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. 2019 Jan 30;9:932. doi: 10.1038/s41598-018-37039-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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(a) qRT-PCR of selective up-regulated genes under 1 M salt treatment in P. odorifer (Legend:- AS: Asparagine synthetase, NAC: NAC TF, WRKY71: WRKY TF 71, TPP: Trehalose phosphate phosphatase, GDH: Glutamate dehydrogenase, ERF4: Ethylene responsive factor 4, SPDS: Spermidine synthase, NHX1: Na +/H + antiporter 1, GS: Glutamine synthetase, ALDH: Aldehyde dehydrogenase, SOS2: Salt overly sensitive-2, P5CS: 1-pyrroline 5 carboxylate synthase, GAD: glutamate decarboxylase, SSADH: Succinic semialdehyde dehydrogenase, BADH2: Betaine aldehyde dehydrogenase 2). (b) Scatter plot depicting the correlation between the RNAseq and qRT-PCR data. The figure shows expression changes (log2 fold) measured by RNAseq and qRT-PCR analyses of the selected genes. A linear trend line is shown.