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. 2021 Feb 11;11:3613. doi: 10.1038/s41598-021-83074-7

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© The Author(s) 2021

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 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/.

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qPCR analysis of 12 stress-responsive target genes in the flag leaf tissue (denoted with _L, highlighted in blue) and in the developing grains (denoted with _G, highlighted in orange) of DBA Artemis. The miRNA targeting the gene is shown in brackets. Relative gene expression was calculated using GAPDH as the housekeeping gene. Data are represented as the mean ± standard error (SE) (n = 3). One-way ANOVA was used to determine statistical significance across treatment groups at P < 0.05 with the l.s.d. value (least significant difference). Different letters (a–c) denote the statistical difference across the treatment groups. The treatment groups are: AtCC (DBA Artemis control group parents, progeny treated with control), AtCW (DBA Artemis control group parents, progeny treated with water-deficit stress), AtWC (DBA Artemis water-deficit stress group parents, progeny treated with control), AtWW (DBA Artemis water-deficit stress group parents, progeny treated with water-deficit stress). SRO1, poly [ADP-ribose] polymerase SRO1 gene.