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doi: 10.15389/agrobiology.2026.3.422eng

UDC: 633.11:581.14:577.2

Acknowledgements:
Supported financially by the Russian Science Foundation, project No. 24-16-00284

 

THE USE OF GENOME-WIDE ASSOCIATION ANALYSIS TO IDENTIFY MARKERS ASSOCIATED WITH THE DURATION OF THE GROWING SEASON OF SPRING SOFT WHEAT (Triticum aestivum L.)

M.V. Solovyova , A.N. Brykova, E.V. Zuev, N.A. Shvachko

Federal Research Center Vavilov All-Russian Institute of Plant Genetic Resources, 42, ul. Bol’shaya Morskaya, St. Petersburg, 190031 Russia, e-mail maria.soloveva.97@mail.ru (✉ corresponding author), a.brykova@vir.nw.ru, e.zuev@vir.nw.ru, n.shvachko@vir.nw.ru

ORCID:
Solovyova M.V. orcid.org/0000-0002-6904-4488
Zuev E.V. orcid.org/0000-0001-9259-4384
Brykova A.N. orcid.org/0000-0002-2215-5068
Shvachko N.A. orcid.org/0000-0002-1958-5008

Final revision received September 19, 2025
Accepted February 02, 2026

Wheat (Triticum aestivum L.) is the most widely cultivated grain crop in the world, so its yield affects the global economy. Wheat breeding in the Russian Federation should be aimed not only at high adaptability, plasticity and grain quality, but also at creating early-ripening varieties with optimal growing season duration, reflecting the territorial features of the environment. Genome-Wide Association Study (GWAS) is a modern statistical method for studying the genetic foundations of important agronomic traits of plants (disease resistance, yield, stress adaptation); it allows identifying genetic loci and candidate genes associated with quantitative traits, and thereby accelerates the selection of adaptive varieties with the specified characteristics. In this work, using genome-wide association analysis (GWAS) on the VIR spring soft wheat collection, markers were identified for the first time on chromosome 5A, 2A and 6A associated with the duration of the growing season and its interphase intervals and not previously described for these signs. They are proposed as new candidates for marker-based selection (MAS) of precocity. The aim of the work was to identify genetic markers associated with the phenological characteristics of spring soft wheat using the method of genome-wide association analysis (GWAS). The material for the work was 184 samples of spring soft wheat from the collection of the All-Russian Institute of Plant Genetic Resources named after N.I. Vavilov (VIR) of various origins (92 samples from Germany, 84 from Russia, 7 from Kazakhstan, 1 from the Netherlands) and different breeding periods (local varieties, varieties before 1950 of the year, varieties of the period 1951-1991 and modern varieties). Field phenotyping was performed in 2021-2023 in the fields of the Pushkin and Pavlovsky Laboratories of the Russian Academy of Medical Sciences (Pushkin, Leningrad Region). For each sample, the duration of the sprouting-earing, earing—ripening and sprouting—ripening periods was determined. The generally accepted agricultural techniques for cultivating spring soft wheat were used in field experiments. The sample under study was genotyped at TraitGenetics GmbH (Germany) using a 20K Wheat Illumina SNP chip (www.traitgenetics.com). According to the results of genotyping, 17267 polymorphic SNPs were obtained. Subsequently, SNP filtering was performed and a final set of 13,375 polymorphic SNP markers was obtained. The population structure was determined using the STRUCTURE v 2.3.4 program. To search for associations between genotype and phenotype, the GWAS statistical method was used in the TASSEL 5.0 program using a mixed linear model (MLM+K) taking into account the kinship matrix, which reduces the proportion of false positive associations, with Bonferroni significance. Additionally, a meta-analysis was performed in the R environment, combining p-values over three years using the Fisher method. A high genetic diversity of the sample was found, the samples were divided into six groups, which mostly combined varieties from similar breeding periods (Russian varieties in two, German varieties in four). The total growing season (shoots—waxy ripeness) has lengthened from 78.7 days in 2021 to 87.1 days in 2023. According to the results of GWAS for individual years and meta-analysis, a total of 98 significant markers associated with wheat growth phases and localized in 10 chromosomes with the dominant role of chromosome 5A were identified. Some of the markers are associated with well-known wheat phenology genes (Vrn on chromosomes of the 5th homeological group, Ppd-D1 on 2D, Vrn-3/FT1 on 7A), along with which new markers have been identified. It turned out that the key role in the genetic control of the duration of the growing season is played by chromosome 5A, which has been steadily evolving for three years, which confirms the correctness of the analysis model and the quality of phenotyping.

