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. 2016 Jul 25;7:1082. doi: 10.3389/fpls.2016.01082

FIGURE 1.

FIGURE 1

Growth characteristics of GmCLC1-transgenic Arabidopsis thaliana. (A) Genotyping by PCR of GmCLC1-transgenic A. thaliana lines (L1–L5) to confirm success in transformation. All five lines contain the transgene. Comparison in (B) seed germination rate, (C) seedlings growth, and (D) root lengths between A. thaliana wild-type (WT) and transgenic plants (GmCLC1; using L1 as the representative) sown on MS agar medium containing different concentrations of NaCl. (B) Seeds of WT and GmCLC1 (30 seeds per plate each with three replicates) were surface-sterilized and stratified at 4°C for 2–4 days and then sown on MS medium supplemented with 150 or 200 mM NaCl. After 7 days of incubation, the seed germination rate (%) was measured. (C,D) 5-days-old WT and GmCLC1 with nearly equal root lengths were transferred to MS agar medium supplemented with 0, 150, or 200 mM NaCl. After 5 days of vertical incubation, the seedlings’ growth phenotypes were photographed and the root lengths measured. M: DNA markers. /∗∗: The difference between WT and GmCLC1 was significant at p < 0.05 and p < 0.01 respectively, using Duncan’s test. Each bar represents the mean and SD of for (C) 30 seeds per plate each with three replicates; for (D) more than 10 plants for each treatment.