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_8311_3852
POSSIBLE HISTONE-LIKE PROTEIN HNS
PRJNA254351 GSE59086 GPL14824 GSM1427052 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_6704_3852
POSSIBLE HISTONE-LIKE PROTEIN HNS
PRJNA254351 GSE59086 GPL14824 GSM1427051 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_2975_3833
Transcriptional regulator, AraC family
PRJNA254351 GSE59086 GPL14824 GSM1427041 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_4103_3833
Transcriptional regulator, AraC family
PRJNA254351 GSE59086 GPL14824 GSM1427042 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_4939_3833
Transcriptional regulator, AraC family
PRJNA254351 GSE59086 GPL14824 GSM1427043 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_1539_3840
Cell envelope-associated transcriptional attenuator LytR-CpsA-Psr, subfamily A1 (as in PMID19099556)
PRJNA254351 GSE59086 GPL14824 GSM1427044 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_4551_3840
Cell envelope-associated transcriptional attenuator LytR-CpsA-Psr, subfamily A1 (as in PMID19099556)
PRJNA254351 GSE59086 GPL14824 GSM1427045 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_7414_3840
Cell envelope-associated transcriptional attenuator LytR-CpsA-Psr, subfamily A1 (as in PMID19099556)
PRJNA254351 GSE59086 GPL14824 GSM1427046 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_3695_3849
ESX-1 secreted protein regulator EspR
PRJNA254351 GSE59086 GPL14824 GSM1427047 Tiling Array RNA 25232098 4-Jul-14 GEO
TFOE_4936_3849
ESX-1 secreted protein regulator EspR
PRJNA254351 GSE59086 GPL14824 GSM1427048 Tiling Array RNA 25232098 4-Jul-14 GEO