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. 2019 Mar 29;19:116. doi: 10.1186/s12870-019-1688-z

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

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Fig. 8 — GhWRKY27 activated the expression of GhCYP94C1 and GhRipen2–2 in the dual-luciferase reporter assay. a Sketch of the effecter and reporter constructs. The GhWRKY27 was cloned into the effecter vector pGreenII 62-SK. The promoters of GhCYP94C1 and GhRipen2–2 were cloned into the reporter vector pGreenII 0800-LUC. b GhWRKY27 activated the expression of GhCYP94C1. c GhWRKY27 activated the expression of GhRipen2–2. The data were indicated by the ratio of LUC to REN. The values represent the means ± SDs of six independent repeats. The significance of the data was determined using Student’s t-test (^**P < 0.01)