Figure 1.

The induced expression of UGT85E1 and the preparation of UGT85E1 transgenic plants. (A) UGT85E1 transcript level was up-regulated by 200 mM Mannitol and 100 μM ABA treatments through reverse transcription-PCR (RT-PCR) analysis; (B) Generation and identification of UGT85E1 overexpression lines in rice. OsActin1 was used as the internal control. Error bars indicate the SD of three independent experiments. Statistically significant differences were determined by one-way ANOVA, followed by Tukey's test (P < 0.05).