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. 2020 Nov 11;21:784. doi: 10.1186/s12864-020-07180-y

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© The Author(s) 2020

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. 8 — qRT-PCR expression patterns of both 14 DEGs and one hub genes detected in the RNA-Seq profiles of the control and the treatment. Three biological replicates are used for qRT-PCR validation. Significant differences between means were made using One-way ANOVA followed by Tukey’s HSD post hoc test. Error bars represented standard deviations from three independent biological replicates. The asterisk (_*) stands for the levels of significant difference (*p value ≤0.05, **p value ≤0.01)