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. 2023 Dec 11;24:760. doi: 10.1186/s12864-023-09849-6

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© The Author(s) 2023

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/. 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. 5 — Analysis of subcellular localization for ZmWAKL proteins and TFs. A Subcellular localization analysis conducted in N. benthamiana leaves. NLS-RFP were used as nuclear marker and show red fluorescence signals. PIP2-cherry was exclusively employed as a cell membrane marker in conjunction with ZmWAKL52-GFP co-transformation in tobacco leaves, manifesting a distinctive red fluorescent signal. Scale bar = 25 µm. B Subcellular localization examination of ZmWAKL52 in onion epidermal cells following plasmolysis. The arrow indicates GFP signals present in cell wall. Scale bar = 100 µm