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_9476_0465c_B
\Transcriptional regulator, XRE family\\\""
PRJNA254351 GSE59086 GPL14824 GSM1426487 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_3221_0472c
\Transcriptional regulator, TetR family\\\""
PRJNA254351 GSE59086 GPL14824 GSM1426488 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5648_0472c
\Transcriptional regulator, TetR family\\\""
PRJNA254351 GSE59086 GPL14824 GSM1426489 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2579_0445c_B
RNA polymerase sigma factor RpoE
PRJNA254351 GSE59086 GPL14824 GSM1426478 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2006_0445c
RNA polymerase sigma factor RpoE
PRJNA254351 GSE59086 GPL14824 GSM1426477 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_7521_0377_C
Transcription regulator in CO-DH cluster
PRJNA254351 GSE59086 GPL14824 GSM1426476 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5061_0339c
POSSIBLE TRANSCRIPTIONAL REGULATORY PROTEIN
PRJNA254351 GSE59086 GPL14824 GSM1426466 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_5847_0339c_C
POSSIBLE TRANSCRIPTIONAL REGULATORY PROTEIN
PRJNA254351 GSE59086 GPL14824 GSM1426467 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_3770_0348_B PRJNA254351 GSE59086 GPL14824 GSM1426468 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_7445_0348_A PRJNA254351 GSE59086 GPL14824 GSM1426469 Tiling Array RNA 25232098 4-Jul-14 GEO