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Detection of a novel locus involved in non-seed-shattering behaviour of Japonica rice cultivar, Oryzasativa ‘Nipponbare’

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Abstract

Key message

A novel locus, qCSS3, involved in the non-seed-shattering behaviour of Japonica rice cultivar, ‘Nipponbare’, was detected by QTL-seq analysis using the segregating population with the fixed known seed-shattering loci.

Abstract

Asian cultivated rice, Oryzasativa, was domesticated from its wild ancestor, O.rufipogon. Loss of seed shattering is one of the most recognisable traits selected during rice domestication. Three quantitative trait loci (QTLs), qSH1, qSH3, and sh4, were previously reported to be involved in the loss of seed shattering of Japonica cultivated rice, O.sativa ‘Nipponbare’. However, the introgression line (IL) carrying ‘Nipponbare’ alleles at these three loci in the genetic background of wild rice, O.rufipogon W630, showed a lower value for detaching a grain from the pedicel than ‘Nipponbare’. Here, we investigated abscission layer formation in the IL and found a partially formed abscission layer in the central region between the epidermis and vascular bundles. Based on QTL-seq analysis using the F2 population obtained from a cross between ‘Nipponbare’ and the IL, we detected two novel loci qCSS3 and qCSS9 (QTL for the Control of Seed Shattering in rice on chromosomes 3 and 9), which were found to be involved in the difference in seed-shattering degree between ‘Nipponbare’ and W630. Then, we further focused on qCSS3 in order to understand its potential role on the loss of seed shattering. The candidate region of qCSS3 was found to be located within a 526-kb region using substitution mapping analysis. Interestingly, the qCSS3 candidate region partially overlaps the selective sweep detected for Japonica but not for Indica rice cultivars, suggesting that this region harbours the mutation at a novel seed-shattering locus specifically selected for non-seed-shattering behaviour in Japonica cultivars.

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Acknowledgments

The wild rice accession, O. rufipogon W630, was provided by the National Institute of Genetics supported by the National Bioresource Project, MEXT, Japan. We thank Satoshi Natsume (Iwate Biotechnology Research Center), Kentaro Yoshida (Kobe University), Soichiro Nishiyama and Takuya Morimoto (Kyoto University) for their useful advices on our QTL-seq analysis. This study was supported in part by Grants-in-Aid from the Japan Society for the Promotion of Science (JSPS) to R.I. (Nos. 15KK0280 and 18K05594) and by the JSPS Bilateral Open Partnership Joint Research Project to R.I.

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Authors and Affiliations

Authors

Contributions

RI conceived and designed the study. YT, SS, KO, TMT, CC, and RI performed the experiments. YT, SS, KO, TI, and RI analysed the data. YT, KN, and TA contributed to bioinformatic analysis. YT, TI, and RI prepared the manuscript. All authors read and approved the final manuscript.

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Correspondence to Ryo Ishikawa.

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The authors declare that they have no conflict of interest.

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Communicated by Yunbi Xu.

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Supplemental Fig. 1

Results of the QTL-seq analysis for all chromosomes. The Δ(SNP-index) plots with statistical intervals under the null hypothesis of no QTL (orange, P < 0.01; green; P < 0.05). The red line indicates the average ΔSNP-index calculated by a sliding window analysis (PDF 822 kb)

Supplemental Fig. 2

Box plots of the BTS values of two F2 groups based on the genotypes at the candidate regions of qCSS3 and qCSS9. All F2 individuals were surveyed with five and four PCR-based molecular markers covering qCSS3 and qCSS9 regions, respectively (Supplemental Tables 1 and 2). Plants carrying the ‘Nipponbare’ (Npb) and W630 homozygous chromosomal segments for the entire candidate regions of qCSS3 and qCSS9 were selected (PDF 327 kb)

Supplemental Fig. 3

Evaluation of seed-shattering degree of the two backcross recombinant inbred lines (BRILs) carrying the W630 chromosomal segment covering the qCSS3 region in the ‘Nipponbare’ genetic background. (a) Graphical genotypes of two BRILs, BRIL42 and BRIL86. Red lines indicate the region covering qCSS3. (b) Seed-shattering degree of ‘Nipponbare’ (Npb) and the two BRILs. Data are mean ± S.D. (n = 6). ** indicates P < 0.01 by unpaired Student’s t-test (PDF 465 kb)

Supplemental Table 1

PCR-based molecular markers used in this study (PDF 79 kb)

Supplemental Table 2

Information of each 174 F2 plant used for QTL-seq analysis (PDF 98 kb)

Supplemental Table 3

Days to heading observed for F3 progeny from three F2 plants (Nos. 57, 54, and 129). Data are mean ± S.D. (n = 6) (PDF 29 kb)

Supplemental Table 4

List of the 96 genes annotated in a 526-kb candidate region of qCSS3 (PDF 36 kb)

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Tsujimura, Y., Sugiyama, S., Otsuka, K. et al. Detection of a novel locus involved in non-seed-shattering behaviour of Japonica rice cultivar, Oryzasativa ‘Nipponbare’. Theor Appl Genet 132, 2615–2623 (2019). https://doi.org/10.1007/s00122-019-03376-3

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  • DOI: https://doi.org/10.1007/s00122-019-03376-3

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