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. 2024 Apr 4;15:1372477. doi: 10.3389/fpls.2024.1372477

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Copyright © 2024 Zhao, Li, Wen, Li, Bian and Ren

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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GUS staining and activity of the target gene promoters. (A) proCHS-Bra008792; (B) proDFR-Bra027457; (C) proTT12-Bra003361; (D) proTT19-Bra008570; (E) proTT19-Bra023602; (F) proAHA10-Bra016610. Left panels: The different promoters issued from the 5′-end deletion series were fused to the 35S cauliflower mosaic virus minimal promoter upstream of the GUS reporter gene. The transient expression assays was performed in tobacco leaves. Right panels: Column diagram represent GUS activity in transformed tobacco leaves driven by the different promoters fragment. Lowercase letters indicate significant difference.