Abstract

LuxR regulators are a widely studied group of bacterial helix-turn-helix (HTH) transcription factors involved in the regulation of many genes coding for important traits at an ecological and medical level. This regulatory family is particularly known by their involvement in quorum-sensing (QS) mechanisms, i.e., in the bacterial ability to communicate through the synthesis and binding of molecular signals. However, these studies have been mainly focused on Gram-negative organisms, and the presence of LuxR regulators in the Gram-positive Actinobacteria phylum is still poorly explored. In this manuscript, the presence of LuxR regulators among Actinobacteria was assayed using a domain-based strategy. A total of 991 proteins having one LuxR domain were identified in 53 genome-sequenced actinobacterial species, of which 59% had an additional domain. In most cases (53%) this domain was REC (receiver domain), suggesting that LuxR regulators in Actinobacteria may either function as single transcription factors or as part of two-component systems. The frequency, distribution and evolutionary stability of each of these sub-families of regulators was analyzed and contextualized regarding the ecological niche occupied by each organism. The results show that the presence of extra-domains in the LuxR-regulators was likely driven by a general need to physically uncouple the signal sensing from the signal transduction. Moreover, the total frequency of LuxR regulators was shown to be dependent on genetic, metabolic and ecological variables. Finally, the functional annotation of the LuxR regulators revealed that the bacterial ecological niche has biased the specialization of these proteins. In the case of pathogens, our results suggest that LuxR regulators can be involved in virulence and are therefore promising targets for future studies in the health-related biotechnology field.

Highlights

  • The LuxR family of DNA-binding proteins is characterized by the presence of a specific regulatory helix-turn-helix (HTH)domain, named LuxR, in the C-terminal region

  • Gramnegative LuxR-type regulators involved in QS are known to be transcription factors that become activated upon sensing specific signals, usually acyl-homoserine lactones (AHLs), modulating the expression of their target genes [2,3]

  • LuxR regulators in Actinobacteria, a domain-based dual approach was applied to the complete proteomes of a set of actinobacterial organisms chosen in order to represent the diversity of Actinobacteria in terms of phylogenetic groups, morphological types, ecological niches and metabolic abilities

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Summary

Introduction

The LuxR family of DNA-binding proteins is characterized by the presence of a specific regulatory helix-turn-helix (HTH)domain, named LuxR, in the C-terminal region. The LuxR family of DNA-binding proteins is characterized by the presence of a specific regulatory helix-turn-helix (HTH). Gramnegative LuxR-type regulators involved in QS are known to be transcription factors that become activated upon sensing specific signals, usually acyl-homoserine lactones (AHLs), modulating the expression of their target genes [2,3]. These QS-related LuxR-type proteins are composed of two different modules: the N-terminal region senses and/or binds their specific QS signal, whereas the Cterminal contains a conserved HTH motif that binds DNA and promotes gene expression/repression. LuxI and its cognate luxR are frequently located in adjacent genome positions, suggesting instances of co-evolution, their distribution among bacteria is mostly discontinuous and marked by duplications, gene

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