New levels of sophistication in the transcriptional landscape of bacteria
© BioMed Central Ltd 2009
Published: 03 August 2009
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© BioMed Central Ltd 2009
Published: 03 August 2009
An extra layer of complexity in the regulation of gene expression in bacteria is now apparent through previously unanticipated roles of noncoding and antisense RNAs.
Bacteria are the great survivors on planet Earth, where they can adapt and flourish in harsh environments ranging from deep-sea vents to acidic mine shafts. A feature of many bacteria, particularly pathogenic bacteria, is their ability to adapt and thrive in multiple environments, which provides them with a competitive advantage. For example, the facultative intracellular pathogen Listeria monocytogenes happily survives in the ambient environment as a saprophyte, but on occasions it has an inherent capacity to turn nasty and cause brain and materno-fetal infections in humans . This requires the bacterium to switch genes on and off as it traverses different environments, ranging from a saprophytic lifestyle to the gut lumen after ingestion to invasion of epithelial cells and intracellular survival. The key to the survivalist success of pathogens is their ability to coordinate, redirect and fine-tune their genetic repertoire as and when required. Traditionally, transcriptional reshaping in bacteria has been considered to be controlled by a hierarchical network of interconnected global transcriptional regulators, such as sigma factors and one- and two-component regulatory systems . In the past decade it has become apparent that the various forms of noncoding regulatory RNA (previously considered as intergenic junk) play important roles in the global regulation of cellular functions, and may represent connecting links between many cellular networks [3, 4]. As such, noncoding RNA also plays a subtle but crucial role in the coordination of the expression of bacterial virulence determinants . Two recent papers from Pascale Cossart and colleagues [6, 7] present a comprehensive microarray analysis of the trans-criptome of Listeria monocytogenes in different conditions, uncovering an unsuspected variety of regulatory roles for noncoding RNAs in controlling changes in gene expression that characterize the transition from saprophytic to pathogenic lifestyle.
Cis-encoded regulatory RNAs in principle enable a multitude of regulatory responses to stimuli, but they are mostly used for the sensing of temperature, metabolites, or metabolic stimuli (Figure 1a). They can, for example, function in translational control as ribo-switches , where the full-length mRNA is preceded by a folded 5' untranslated region (5' UTR), which can fold in different conformations depending on the stimulus, often either allowing or blocking access to the Shine-Dalgarno ribosome-binding sequence, thus controlling translation (Figure 1a). Examples are the prfA thermo-sensor of L. monocytogenes , which is involved in controlling virulence genes, or the cyclic-di-GMP-sensing riboswitch of Vibrio cholerae , which controls biofilm formation, cell differentiation, and virulence gene expression. Alternatively, the 5' UTR can form transcriptional terminator or antiterminator loops (see Figure 1a), depending on the stimulus, and as such, control transcription of the downstream gene. An example of this is in the Escherichia coli tryptophan biosynthesis operon .
A relatively newly discovered class of cis-encoded regulatory RNA is antisense RNA (Figure 1b). Antisense RNA is known to be involved in bacterial Type I toxin-antitoxin systems  and the control of incompatibility of some plasmids , but has not been implicated in controlling the expression of virulence genes. However, this may be because microarrays used in functional genomics and transcriptome studies have not incorporated probes for potential antisense transcripts. Antisense RNA shows perfect complementarity to its target sequences, and can either silence gene expression or lead to alternative processing of the mRNA.
Trans-encoded regulatory RNAs are the best-known class of noncoding RNA (Figure 1c) and represent the prokary-otic version of RNA interference . Bacterial sRNAs are anywhere between 30 and 500 nucleotides in length, but the complementary base-pairing is often restricted to a small aptamer of 8-20 nucleotides, which may have imperfect complementarity to its target mRNAs . The effects of base-pairing range from translational blocking (when bound to the 5' UTR overlapping the Shine-Dalgarno sequence) to mRNA degradation, although there are also examples where sRNA binding induces translation of the target mRNA [3, 16]. Most information on bacterial sRNA regulation has been obtained from analysis of E. coli and Salmonella enterica serovar Typhimurium, in which sRNA regulation controls many important aspects of cellular responses, ranging from outer membrane protein composition to metabolism .
While the complexity of eukaryotic transcriptional regulation is well appreciated , it was long thought that bacteria lacked many of the sophisticated regulatory mechanisms affecting the cellular transcription landscape. However, recent papers have shed new light on this subject, and have revealed that notions of the relative simplicity of bacterial gene expression severely underestimates the potential of bacteria to control expression of their genetic repertoire [6, 18–21].
