Expression Patterns of OsPM1 Show Relationship to ABA Signaling Pathways. Expression Patterns of OsPM1 Show Relationship to ABA Signaling Pathways. (A)OsPM1.

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Expression Patterns of OsPM1 Show Relationship to ABA Signaling Pathways. Expression Patterns of OsPM1 Show Relationship to ABA Signaling Pathways. (A)OsPM1 was induced by drought in various organs at different developmental stages. Plants were drought stressed as described in Methods, and the indicated tissues were analyzed by RT-qPCR. SL and SR, leaves and roots from 14-d-old seedlings; FL, flag leaves; R, roots; S, stems; P, panicles. Flag leaves, roots, stems, and panicles were all from 2-month-old plants at reproductive stage. (B)OsPM1 was highly induced by ABA treatment. Six-day-old rice seedlings grown in Kimura B liquid media were subjected to various phytohormone treatments; 5 μM ABA, IAA, kinetin (KT), 2,4-D, salicylic acid (SA), jasmonic acid (JA), and gibberellic acid (GA), and 10 nM BR were added to the media for treatments, and the whole seedlings 12 h after treatments were harvested for RT-qPCR. For ethylene treatment, 1 mM ethephon solution was used for producing ethylene in a sealed container. The solvent for each phytohormone was used in mock treatments. Mock1 (water), control for indole-3-acetic acid, kinetin, and 2,4-D treatments; Mock2 (ethanol), control for ABA, salicylic acid, and jasmonic acid treatments; Mock3 (DMSO), control for BR and gibberellic acid treatments; Mock4 (water), control for ethylene treatment. (C) Temporal expression pattern of OsPM1 under ABA treatment. Fourteen-day-old seedlings grown in Kimura B liquid media were treated by ABA at a final concentration of 5 μM in the media. Leaves were harvested at the designated time points for RT-qPCR analysis. The expression at the time point 0 h was set as 1 and the relative expression levels of other time points are shown. (D) The induced expression level of OsPM1 was positively correlated with the applied ABA concentration. Leaves were harvested from the 14-d-old seedlings treated by 5, 25, or 50 μM ABA in the media for different time periods and then subjected to RT-qPCR analysis. The expression level at time point “0 h” was set as 1 and the relative expression levels of other time points are shown. In (A) to (D), data are shown as means ± sd, and three independent samples each pooled from three individual plants were used for assay. One-way ANOVA was performed for (A) and (C). Different letters indicate significant differences (P < 0.05). Student’s t test was performed for the significance of difference between treatment and the corresponding mock experiment in (B). Two-way ANOVA followed by Bonferroni’s post-hoc test was performed for (D). Different letters with the same superscript indicate significant differences (P < 0.05) between different time points treated by the same concentration of ABA. **P < 0.01 indicates significant differences between samples treated by different concentrations of ABA at the same time points (Supplemental Data Set 2). Lingya Yao et al. Plant Cell 2018;30:1258-1276 ©2018 by American Society of Plant Biologists