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_4853_0302_C
TetR/ACRR family transcriptional regulator
PRJNA254351 GSE59086 GPL14824 GSM1426449 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_6324_0302
TetR/ACRR family transcriptional regulator
PRJNA254351 GSE59086 GPL14824 GSM1426450 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2830_0042c
Transcriptional regulator, MarR family
PRJNA254351 GSE59086 GPL14824 GSM1426382 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2455_0042c_C
Transcriptional regulator, MarR family
PRJNA254351 GSE59086 GPL14824 GSM1426381 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_8850_0038 PRJNA254351 GSE59086 GPL14824 GSM1426380 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_8173_0038_2 PRJNA254351 GSE59086 GPL14824 GSM1426379 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_8864_0042c_B
Transcriptional regulator, MarR family
PRJNA254351 GSE59086 GPL14824 GSM1426383 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_3297_0043c
Transcriptional regulator, GntR family
PRJNA254351 GSE59086 GPL14824 GSM1426384 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5695_0043c
Transcriptional regulator, GntR family
PRJNA254351 GSE59086 GPL14824 GSM1426385 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_9257_0043c
Transcriptional regulator, GntR family
PRJNA254351 GSE59086 GPL14824 GSM1426386 Tiling Array RNA 25232098 4-Jul-14 GEO