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. 2016 Mar 22;7:315. doi: 10.3389/fpls.2016.00315

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Copyright © 2016 Zhou and Li.

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) or licensor 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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Analyses of MYB-binding site of BpMYB106. (A) Analysis of the binding of BpMYB106 to the MYB2 by yeast one-hybrid (Y1H) study. Yeast cells were grown on selective dropout media: SD/-Trp-Leu/-His (TDO) with 30 mM 3-amino-1, 2, 4-triazole (3-AT). Positive control: pHIS2-p53 co-transformed with pGADT7-Rec2 vector that encodes p53 fused with GAL4 AD; negative control: pHIS2-p53 co-transformed with pGADT7-Rec2-BpMYB106. (B) Diagram of the reporter and effector vectors used in β-glucuronidase (GUS) activity analysis. (C) Analysis of the interaction between MYB2 element and BpMYB106 in tobacco leaves using GUS staining, respectively. All assays were repeated three times.