Oligos that had no valid expression ratios on the ten arrays were excluded from the data set for further analysis, which was carried out using the varmixt package and the VM option [50]. The resulting raw p-values were adjusted according to a Benjamini and Yekutieli procedure [51]. Genes showing a valid Erismodegib clinical trial p-value and a more than two-fold decreased or increased expression were considered buy NSC23766 as differentially expressed between

the two conditions and were retained for further study. Quantitative real time PCR Quantitative PCR experiments were performed with RNA prepared as described for microarrays. RNA aliquots were purified with the RNeasy Plus mini kit (Qiagen) to ensure the elimination of genomic DNA. Total RNA concentration was determined spectrophotometrically using a Nanodrop and RNA integrity was electrophoretically verified. Total RNA (1,9 μg) was reverse transcribed with SuperScript III first-strand synthesis system for RT-PCR (Invitrogen) using random hexamers. Real time quantitative PCR was carried out with a MyiQ single-color Real-time PCR detection system. The reaction mixture

contained 12,5 μl of MESA Blue qPCR MasterMix Plus for SYBR Assay with fluorescein (Eurogentec), 5 μl of cDNA and 300 nM of each primer in a total volume of 25 μl. Thermocycling conditions were as follow: 5 min at 95°c and 40 cycles of 15 s at 95°C, 15 s at 61°c and 1 min at 72°C. The PCR efficiency of the genes of interest and internal control genes were optimized to be similar enough by adjusting the primer concentrations to 300 nM each (data not shown). For Selleckchem PND-1186 each quantitative PCR run, non-template controls were performed to identify false positives and negative controls without reverse transcriptase were performed for each Ribonucleotide reductase cDNA synthesis reaction and verified in real time PCR to determine the presence of contaminating genomic DNA. Two biological replicates (independent cultures) and two quantitative PCR replicates were performed for each experience. Amplification products were designed to be less than 175 bp in size. The pairs of primers used

are listed in Additional file 2, Table S2. Two housekeeping genes, i.e. HEAR2922 coding for a putative RNA methyltransferase and HEAR0118 coding for a peptide deformylase, were used as standards to obtain normalized aoxB (HEAR0478) gene ratio [52] in the As(III) induced sample compared to the non-induced sample. These two housekeeping genes showed a stable expression between the two analyzed conditions (without As(III) and after an 8 hours As(III) exposure) when observing the microarrays data. The data were analyzed with the Relative Expression Software Tool [53]. Statistical significance was defined as a p-value of ≤ 0.05. 5′RACE experiment The transcriptional start site of aoxAB operon was determined using the 5′RACE system for rapid amplification of cDNA ends (Invitrogen). Total RNA was obtained as described before.