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Unraveling yield-related traits with QTL analysis and dissection of QTL × environment interaction using a high-density bin map in rapeseed (Brassica napus. L)

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Abstract

According to the temperature and duration of the vernalization stage, three types of varieties adapted to different environments were bred in rapeseed breeding: spring, semi-winter, and winter type. Usually in a particular rapeseed producing area, only one type (spring or winter) is cultivated and almost none of the rapeseed varieties can adapt to both environments, which is mainly caused by the strong G × E, but how G × E affected yield-related traits is still unclear in rapeseed. In the present study, we tried to perform QTL mapping and dissect G × E into QTL × environments interactions (QTL × E) for seven yield traits in a DH population derived from No.2127 (a spring DH line) × ZY821 (a semi-winter cultivar) using a high-density SNP bin map. We described the impact of QTL × E on the genetic control of yield traits. Firstly, for the same trait of the same DH line, significant phenotypic difference for all the seven traits were observed when grown in the spring and semi-winter environment, respectively. Secondly, for five out of seven traits, the broad-sense heritability in the spring (adaptive) environment was higher over the semi-winter (stress) environment. Thirdly, total 74 non-redundant QTL including 26 consensus QTL and 48 trial-specific ones were detected, the positive additive effects of QTL were dispersed in both parents for all the seven traits. Among the 26 consensus QTL, eleven were specific to the spring or semi-winter environment, and the other 15 were common between the two environments, including four for flowering time (FT), and four for silique length (SL), 3 for thousand seed weight (TSW), each of them explained 6.4–26.1% of the phenotypic variation. Our results revealed that QTL × E for the seven yield-related traits mainly reflected by the environment-specific QTL, partly reflected by the same QTL with different expressions. These findings provided a better understanding of the genetic basis of QTL × E affected yield-related traits in rapeseed.

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References

  • Arcade A, Labourdette A, Falque M, Mangin B, Chardon F, Charcosset A, Joets J (2004) BioMercator: integrating genetic maps and QTL towards discovery of candidate genes. Bioinformatics 20:2324

    Article  CAS  Google Scholar 

  • Beavis W, Keim P (1996) Identification of quantitative trait loci that are affected by environment. Genotype-by-environment interaction CRC Press, Boca Raton, pp 123–149

    Google Scholar 

  • Blum A, Jordan WR (1985) Breeding crop varieties for stress environments. Crit Rev Plant Sci 2:199–238

    Article  Google Scholar 

  • Ceccarelli S (1989) Wide adaptation. How wide? Euphytica 40:197–205

    Google Scholar 

  • Chalhoub B, Denoeud F, Liu S et al (2014) Early allopolyploid evolution in the post-Neolithic Brassica napus oilseed genome. Science 345:950–953

    Article  CAS  Google Scholar 

  • Chen BY, Heneen WK, Jönsson R (1988) Resynthesis of Brassies napus L. through interspecific hybridization between B. alboglabra Bailey and B. campestris L. with special emphasis on seed colour. Plant Breed 101:52–59

    Article  Google Scholar 

  • Chen W, Zhang Y, Liu X, Chen B, Tu J, Fu T (2007) Detection of QTL for six yield-related traits in oilseed rape (Brassica napus) using DH and immortalized F2 populations. Theor Appl Genet 115:849–858

    Article  CAS  Google Scholar 

  • Chen G, Geng J, Rahman M, Liu X, Tu J, Fu T, Li G, McVetty PBE, Tahir M (2010) Identification of QTL for oil content, seed yield, and flowering time in oilseed rape (Brassica napus). Euphytica 175:161–174

    Article  CAS  Google Scholar 

  • Chen X, Li X, Zhang B, Xu J, Wu Z, Wang B, Li H, Younas M, Huang L, Luo Y, Wu J, Hu S, Liu K (2013) Detection and genotyping of restriction fragment associated polymorphisms in polyploid crops with a pseudo-reference sequence: a case study in allotetraploid Brassica napus. BMC Genom 14:346–357

    Article  Google Scholar 

  • Emebiri L, Moody D (2006) Heritable basis for some genotype–environment stability statistics: inferences from QTL analysis of heading date in two-rowed barley. Field crops research 96:243–251

    Article  Google Scholar 

  • Fan C, Cai G, Qin J, Li Q, Yang M, Wu J, Fu T, Liu K, Zhou Y (2010) Mapping of quantitative trait loci and development of allele-specific markers for seed weight in Brassica napus. Theor Appl Genet 121:1289–1301

    Article  CAS  Google Scholar 

  • Goffinet B, Gerber S (2000) Quantitative trait loci: a meta-analysis. Genetics 155:463–473

    CAS  PubMed  PubMed Central  Google Scholar 

  • He Y, Wu D, Wei D, Fu Y, Cui Y, Dong H, Tan C, Qian W (2017) GWAS, QTL mapping and gene expression analyses in Brassica napus reveal genetic control of branching morphogenesis. Sci Rep 7:15971–15980