Pascale Cossart and colleagues (Toledo-Arana et al. ) present one of the first comprehensive unbiased trans-criptomes of a bacterium, in this case L. monocytogenes, that includes noncoding and antisense RNAs. This tour de force reveals that gene regulatory mechanisms in bacteria are far more complex than previously appreciated. Using an unbiased, high-density tiling microarray consisting of 345,668 25-base oligonucleotide probes covering the whole genome, they have shown antisense RNAs spanning several open reading frames and long overlapping 5' and 3' UTRs, in addition to 50 sRNAs. One surprising finding was the presence of long 5' UTRs which functioned as antisense RNA, as observed upstream of the mogR gene encoding a flagellar regulatory protein . By comparing transcripts from bacteria grown in different physiological conditions (hypoxia, stationary phase, and low temperature) and from different in vivo conditions (intestinal lumen and blood), at least two of the sRNAs were found to be involved in virulence. One of these was rli38, which was upregulated 25-fold in blood and can pair to three mRNAs including that for fur, which encodes a global iron-uptake regulator. A subsequently constructed rli38 mutant was attenuated in the murine listeriosis infection model. Significantly, rli38 is absent from Listeria innocua, a nonpathogenic species closely related to L. monocytogenes. To assess transcriptional reshaping further, Toledo-Arana et al.  also investigated the transcriptomes of bacteria mutant for the global regulators PrfA (a virulence determinant regulator), SigB (an alternative sigma factor) and Hfq (an RNA chaperone). Together, these approaches identified the differential regulation of several additional RNA elements including cis-regulatory RNAs and overlapping UTRs, providing a comprehensive picture of how the transcrip-tome changes as the microorganism cycles through saprophytism and virulence. The results of the in vivo transcriptional profiling were largely verified in a study by Camejo et al.  using a L. monocytogenes macroarray.
Whereas the microarray studies described above give unique insights in the biology of L. monocytogenes (as did previous tiling microarray studies on E. coli  and Caulobacter crescentus ), we may have now started to reach the limits of what microarray and other hybridization-based techniques can tell us . Microarrays have a relatively limited dynamic range for the detection of transcript levels, owing to background, cross-hybridization, saturation and spot density and quality, and require a complete genome sequence for probe design. Also, comparison of transcription levels between independent micro-array experiments is rather challenging and mostly based on complex normalization methods . Finally, micro-array technology only measures the relative level of RNA, and does not distinguish between de novo synthesized transcripts and modified transcripts; nor does it allow accurate determination of the promoter used in the case of de novo transcription. Many of these issues can now be resolved by high-throughput sequencing of cDNA libraries .
This is illustrated in recent work by Yoder-Himes et al. , who used high-throughput sequencing to compare transcriptional patterns between two Burkholderia cenocepacia strains in conditions mimicking cystic fibrosis (CF) and soil, using strains originally isolated from a patient with CF and from soil. They also report significant changes in the transcription of noncoding RNA that are important in adaptation to external conditions. Other researchers have described transcriptomics or noncoding RNA identification using high-throughput sequencing in the bacterial pathogens Bacillus anthracis and V. cholerae [19, 20], while alternative approaches, such as immuno-precipitation of nucleic-acid-binding proteins, have been used to identify RNAs bound to the RNA chaperone Hfq in Salmonella .
Many regulatory noncoding RNAs were first described in E. coli and related Enterobacteriaceae, and depend on Hfq for their mode of action. However, with the advent of high-density microarrays and high-throughput sequencing, it is clear that paradigms based on E. coli do not necessarily hold true in other bacteria. Some bacteria lack Hfq and can be predicted to use alternative mechanisms for RNA regulation, while in many Hfq-positive bacteria the role of Hfq is still unclear . Other RNA-binding proteins, such as CsrA, may play important roles beyond their originally described functions; in the case of CsrA this is binding to Shine-Dalgarno-like sequences . All these regulatory pathways taken together allow for fine-tuning of the cellular transcriptional mechanisms, giving the bacterium the best of options to survive in adverse conditions.
It is now clear that, as in eukaryotes, bacteria exploit non-coding RNAs in their genetic regulatory repertoire, destroying another myth in the distinction between eukaryotes and prokaryotes. The development of 'next generation' DNA sequencing and direct RNA sequencing will no doubt throw even more light on the role of RNA in gene regulation [26, 27]. This will pave the way to a new era in understanding the complex and dynamic mechanisms by which bacteria adapt to the multiple environments they encounter. The next few years promise to be a voyage of discovery in terms of understanding the previously underestimated role of RNA in bacterial gene regulation.
AvV is supported by the BBSRC Institute Strategic Programme Grant to the IFR. BWW is supported by the BBSRC and The Wellcome Trust.