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. 2018 Nov 26;9:1743. doi: 10.3389/fpls.2018.01743

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Copyright © 2018 Liu, Shen, Liang, Wang, He, Zhang and Chen.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Quantitative Real-time PCR analysis of the MAwuPI transcript levels in complementary lines. At least three biological replicates and three technical replicates were performed for each data. Gene expression level was shown as fold changes, and the gene expression level in wild-type Arabidopsis plants was set as 1. Error bars represent standard error of the means of three biological repeats. Atactin is used as internal control. PI-1, pi-1 mutant; 1–8, different 35S::MAwuPI transgenic lines in Arabidopsis pi-1 mutant background.