    Article  Google Scholar 

  • Li Z, Luo L, Mei H, Wang D, Shu Q, Tabien R, Zhong D, Ying C, Stansel J, Khush G (2001) Overdominant epistatic loci are the primary genetic basis of inbreeding depression and heterosis in rice. I. Biomass and grain yield. Genetics 158:1737–1753

    CAS  PubMed  PubMed Central  Google Scholar 

  • Li Z, Yu S, Lafitte H, Huang N, Courtois B, Hittalmani S, Vijayakumar C, Liu G, Wang G, Shashidhar H (2003) QTL × environment interactions in rice. I. Heading date and plant height. Theor Appl Genet 108:141–153

    Article  CAS  Google Scholar 

  • Li D, Wang X, Zhang X, Chen Q, Xu G, Xu D et al (2016) The genetic architecture of leaf number and its genetic relationship to flowering time in maize. New Phytol 210(1):256–268

    Article  CAS  Google Scholar 

  • Li N, Song D, Peng W, Zhan J, Shi J, Wang X, Liu G, Wang H (2019) Maternal control of seed weight in rapeseed (Brassica napus L.): the causal link between the size of pod (mother, source) and seed (offspring, sink). Plant Biotechnol J 17:736–749

    Article  CAS  Google Scholar 

  • Li B, Gao J, Chen J, Wang Z, Shen W, Yi B, Wen J, Ma C, Shen J, Fu T, Tu J (2020) Identification and fine mapping of a major locus controlling branching in Brassica napus. Theor Appl Genet 133:771–783

    Article  CAS  Google Scholar 

  • Liu H (1984) The genetics and breeding of rapeseed. Shanghai Science and Technology Press

  • Long Y, Shi J, Qiu D, Li R, Zhang C, Wang J, Hou J, Zhao J, Shi L, Park BS (2007) Flowering time quantitative trait loci analysis of oilseed Brassica in multiple environments and genomewide alignment with Arabidopsis. Genetics 177:2433–2444

    Article  CAS  Google Scholar 

  • Mei D, Wang H, Hu Q, Li Y, Xu Y, Li Y (2009) QTL analysis on plant height and flowering time in Brassica napus. Plant Breed 128:458–465

    Article  Google Scholar 

  • Messmer R, Fracheboud Y, Banziger M, Vargas M, Stamp P, Ribaut JM (2009) Drought stress and tropical maize: QTL-by-enviroment interactions and stability of QTLs across environments for yield components and secondary traits. Theor Appl Genet 119:913–930

    Article  Google Scholar 

  • Parent B, Bonneau J, Maphosa L, Kovalchuk A, Langridge P, Fleury D (2017) Quantifying wheat sensitivities to environmental constraints to dissect genotype × environment interactions in the field. Plant Physiol 174:1669–1682

    Article  CAS  Google Scholar 

  • Paterson A, Saranga Y, Menz M, Jiang CX, Wright R (2003) QTL analysis of genotype × environment interactions affecting cotton fiber quality. Theor Appl Genet 106:384–396

    Article  CAS  Google Scholar 

  • Quijada PA, Udall JA, Lambert B, Osborn TC (2006) Quantitative trait analysis of seed yield and other complex traits in hybrid spring rapeseed (Brassica napus L.): 1. Identification of genomic regions from winter germplasm. Theor Appl Genet 113:549–561

    Article  CAS  Google Scholar 

  • SAS Institute (1999) SAS/STAT user’s guide, version 8. SAS Institute, Cary

  • Sari-Gorla M, Calinski T, Kaczmarek Z, Krajewski P (1997) Detection of QTL × environment interaction in maize by a least squares interval mapping method. Heredity 78:146–157

    Google Scholar 

  • Shi J, Li R, Qiu D, Jiang C, Long Y, Morgan C, Bancroft I, Zhao J, Meng J (2009) Unraveling the complex trait of crop yield with quantitative trait loci mapping in Brassica napus. Genetics 182:851

    Article  CAS  Google Scholar 

  • Shi J, Zhan J, Yang Y, Ye J, Huang S, Li R, Wang X, Liu G, Wang H (2015) Linkage and regional association analysis reveal two new tightly-linked major-QTLs for pod number and seed number per pod in rapeseed (Brassica napus L.). Sci Rep 5:14481–14490

    Article  CAS  Google Scholar 

  • Tanger P, Klassen S, Mojica JP, Lovell JT, Moyers BT, Baraoidan M et al (2017) Field-based high throughput phenotyping rapidly identifies genomic regions controlling yield components in rice. Sci Rep 7:42839

    Article  CAS  Google Scholar 

  • Tudor E, Jones M, He Z, Bancroft I, Trick M, Wells R, Irwin J, Dean C (2020) QTL-seq identifies BnaFT.A02 and BnaFLC.A02 as candidates for variation in vernalization requirement and response in winter oilseed rape (Brassica napus). Plant Biotechnol J. doi:https://doi.org/10.1111/pbi.13421

