4.8 Article

An atlas of the binding specificities of transcription factors in Pseudomonas aeruginosa directs prediction of novel regulators in virulence

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ELIFE
卷 10, 期 -, 页码 -

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ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.61885

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  1. National Natural Science Foundation of China [8187364, 31900443, 31870116, 32070596]
  2. Research Grants Council, University Grants Committee [21103018, 21100420, 11101619]
  3. China Postdoctoral Science Foundation [2019M663799, 2019M663794]
  4. City University of Hong Kong [9667188, 7005314, 9610424]

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High-throughput SELEX assay identified 199 unique sequence motifs describing the binding specificities of 182 TFs in Pseudomonas aeruginosa. Predicted 33,709 significant interactions between TFs and their target loci, enriched in intergenic regions. Construction of regulatory networks for virulence pathways revealed potentially significant associations of 51 TFs, 32 of which were previously uncharacterized.
A high-throughput systematic evolution of ligands by exponential enrichment assay was applied to 371 putative TFs in Pseudomonas aeruginosa, which resulted in the robust enrichment of 199 unique sequence motifs describing the binding specificities of 182 TFs. By scanning the genome, we predicted in total 33,709 significant interactions between TFs and their target loci, which were more than 11-fold enriched in the intergenic regions but depleted in the gene body regions. To further explore and delineate the physiological and pathogenic roles of TFs in P. aeruginosa, we constructed regulatory networks for nine major virulence-associated pathways and found that 51 TFs were potentially significantly associated with these virulence pathways, 32 of which had not been characterized before, and some were even involved in multiple pathways. These results will significantly facilitate future studies on transcriptional regulation in P. aeruginosa and other relevant pathogens, and accelerate to discover effective treatment and prevention strategies for the associated infectious diseases.

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