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. 2019 Feb 1;6:22. doi: 10.1038/s41438-018-0098-y

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© The Author(s) 2019

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a, The interactions between SlMYB75 and eight conserved cis-elements were determined by the yeast one-hybrid assay. No auto-activation ability was detected in the eight conserved cis-elements in yeast grown on SD/ura medium containing aureobasidin A (-Ura + AbA). The interactions were determined on SD/leu medium in the presence of AbA (-Leu + AbA). b, The transcription activation ability of SlMYB75 on the promoters of several DEGs was tested using dual luciferase assays. The LUC/REN ratio of the empty vector plus the promoter was used as the calibrator (set as 1). At least six biological replicates were conducted for each combination. The values are the means ± SD. *P < 0.05; and **P < 0.01 (Student’s t-test)