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Maren Depke<br />

Results<br />

Pathogen Gene Expression Pr<strong>of</strong>iling<br />

<br />

stationary phase t 2<br />

<br />

stationary phase t 4<br />

exponential growth<br />

exponential growth<br />

Fig. R.5.2: Scatter plots comparing mean signal intensities <strong>of</strong> treatment groups.<br />

The signals <strong>of</strong> the three groups <strong>of</strong> “stationary phase t 2”, “stationary phase t 4”, and “exponential growth phase” were plotted after<br />

combining the three biological replicates. All sequences available on the array are shown.<br />

Table R.5.1: Results <strong>of</strong> group comparisons with statistical testing <strong>of</strong> stationary phase and exponential growth staphylococcal array<br />

data sets.<br />

number <strong>of</strong> sequences<br />

group comparison a<br />

significant with p* < 0.05 in textbook oneway<br />

ANOVA with Benjamini-Hochberg False<br />

Discovery Rate multiple testing correction<br />

absolute fold change equal<br />

to or greater than 2 AND<br />

significant with p* < 0.05<br />

stationary phase t 2 vs. exponential growth phase 2243 1423<br />

stationary phase t 4 vs. exponential growth phase 1399 1086<br />

a The 080604_SA_JH_Tiling array contains 3882 sequences <strong>of</strong> which 2825 are known transcripts. The remaining 1057 sequences were<br />

identified as new transcripts in the tiling array analysis. All sequences were included in statistical testing.<br />

Comparison <strong>of</strong> differentially regulated genes in t 2 and t 4 <strong>of</strong> stationary phase in pMEM<br />

The gene expression signatures <strong>of</strong> t 2 and t 4 stationary phase S. aureus RN1HG, which resulted<br />

from statistical comparison with the baseline <strong>of</strong> exponential growth including multiple testing<br />

correction and minimal absolute fold change cut<strong>of</strong>f 2, were compared in a Venn diagram<br />

(Fig. R.5.3 A). For 940 sequences, differential expression was observed in both time points <strong>of</strong><br />

stationary phase, while 483 and 146 sequences were specific for the t 2 and t 4 stationary phase<br />

signature, respectively.<br />

This corresponds to a fraction <strong>of</strong> 66 % <strong>of</strong> sequences regulated at t 2 , which were also<br />

differentially expressed at t 4 . Vice versa, 87 % <strong>of</strong> differentially expressed sequences at the t 4 time<br />

point were also found to be regulated at t 2 . When examining the induced and repressed<br />

sequences separately, it was first obvious that sequences regulated at both time points always<br />

possessed the same regulation direction in these two time points (Fig. R.5.3 B). Further, a slightly<br />

higher number <strong>of</strong> repressed sequences was visible in the differentially expressed sequences, but<br />

induction accounted for almost the same number <strong>of</strong> sequences as repression.<br />

In the t 2 samples, 696 sequences were induced (225 specifically for that time point), 727 were<br />

repressed (258 specifically for that time point), while in the t 4 samples 540 exhibited induction<br />

(69 specifically for that time point) and 546 exhibited repression (77 specifically for that time<br />

point). Therefore, the 940 sequences differentially expressed in both time points consisted <strong>of</strong> 471<br />

induced and 469 repressed sequences.<br />

132

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