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. 2023 Mar 9;43(3):19. doi: 10.1007/s11032-023-01365-5

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© The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

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Fig. 2 — Map-based cloning of the BnaPRS gene in DH_PR. A The average value of Δ(SNP-index) plotted along the nineteen chromosomes (X-axis) of B. napus. Signals were shown on Chromosome C06. The CIs were simulated with 10,000 times (red, p < 0.01; green, p < 0.05). B Fine mapping of the BnaPRS gene between markers I-122 and I-126 on C06. The number below chromosome refers to the number of recombinants between two markers. C Schematic diagram of predicted genes in the BnaPRS locus. The broad arrows mean predicted genes in the 284-Kb and 293-Kb intervals on C06 of NY7 and ZS11, respectively. The BnaC06G0328400ZS (BnaPAP2.C6c), BnaC06G0328700ZS (BnaPAP2.C6b), and BnaC06G0329100ZS (BnaPAP2.C6a) genes were regarded as the candidate genes (red color)