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. 2021 Jul 23;21:349. doi: 10.1186/s12870-021-03124-0

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© The Author(s) 2021

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. 4 — Heatmaps showing a selection of strongest induced and repressed DEGs in the roots of WT tomato and CCD8 RNAi line at different P starvation treatment times. A, the log2FC of the top 10 strongest P starvation-induced DEGS (at 2, 3, 4 and 5 days of P starvation) and their repression by P replenishment in WT, and DEGs at 4 days of P starvation in CCD8 RNAi line. B, the log2FC of the top 10 most repressed P starvation-induced DEGs (at 2, 3, 4 and 5 days of P starvation) and their upregulation by P replenishment in WT and CCD8 RNAi line. The heatmaps show expression profiles of the top 10 most induced/repressed P starvation DEGs; Values (in A and B) in italics represent the adjusted P-value < 0.05