A Motif Co-Occurrence Approach for Genome-Wide Prediction of Transcription-Factor-Binding Sites in Escherichia coli

Table 2.

Results of Quantitative Real-Time PCR Assays


Transcript assayed

Strain

Expression ratio
aroP ArgRpdhR clone 1 1.3 (0.33)
pdhR ArgRpdhR clone 1 2.4 (0.35)
ppa GalRytfQ clone 1 1.11 (0.45)
ytfQ GalRytfQ clone 1 1.34 (0.23)
ybdH MetJybdH clone 1 1.19 (0.21)
ybdH MetJybdH clone 2 1.55 (0.21)
ybdL MetJybdH clone 1 3.25 (0.36)
ybdL MetJybdH clone 2 3.82 (0.40)
yqeF PhoByqeG clone 1 0.208 (0.049)
yqeF PhoByqeG clone 2 0.203 (0.051)
yqeG PhoByqeG clone 1 1.35 (0.18)
yqeG PhoByqeG clone 2 1.39 (0.26)
dinJ PhoByafL clone 1 0.73 (0.16)
dinJ PhoByafL clone 2 0.85 (0.22)
dinJ PhoByafL clone 3 0.68 (0.18)
yafL PhoByafL clone 1 3.0 (0.6)
yafL PhoByafL clone 2 2.2 (0.5)
yafL PhoByafL clone 3 2.2 (0.5)
pdhR
ΔargR clone 1
1.3 (0.43)
  • Ratios resulting from mean values of triplicate assays are shown, with standard deviations given in parentheses. Ratios given are relative to wild-type MG1655 grown under the same conditions as the particular knockout strain. In the notation for naming the binding site knockouts, the name of the transcription factor whose site(s) have been mutated is followed by the name of one of the genes downstream of the mutated site(s). For example, "ArgRpdhR" indicates that at least one ArgR-binding site was knocked out upstream of the pdhR gene.

This Article

  1. Genome Res. 14: 201-208

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