Keywords: Triticum aestivum L., phases of plant development, phenotyping, GWAS, meta-analysis, significant markers.

 

REFERENCES

  1. Spravochnik agronoma Nechernozemnoy zoni /Pod redaktsiey G.V. Gulyaeva [Handbook of an agronomist of the Non-Chernozem zone. G.V. Gulyaev (ed.)]. Moscow, 1990 (in Russ.).
  2. International Wheat Genome Sequencing Consortium (IWGSC), Appels R., Eversole K., Stein N., Feuillet C., Keller B. et al. Shifting the limits in wheat research and breeding using a fully annotated reference genome. Science, 2018, 361(6403): eaar7191 CrossRef
  3. Masalov V.N., Berezina N.A., Chervonova I.V. Vestnik agrarnoy nauki, 2021, 2(89): 3-15 (in Russ.).
  4. Rigin B.V., Zuev E.V., Tyunin V.A., Shreyder E.R., Pizhenkova Z.S., Matvienko I.I. Trudi po prikladnoy botanike, genetike i selektsii, 2018, 179(3): 194-202 CrossRef (in Russ.).
  5. Emtseva M.V., Efremova T.T., Arbuzova V.S. Vavilovskiy zhurnal genetiki i selektsii, 2014, 16(1): 69-76 (in Russ.).
  6. Rigin B.V., Zuev E.V., Matvienko I.I., Andreeva A.S. Biotekhnologiya i selektsiya rasteniy, 2021, 4(3): 26-36 CrossRef (in Russ.).
  7. Yan L., Fu D., Li C., Blechl A., Tranquilli G., Bonafede M., Sanchez A., Valarik M., Yasuda S., Dubcovsky J. The wheat and barley vernalization gene VRN3 is an orthologue of FT. Proceedings of the National Academy of Sciences USA, 2006, 103(51): 19581-19586 CrossRef
  8. Mackay T.F.C., Stone E.A., Ayroles J.F. The genetics of quantitative traits: challenges and prospects. Nature Reviews Genetics, 2009, 10(8): 565-577 CrossRef
  9. Sehgal D., Dreisigacker S. GWAS case studies in wheat. In: Genome-Wide Association Studies. Methods in Molecular Biology, vol. 2481. F. Belzile (eds.). Humana, New York, NY, 2022: 341-351 CrossRef
  10. Liu G., Jia L., Lu L., Qin D., Zhang J., Guan P., Ni Z., Yao Y., Sun Q., Peng H. Mapping QTLs of yield-related traits using RIL population derived from common wheat and Tibetan semi-wild wheat. Theoretical and Applied Genetics, 2014, 127(11): 2415-2432 CrossRef
  11. Sukumaran S., Dreisigacker S., Lopes M., Chavez P., Reynolds M.P. Genome-wide association study for grain yield and related traits in an elite spring wheat population grown in temperate irrigated environments. Theoretical and Applied Genetics, 2015, 128(2): 353-363 CrossRef
  12. Ward B.P., Brown-Guedira G., Kolb F.L., Van Sanford D.A., Tyagi P., Sneller C.H. Genome-wide association studies for yield-related traits in soft red winter wheat grown in Virginia. PLoS ONE, 2019, 14(2): e0208217 CrossRef
  13. Shvachko N.A., Solovyova M.V., Rozanova I.V., Kibkalo I.A., Kolesova M.A., Brykova A.N., Andreeva A.S., Zuev E.V., Börner A., Khlestkina E.K. Mining of QTL for spring bread wheat spike productivity and grain quality by comparison of spring wheat varieties bred in different decades of the last century in Russia and Germany. Plants, 2024, 13(8): 1081 CrossRef
