Mapping and manipulating the Mycobacterium tuberculosis transcriptome using a transcription factor overexpression-derived regulatory network.

Publication Type:

Journal Article

Source:

Genome Biol, Volume 15, Issue 11, p.502 (2014)

Keywords:

Cloning, Molecular, Gene Expression Regulation, Bacterial, Gene Regulatory Networks, Humans, Isoniazid, Mycobacterium tuberculosis, Promoter Regions, Genetic, Regulon, Transcription Factors, Transcription, Genetic, Transcriptome, Tuberculosis

Abstract:

<p><b>BACKGROUND: </b>Mycobacterium tuberculosis senses and responds to the shifting and hostile landscape of the host. To characterize the underlying intertwined gene regulatory network governed by approximately 200 transcription factors of M. tuberculosis, we have assayed the global transcriptional consequences of overexpressing each transcription factor from an inducible promoter.</p><p><b>RESULTS: </b>We cloned and overexpressed 206 transcription factors in M. tuberculosis to identify the regulatory signature of each. We identified 9,335 regulatory consequences of overexpressing each of 183 transcription factors, providing evidence of regulation for 70% of the M. tuberculosis genome. These transcriptional signatures agree well with previously described M. tuberculosis regulons. The number of genes differentially regulated by transcription factor overexpression varied from hundreds of genes to none, with the majority of expression changes repressing basal transcription. Exploring the global transcriptional maps of transcription factor overexpressing (TFOE) strains, we predicted and validated the phenotype of a regulator that reduces susceptibility to a first line anti-tubercular drug, isoniazid. We also combined the TFOE data with an existing model of M. tuberculosis metabolism to predict the growth rates of individual TFOE strains with high fidelity.</p><p><b>CONCLUSION: </b>This work has led to a systems-level framework describing the transcriptome of a devastating bacterial pathogen, characterized the transcriptional influence of nearly all individual transcription factors in M. tuberculosis, and demonstrated the utility of this resource. These results will stimulate additional systems-level and hypothesis-driven efforts to understand M. tuberculosis adaptations that promote disease.</p>

Supplementary Files: 

TFOE Expression Data Records

Title Gene BioProject GEO Series Platform Accession Sample Method Sample Type References Release Date Repository
TFOE_1515_2175c PRJNA254351 GSE59086 GPL14824 GSM1426799 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2247_2175c PRJNA254351 GSE59086 GPL14824 GSM1426800 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5192_1830 PRJNA254351 GSE59086 GPL14824 GSM1426732 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_4908_1828
Transcriptional regulator, MerR family
PRJNA254351 GSE59086 GPL14824 GSM1426731 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_3844_1828
Transcriptional regulator, MerR family
PRJNA254351 GSE59086 GPL14824 GSM1426730 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2106_1828
Transcriptional regulator, MerR family
PRJNA254351 GSE59086 GPL14824 GSM1426729 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_9738_1830 PRJNA254351 GSE59086 GPL14824 GSM1426733 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_9820_1830 PRJNA254351 GSE59086 GPL14824 GSM1426734 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5117_1846c
Transcriptional regulator, BlaI family
PRJNA254351 GSE59086 GPL14824 GSM1426735 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_6269_1846c
Transcriptional regulator, BlaI family
PRJNA254351 GSE59086 GPL14824 GSM1426736 Tiling Array RNA 25232098 4-Jul-14 GEO