a cell surface adhesin, was sufficiently responsive to FleQ to allow us to carry out in vivo promoter assays. The results showed that, similarly to our observations with the pel operon, FleQ switches from a repressor to an activator of cdrAB gene expression in response to c-di-GMP. From the footprinting data, we identified a FleQ DNA binding consensus sequence. A search for this conserved sequence in bacterial genome sequences led to the identification of FleQ binding sites in the promoters of the siaABCD operon, important for cell aggregation, and the bdlA gene, important for biofilm dispersal, in P. aeruginosa. We also identified FleQ binding sites upstream of lapA-like adhesin genes in other Pseudomonas species.
The transcription factor FleQ is widely distributed in Pseudomonas species. In all species examined, it is a master regulator of flagellar gene expression. It also regulates diverse genes involved in biofilm formation in P. aeruginosa when intracellular levels of the second messenger c-di-GMP are high. Unlike flagellar genes, biofilm-associated genes are not always easy to recognize in genome sequences. Here, we identified a consensus DNA binding sequence for FleQ. This allowed us to survey Pseudomonas strains and find new genes that are likely regulated by FleQ and possibly involved in biofilm formation.
当细胞内第二信使环二鸟苷单磷酸(c-di-GMP)水平较高时,铜绿假单胞菌的转录因子FleQ会解除对生物膜形成相关基因表达的抑制。FleQ还会激活鞭毛基因的转录,而这些基因在细胞内c-di-GMP水平较低时表达最高。因此,FleQ在介导铜绿假单胞菌浮游生活方式和生物膜生活方式之间的转变中起着核心作用。先前的研究表明,FleQ通过在结合c-di-GMP后从阻遏物转变为激活物来控制Pel胞外多糖生物合成的pel操纵子的表达。为了进一步探究FleQ的活性,我们在另外三个生物膜基因启动子(psl、cdrAB和PA2440的启动子)上进行了DNase I足迹分析。编码细胞表面黏附素的cdrAB的表达对FleQ有足够的响应,使我们能够进行体内启动子分析。结果表明,与我们对pel操纵子的观察结果类似,FleQ会响应c-di-GMP从cdrAB基因表达的阻遏物转变为激活物。根据足迹分析数据,我们确定了一个FleQ DNA结合共有序列。在细菌基因组序列中搜索这个保守序列,导致在铜绿假单胞菌中鉴定出对细胞聚集很重要的siaABCD操纵子启动子以及对生物膜分散很重要的bdlA基因启动子中的FleQ结合位点。我们还在其他假单胞菌属物种的lapA样黏附素基因上游鉴定出了FleQ结合位点。
转录因子FleQ广泛分布于假单胞菌属物种中。在所有检测的物种中,它是鞭毛基因表达的主要调节因子。当细胞内第二信使c-di-GMP水平较高时,它还会调节铜绿假单胞菌中参与生物膜形成的多种基因。与鞭毛基因不同,生物膜相关基因在基因组序列中并不总是容易识别。在这里,我们确定了FleQ的一个共有DNA结合序列。这使我们能够对假单胞菌菌株进行调查,并发现可能受FleQ调控且可能参与生物膜形成的新基因。