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. 2016 Jul 20;67(17):5217–5232. doi: 10.1093/jxb/erw288

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© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 8. — Real-time quantitative RT-PCR analyses to determine transcript levels of auxin- and JA-related genes after 12- and 24-h DEX treatments. The PES (#28), BOP1 (#7), and WDR12 (#8) RNAi seedlings (7 DAS) grown in liquid culture were treated with ethanol (–) or 20 µM DEX (+) for 12h or 24h. The first leaves were collected for the analyses. Transcript levels were quantified relative to (–)DEX samples using UBC10 mRNA levels as a control. Each value represents the mean ±SD of three replicates per experiment. *, P≤0.05; **, P≤0.01. (A) Auxin-related genes after 12-h DEX treatment. (B) Auxin-related genes after 24-h DEX treatment. (C) JA-related genes after 12-h DEX treatment. (D) JA-related genes after 24-h DEX treatment. (This figure is available in colour at JXB online.)