Abstract

Bacterial promoters are usually formed by multiple cis-regulatory elements recognized by a plethora of transcriptional factors (TFs). From those, global regulators are key elements since these TFs are responsible for the regulation of hundreds of genes in the bacterial genome. For instance, Fis and IHF are global regulators that play a major role in gene expression control in Escherichia coli, and usually, multiple cis-regulatory elements for these proteins are present at target promoters. Here, we investigated the relationship between the architecture of the cis-regulatory elements for Fis and IHF in E. coli. For this, we analyze 42 synthetic promoter variants harboring consensus cis-elements for Fis and IHF at different distances from the core −35/−10 region and in various numbers and combinations. We first demonstrated that although Fis preferentially recognizes its consensus cis-element, it can also recognize, to some extent, the consensus-binding site for IHF, and the same was true for IHF, which was also able to recognize Fis binding sites. However, changing the arrangement of the cis-elements (i.e., the position or number of sites) can completely abolish the non-specific binding of both TFs. More remarkably, we demonstrated that combining cis-elements for both TFs could result in Fis and IHF repressed or activated promoters depending on the final architecture of the promoters in an unpredictable way. Taken together, the data presented here demonstrate how small changes in the architecture of bacterial promoters could result in drastic changes in the final regulatory logic of the system, with important implications for the understanding of natural complex promoters in bacteria and their engineering for novel applications.

Highlights

  • Bacteria have evolved complex gene regulatory networks to coordinate the expression level of each gene in response to changing environmental conditions

  • In order to investigate the effect of promoter architecture in the regulation by Fis and IHF, we evaluated the effect of 12 complex promoters constructed in early work (Monteiro et al, 2018) and we constructed 30 new combinatorial promoters with consensus DNA sequences for Fis (Fis-BS) and IHF (IHF-BS) binding sites positioned upstream of a weak core promoter (−35/−10 region) at specific positions (1–4) centered at the −61, −81, −101, and −121 regions related to the transcriptional start site (TSS) (Figure 1)

  • Bacteria are naturally endowed with complex promoters harboring multiple binding sites for several transcriptional factors (TFs)

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Summary

Introduction

Bacteria have evolved complex gene regulatory networks to coordinate the expression level of each gene in response to changing environmental conditions In this aspect, a typical bacterium such as Escherichia coli uses around 300 different transcriptional factors (TFs) to control the expression of more than 5,000 genes, and gene regulation in bacteria has been extensively investigated in the last six decades (Lozada-Chavez, 2006). Many cis-regulatory elements for many TFs from E. coli have been experimentally characterized, mapped, and compiled in databases such as RegulonDB and EcoCyc (GamaCastro et al, 2016; Keseler et al, 2017) Analysis of these datasets demonstrates that TFs usually act in a combinatorial way to control gene expression, where multiple cis-regulatory elements for different TFs are located in the upstream region of the target genes (Guazzaroni and Silva-Rocha, 2014; Rydenfelt et al, 2014; Gama-Castro et al, 2016). The arrangement of cis-regulatory elements at the target promoters is crucial to determine which TFs will be able to control the target gene and how these regulators interact with each other once bound to the DNA (Collado-Vides et al, 1991; Ishihama, 2010)

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