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. 2023 Jan 6;23:11. doi: 10.1186/s12870-022-04012-x

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© The Author(s) 2023

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 12 — In vivo validation of the G1-OsLBD37-OsGA20ox1 and G1-OSH1-OsIAA15 regulation in co-transfection assays. Reporter plasmids containing the firefly luciferase (LUC) gene and renilla luciferase (REN) activities were co-transfected into rice protoplasts. The plus symbol (+) represents that the plasmid is contained in the protoplast and the minus symbol (−) represents that it is not contained. Error lines represents mean ± SD, Two-tailed Student’s t-test was performed to determine the significance of the transcription factor effects. ** represents P < 0.01. a Co-transfection assays of proOsGA20ox1:LUC and proUBI:OsLBD37. b Co-transfection assays of proOsGA20ox1:LUC, proUBI:OsLBD37 and proUBI:G1. c Co-transfection assays of proOsIAA15:LUC and proUBI:OSH1. d Co-transfection assays of Pro OsIAA15:LUC, proUBI:OSH1 and proUBI:G1