Abstract

BackgroundThe genome of Mycobacterium tuberculosis harbors four copies of a cluster of genes termed mce operons. Despite extensive research that has demonstrated the importance of these operons on infection outcome, their physiological function remains obscure. Expanding databases of complete microbial genome sequences facilitate a comparative genomic approach that can provide valuable insight into the role of uncharacterized proteins.ResultsThe M. tuberculosis mce loci each include two yrbE and six mce genes, which have homology to ABC transporter permeases and substrate-binding proteins, respectively. Operons with an identical structure were identified in all Mycobacterium species examined, as well as in five other Actinomycetales genera. Some of the Actinomycetales mce operons include an mkl gene, which encodes an ATPase resembling those of ABC uptake transporters. The phylogenetic profile of Mkl orthologs exactly matched that of the Mce and YrbE proteins. Through topology and motif analyses of YrbE homologs, we identified a region within the penultimate cytoplasmic loop that may serve as the site of interaction with the putative cognate Mkl ATPase. Homologs of the exported proteins encoded adjacent to the M. tuberculosis mce operons were detected in a conserved chromosomal location downstream of the majority of Actinomycetales operons. Operons containing linked mkl, yrbE and mce genes, resembling the classic organization of an ABC importer, were found to be common in Gram-negative bacteria and appear to be associated with changes in properties of the cell surface.ConclusionEvidence presented suggests that the mce operons of Actinomycetales species and related operons in Gram-negative bacteria encode a subfamily of ABC uptake transporters with a possible role in remodeling the cell envelope.

Highlights

  • The genome of Mycobacterium tuberculosis harbors four copies of a cluster of genes termed mce operons

  • The M. tuberculosis H37Rv genome encodes 24 Mce proteins, each of which contains a conserved domain of 304 amino acids defined by the TIGRFAM family: TIGR00996 (IPR005693)

  • The mce genes in M. tuberculosis are clustered in groups of six; each cluster is preceded by two copies of a gene termed yrbE (Figure 1)

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Summary

Introduction

The genome of Mycobacterium tuberculosis harbors four copies of a cluster of genes termed mce operons. A putative Mycobacterium tuberculosis virulence gene, named mce1A, was originally identified because its expression in Escherichia coli enabled this noninvasive bacterium to enter mammalian epithelial cells [1]. Sequencing of the M. tuberculosis genome revealed that mce1A (Rv0169) was part of an operon that encoded eight putative membraneassociated proteins: YrbEA-B, MceA-F [2,3]. This operon is present four times in the M. tuberculosis genome (mce). YrbE1A yrbE1B mce1A mce1B mce1C 0172 mce1D 0173 mce1E. 0586 0587 0588 0589 0590 mce2R yrbE2A yrbE2B mce2A mce2B 0591 mce2C 0592 mce2D Continued interest in the function of the M. tuberculosis mce operons stems from reports of the profound effect of disruption of mce operons on growth and virulence of the (page number not for citation purposes)

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