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. 2018 Jan 30;6:e4276. doi: 10.7717/peerj.4276

Table 1. Effect of the uptake of exogenous ldhD-siRNA by C1A germinating spores on the transcriptional level of ldhD relative to the housekeeping gene gapdh.

Treatment Final siRNA conc. (nM) Copies of ldhD relative to gapdh1,2 Fold change in transcription level (ΔΔCt) compared to untreated samples Number of biological replicates Fungal biomass yield (mg) at the time of sacrificing1
ldhD-siRNA 20 4.2E−03 ± 3E−03∗∗∗,a 0.02 4 12.3 ± 5
50 4.4E−03 ± 2E−03∗∗∗,b 0.02 5 9.3 ± 5.2
75 3.6E−04 ± 1.8E−04∗∗∗,ab 0.0017 4 15.4 ± 3.7
100 6.1E−05 ± 2.4E−05∗∗∗,ab 0.0003 4 15.9 ± 6
Untreated NA 0.21 ± 0.04 1 5 9.6 ± 2
Unrelated-siRNA 50 0.26  ±  0.07NS 1.29 2 13.5 ± 3.8

Notes.

1

Values are average ± standard deviation. Student t-test was used to test the significance of the difference of the siRNA-treated samples averages from that of the untreated sample. All ldhD-siRNA treated samples showed a significant decrease in the transcriptional level of ldhD relative to the housekeeping gene gapdh compared to the untreated control. P-value of the significant difference; ***, p-value <0.00002; **, p-value = 0.0012; NS, not significant.

2.

a,b When comparing the transcriptional level of ldhD relative to the housekeeping gene gapdh in samples treated with different concentration of ldhD-siRNA, a significant difference was observed with concentrations higher than 50 nM (p-value <0.05). Samples with the same letter were significantly different.