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. 2024 Dec 19;17:74. doi: 10.1186/s12284-024-00752-6

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 3 — Fine mapping of qSE1. a The qSE1 locus was initially mapped on the long arm of chromosome 1 using 135 RILs, with the dark grey region indicating its approximate interval. bqSE1 was finely mapped to a region of 246.5 kb. Six markers were used to perform genotyping of recombinants screened from 5880 F11 plants. The numbers in brackets indicated the number of recombinant crossover events occurred between flanking markers. Graphical genotypes and phenotype statistics were shown for different recombinant types. Different letters indicated significant differences at p < 0.05 (one-way analysis of variance followed by Tukey’s multiple-comparison test)