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. 2022 May 3;2:12. doi: 10.1186/s43897-022-00032-1

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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. 3 — Shoot branching in CKX2-overexpressing plants is dependent on functional LS and linked to BRC1 repression. A. Representative phenotype of plants of MT, CKX2-OE#2, ls mutant and the double transgenic-mutant CKX2-OE, ls. B to E. Longitudinal shoot section of MT (B), CKX2-OE#2 (C), ls (D) and CKX2-OE, ls (E) leaf axil; bar = 2 mm. F. Expression levels of SlBRC1a and SlBRC1b in axillary buds (0.5 to 1.0 cm) harvested from the 3rd and 4th nodes of vegetative plants of MT and CKX2-OE#2. Data are means ± se of three biological samples. Statistical comparisons shown were made between the MT and transgenic line (Student’s t-test; P < 0.05)