Abstract

Although transcriptional regulation is fundamental to understanding bacterial physiology, the targets of most bacterial transcription factors are not known. Comparative genomics has been used to identify likely targets of some of these transcription factors, but these predictions typically lack experimental support. Here, we used mutant fitness data, which measures the importance of each gene for a bacterium’s growth across many conditions, to test regulatory predictions from RegPrecise, a curated collection of comparative genomics predictions. Because characterized transcription factors often have correlated fitness with one of their targets (either positively or negatively), correlated fitness patterns provide support for the comparative genomics predictions. At a false discovery rate of 3%, we identified significant cofitness for at least one target of 158 TFs in 107 ortholog groups and from 24 bacteria. Thus, high-throughput genetics can be used to identify a high-confidence subset of the sequence-based regulatory predictions.

Highlights

  • Activating transcription factors (TFs)-target pairs are expected to have strong positive cofitness, where cofitness is the correlation between the fitness patterns of two genes

  • Our statistical test is stringent enough to obtain a low rate of false positives due to random correlations, false positives could arise from other sources

  • The method was applied to RegPrecise predictions and 158 TFs in 107 ortholog groups were validated with a false discovery rate of 3.0%

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Summary

Methods

We obtained known TF-target pairs in E. coli from RegulonDB version 9.1, downloaded on April 7, 2015 [19]. Version 4.0 of RegPrecise was downloaded on April 29, 2016 [13]. In RegPrecise predictions, each ortholog group has a unique regulog ID. Fitness data was obtained from http://genomics.lbl.gov/supplemental/bigfit/ and data from April 29, 2016 was used [16]. Coexpression data was obtained from the Many Microbe Microarrays Database on July 7, 2015 [21].

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