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Figure 2

From: Quantitative RT-PCR analysis of differentially expressed genes in Quercus suber in response to Phytophthora cinnamomi infection

Figure 2

qRT-PCR expression profiles of six Quercus suber candidate genes, CC-NBS-LRR resistance protein ( QsRPc: a ), cinnamyl alcohol dehydrogenase2 ( QsCAD2: b ), protein disulphide isomerase ( QsPDI : c), chitinase ( QsCHI: d ), thaumatin-like protein ( QsTLP: e ), and 1,3-β-glucanase ( QsGlu: f ). Q. suber roots were infected with P. cinnamomi in a 24 h time course of gene expression. Gene expression (y-axis) was calculated as the ratio between the transcript number of the Q. suber target genes and the geometric mean of transcript copies of selected housekeeping genes [RNA polymerase II (QsRP II) and clathrin adaptor complexes medium subunit family protein (QsCACs)]. Statistically significant differences (P < 0.05) between infected and non-infected (control) plants are indicated with different letters. Error bars represent the standard deviation of four biological replicates.

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