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. 2022 Dec 12;22:576. doi: 10.1186/s12870-022-03951-9

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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. 4 — The mutation of FPG on zdp/ape2 background rescues the accumulation of pri-miRNAs. RT‒qPCR detection of the relative expression levels of pri-miRNAs in Col-0, zdp-1/ape2-2, fpg-1, fpg-1/zdp-1/ape2-2, and fpg-1/zdp-1/ape2-3 plants treated with 0 ppm or 10 ppm MMS. EF1α was used as the internal control. Error bars represent standard deviation calculated from 3 independent replicates. Statistically significant differences between different genotypes are indicated by different lower-case letters (P < 0.05, one-way ANOVA per gene, performed separately)