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. 2013 May;195(10):2424–2436. doi: 10.1128/JB.02151-12

Fig 3.

Fig 3

VttRA and VttRB influence transcription of flaA and flaD. (A) Raw RNA-seq data obtained from .wig files indicating the number of times each base was mapped for flaA and flaD in the wild-type and deletion backgrounds. (B) qRT-PCR analysis of flaA and flaD transcript levels in the wild-type and ΔvttRA and ΔvttRB strains. Mean fold change values obtained from qRT-PCR are shown adjacent to the mean fold change obtained from RNA-seq. qRT-PCR was performed four times on RNA used for RNA-seq and independently isolated RNA. Error bars represent standard deviations. *, P < 0.05 compared to the wild-type strain.