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. 2021 Mar 12;12:625493. doi: 10.3389/fpls.2021.625493

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Copyright © 2021 He, Liu, Li, Lamin-Samu, Yang, Yu, Izhar, Jan, Ali and Lu.

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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Transcriptomic and qRT-PCR analysis of AtSAUR32 gene. (A) Cis-regulatory elements involved in the stimulation of AtSAUR32 used 1.5 k upstream region and analyzed by the online tool PlantCARE. (B) The tissue-specific expression levels of AtSAUR32 (Arabidopsis plants were grown under normal condition) were examined using qRT-PCR. (C) The expression pattern of AtSAUR32 under drought treatment performed by qRT-PCR analysis. (D) The expression pattern of AtSAUR32 under ABA treatment, examined by qRT-PCR. Mean values and standard deviation (+SD) are plotted as analyzed by Duncan’s multiple range (DMR) test (P < 0.05); lowercase letters (a–d) indicate significant difference.