TABLE 3.
Northern blot analysis of transcript levels for selected differentially expressed genes in RNA-seq comparative analysis of RNA repair mutants and WT S. Typhimurium 14028s under MMC-induced stress
Strains and gene | Fold change by: |
|
---|---|---|
RNA-seq | Northern blotting (mean ± SD)a | |
ΔrtcR+MMC vs WT+MMC | ||
valb | 0.003 | 0.6 ± 0.06 |
gltUVWc | 0.1 | 0.7 ± 0.1 |
yafQ | 0.03 | 0.09 ± 0.01 |
dinJ | 0.03 | 0.05 ± 0.02 |
rtcA | 0.009 | NQd |
rtcB | 0.004 | NQ |
rsr | 0.003 | NQ |
rhoL | 0.3 | 0.6 ± 0.2 |
Δrsr+MMC vs WT+MMC:rhoL | 0.3 | 0.4 ± 0.1 |
ΔrtcB+MMC vs WT+MMC | ||
gltUVWc | 0.2 | 0.7 ± 0.1 |
argX | 4 | 1 ± 0.0 |
Transcript levels in each strain were normalized to the lpp transcript level, which was unchanged between strains, for calculation of the fold change between mutant and WT strains.
The Northern blot probe annealed to transcripts from valV and valW (tRNA-Val), but only valV showed a significant change in transcript levels in the comparative RNA-seq analysis of ΔrtcR+MMC versus WT+MMC.
The Northern blot probe annealed to transcripts from gltU, gltV, and gltW (tRNA-Glu); the indicated RNA-seq fold change is the average of the gltU, -V, and -W fold change values.
NQ, not quantifiable the transcript level in the mutant strain was too low to detect in quantitation, so the fold change could not be calculated.