Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Transcriptional analysis of RelE family toxin overexpression in Mycobacterium tuberculosis


ABSTRACT: To understand the mechanism of action of the RelE family of toxins on metabolism of Mycobacterium tuberculosis. To this effect, toxin expression was induced under control of a tetracycline regulatable promoter and transcriptional profiles compared during overexpression of the three RelE toxin family members. Profiles were also compared to previously published profiles of drugs of known mechanism of action against this organism. For the design, RNA isolated from cells where toxin expression was induced with anhydrotetracycline was converted to Cy5-labeled cDNA whereas RNA derived from cells in which toxin expression was not induced (treated with ethanol solvent only) was converted to Cy3-labeled cDNA. Time points were taken for each overexpression condition. Treatments were performed indepedently a minimum of two times to give independent biological replicates.

ORGANISM(S): Mycobacterium tuberculosis

SUBMITTER: Helena Boshoff 

PROVIDER: E-GEOD-13998 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

The three RelE homologs of Mycobacterium tuberculosis have individual, drug-specific effects on bacterial antibiotic tolerance.

Singh Ramandeep R   Barry Clifton E CE   Boshoff Helena I M HI  

Journal of bacteriology 20100108 5


In Escherichia coli, expression of the RelE and HipA toxins in the absence of their cognate antitoxins has been associated with generating multidrug-tolerant "persisters." Here we show that unlike persisters of E. coli, persisters of Mycobacterium tuberculosis selected with one drug do not acquire cross-resistance to other classes of drugs. M. tuberculosis has three homologs of RelE arranged in operons with their apparent antitoxins. Each toxin individually arrests growth of both M. tuberculosis  ...[more]

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