Table 2.
EV | RNAi | Ratio | |||||
---|---|---|---|---|---|---|---|
Gene | Mean | SD | Mean | SD | (RNAi/EV) | ||
Glyma03g36140 (GmNF-YA1a) | 0.21 | ± | 0.097 | 0.084 | ± | 0.048 | 0.40*** |
Glyma19g38800 (GmNF-YA1b) | 0.19 | ± | 0.099 | 0.082 | ± | 0.055 | 0.44*** |
Glyma10g10240 (putative NF-YA) | 0.021 | ± | 0.014 | 0.017 | ± | 0.015 | 0.80 |
Glyma02g35190 (putative NF-YA) | 0.036 | ± | 0.018 | 0.023 | ± | 0.015 | 0.65** |
Glyma13g08720 (phosphate transporter) | 0.026 | ± | 0.018 | 0.0098 | ± | 0.0075 | 0.38*** |
Glyma14g28780 (phosphate transporter) | 0.15 | ± | 0.10 | 0.060 | ± | 0.051 | 0.40*** |
Glyma14g36650 (phosphate transporter) | 0.0026 | ± | 0.0023 | 0.0010 | ± | 0.0006 | 0.37*** |
RiBTub1 | 0.0036 | ± | 0.0028 | 0.0014 | ± | 0.0011 | 0.40*** |
rhizogenes-transformed roots
Transcript levels of different NF-YA genes and AM-induced phosphate transporters were exemplified analyzed in chimeric plants with a Bragg wild-type background. Transcripts relative to GmSUBI-1 were determined by RT-qPCR using gene-specific primers (for primer information see Table S4 in Additional file 1). Specificity of primer pairs was assessed by sequencing of RT-qPCR products. Data are mean values + SD with n = 30 and n = 35 for EV and RNAi, respectively, coming from two independent experiments. Data of empty vector control and RNAi plants were pairwise compared by the Student's t-test. *P ≤0.05, **P ≤0.01, ***P ≤0.001. Significant changes are highlighted in bold.
EV: empty vector control; RNAi: roots expressing the RNAi construct.