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. 2022 Feb 4;22:62. doi: 10.1186/s12870-021-03406-7

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© The Author(s) 2022

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. 7 — Oppositely responsive transcription factor families. (a) The number and expression of transcription factors in each family that were significantly enriched (p < 0.05; indicated by an asterisk) in oppositely responsive gene-sets (up/down-regulated) in Arabidopsis, barley and/or rice. (b) The expression of all homeodomain/homeobox-leucine zipper encoding proteins that were differentially expressed in response to 3AT and/or UV treatment in in all three species. Note Arabidopsis genes annotated with an asterisk indicate genes that have an experimentally confirmed function in development, particularly root and trichome branching (ST 7c)