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. 2021 Jun 29;21:298. doi: 10.1186/s12870-021-03055-w

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© The Author(s) 2021

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 — Analysis of four candidate genes. a Comparison of CDS and protein sequences of four candidate genes between 9311 and CSSL128. b Comparison of expression levels of four candidate genes between 9311 and CSSL128. **Significance at p < 0.01. c Comparison of the genomic sequence of Os02g0594800 between 9311 and CSSL128. The variations between 9311 and CSSL128 are indicated in this figure. Black bars represent 5′ upstream regions and introns, light-gray bars represent 5′ and 3′ untranslated regions, dark-gray bars represent coding regions, the short dashes represent single base pair deletions