    Article  PubMed  Google Scholar 

  • Udall JA, Quijada PA, Lambert B, Osborn TC (2006) Quantitative trait analysis of seed yield and other complex traits in hybrid spring rapeseed (Brassica napus L.): 2. Identification of alleles from unadapted germplasm. Theor Appl Genet 113:597–609

    Article  CAS  Google Scholar 

  • Wang S, Basten C, Zeng Z (2007) Windows QTL cartographer 2.5. Department of Statistics, North Carolina State University, Raleigh

    Google Scholar 

  • Wang X, Chen L, Wang A, Wang H, Tian J, Zhao X, Chao H, Zhao Y, Zhao W, Xiang J, Gan J, Li M (2016) Quantitative trait loci analysis and genome-wide comparison for silique related traits in Brassica napus. BMC Plant Biol 16:71–80

    Article  CAS  Google Scholar 

  • Wang H, Zaman QU, Huang W, Mei D, Liu J, Wang W, Ding B, Hao M, Fu L, Cheng H, Hu Q (2019) QTL and candidate gene identification for silique length based on high-dense genetic map in Brassica napus L. Front Plant Sci 10:1579–1591

    Article  Google Scholar 

  • Wang H, Yan M, Xiong M, Wang P, Liu Y, Xin Q, Wan L, Yang G, Hong D (2020a) Genetic dissection of thousand-seed weight and fine mapping of cqSW.A03-2 via linkage and association analysis in rapeseed (Brassica napus L.). Theor Appl Genet 133:1321–1335

    Article  CAS  Google Scholar 

  • Wang T, Wei L, Wang J, Lu k, Li J, Timko M, Liu l (2020b) Integrating GWAS, linkage mapping and gene expression analyses reveals the genetic control of growth period traits in rapeseed (Brassica napus L.). Biotechnol Biofuels. https://doi.org/10.1186/s13068-020-01774-0

    Article  PubMed  PubMed Central  Google Scholar 

  • Yang P, Shu C, Chen L, Xu J, Wu J, Liu K (2012) Identification of a major QTL for silique length and seed weight in oilseed rape (Brassica napus L.). Theor Appl Genet l25:285–296

    Article  Google Scholar 

  • Yang Y, Shen Y, Li S, Ge X, Li Z (2017) High Density Linkage Map Construction and QTL Detection for three silique-related traits in Orychophragmus violaceus derived Brassica napus population. Front Plant Sci 8:1512

    Article  Google Scholar 

  • Yin Y, Wang H, Liao X (2009) Analysis of the development of rapeseed industry in China in 2009. Chin J Oil Crop Sci 31:259–262

    Google Scholar 

  • Yu H, Xie W, Wang J, Xing Y, Xu C, Li X, Xiao J, Zhang Q (2011) Gains in QTL detection using an ultra-high density SNP map based on population sequencing relative to traditional RFLP/SSR markers. PloS ONE 6:e17595

    Article  CAS  Google Scholar 

  • Zhang L, Yang G, Liu P, Hong D, Li S, He Q (2011) Genetic and correlation analysis of silique-traits in Brassica napus L. by quantitative trait locus mapping. Theor Appl Genet 122:1–11

Download references

Acknowledgements

This research was funded by the National Key Research and Development Program of China (2017YFD0101700), the National Natural Science Foundation of China (31301361, 31171589).

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YX, JX drafted manuscript and conducted experiment, XZ revised the manuscript, YX, JX, GT LX carried out analysis, BX provide reagents for experiments, YX GT collected phenotypic data, KL supervised the study.

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Correspondence to Jinsong Xu.

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Electronic supplementary material

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10681_2020_2708_MOESM1_ESM.xls

Supplemental table 1 (a): ANOVA for six yield-related traits in the spring environment. (b) ANOVA for seven yield-related traits in the semi-winter environment. (XLSX 20 kb)

10681_2020_2708_MOESM2_ESM.xls

Supplemental table 2 (a): Phenotypic correlation coefficients among traits for DH population in the two trials in the spring environment. (b) Phenotypic correlation coefficients among traits for DH population in the two trials in the semi-winter environment. (XLSX 19 kb)

10681_2020_2708_MOESM3_ESM.xls

Supplemental table 3 (a): The list of 108 original QTL identified in the four individual trials. (b) The list of the 57 unique-QTL obtained after meta-analysis of the 74 non-redundant QTL. (XLSX 73 kb)

10681_2020_2708_MOESM4_ESM.ppt

Supplemental figure 1: The main climate factors in the rapeseed growing period in 4 trails. (A1-A4) The changes of climatic factors, calculated monthly, in the two semi-winter microenvironments. Fine lines with different colors represent the different microenvironments. (B1-B4) The changes of climatic factors, calculated monthly, in the two spring microenvironments. Fine lines with different colors represent the different microenvironments. (PPT 270 kb)

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Xie, Y., Xu, J., Tian, G. et al. Unraveling yield-related traits with QTL analysis and dissection of QTL × environment interaction using a high-density bin map in rapeseed (Brassica napus. L). Euphytica 216, 171 (2020). https://doi.org/10.1007/s10681-020-02708-5

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