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. 2020 May 5;20:190. doi: 10.1186/s12870-020-02370-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. 3 — Interaction between gma-miR398c and its targets verified in transiently transformed mesophyll protoplasts. a Interaction vector [HBT-sGFP(S65T)-NOS–Targets] or [HBT-sGFP(S65T)-NOS–rTargets] inserted into mesophyll protoplasts derived from WT, OE-vector and OE-miR398c transgenic Arabidopsis plants. Bar = 50 μm; (b) Fluorescence ratio of mesophyll protoplast cells. Values are average of three replicates ± SD. Asterisks indicate significant difference applying Student’s t test (*, P < 0.05; **, P < 0.01; ***, P < 0.001). c Details regarding the gma-miR398c cleavage site in the target genes (GmCSD1a, GmCSD1b, GmCSD2a/b/c and GmCCS)