  14. Leonova I., Kiseleva A., Berezhnaya A., Orlovskaya O., Salina E. Novel genetic loci from Triticum timopheevii associated with gluten content revealed by GWAS in wheat breeding lines. International Journal of Molecular Sciences, 2023, 24(17): 13304 CrossRef
  15. Soleimani B., Lehnert H., Keilwagen J., Plieske J., Ordon F., Naseri Rad S., Perovic D. Comparison between core set selection methods using different Illumina marker platforms: a case study of assessment of diversity in wheat. Frontiers in Plant Science, 2020, 11: 1040 CrossRef
  16. Allen A.M., Winfield M.O., Burridge A.J., Downie R.C., Benbow H.R., Barker G.L.A., Wilkinson P.A., Coghill J., Waterfall C., Davassi A., Scopes G., Pirani A., Webster T., Brew F., Bloor C., Griffiths S., Bentley A.R., Alda M., Jack P., Phillips A.L., Edwards K.J. Characterisation of a wheat breeders’ array suitable for high-throughput SNP genotyping of global accessions of hexaploid bread wheat (Triticum aestivum). Plant Biotechnology Journal, 2016, 15(3): 390-401 CrossRef
  17. Pritchard J.K., Stephens M., Donnelly P. Inference of population structure using multilocus genotype data. Genetics, 2000, 155(2): 945-959 CrossRef
  18. Cinar O., Viechtbauer W. The poolr package for combining independent and dependent p values. Journal of Statistical Software, 2022, 101(1): 1-42 CrossRef
  19. Jackson D., Turner R. Power analysis for random-effects meta-analysis. Research Synthesis Methods, 2017, 8(3): 290-302 CrossRef
  20. Guo Z., Chen D., Alqudah A.M., Ganal M.W., Schnurbusch T. Genome-wide association analyses of 54 traits identified multiple loci for the determination of floret fertility in wheat. New Phytologist, 2017, 214(1): 257-270 CrossRef
  21. Zhukova I.M., Chumanova E.V., Kondrat’eva I.V., Efremova T.T. Mezhdunarodniy zhurnal prikladnikh i fundamental’nikh issledovaniy, 2021, 5: 47-51 (in Russ.).
  22. Krupnov V.A. Vavilovskiy zhurnal genetiki i selektsii, 2013, 17(3): 524-534 (in Russ.).
  23. Yan L., Loukoianov A., Tranquilli G., Helguera M., Fahima T., Dubcovsky J. Positional cloning of the wheat vernalization gene VRN1. Proceedings of the National Academy of Sciences USA, 2003, 100(10): 6263-6268 CrossRef
  24. Chen A., Dubcovsky J. Wheat TILLING mutants show that the vernalization gene VRN1 down-regulates the flowering repressor VRN2 in leaves but is not essential for flowering. PLoS Genetics, 2012, 8(12): e1003134 CrossRef
  25. Royo C., Dreisigacker S., Soriano J.M., Lopes M.S., Ammar K., Villegas D. Allelic variation at the vernalization response (Vrn-1) and photoperiod sensitivity (Ppd-1) genes and their association with the development of durum wheat landraces and modern cultivars. Frontiers in Plant Science, 2020, 11: 838 CrossRef
  26. Lv B., Nitcher R., Han X., Wang S., Ni F., Li K., Pearce S., Wu J., Dubcovsky J., Fu D. Characterization of FLOWERING LOCUS T1 (FT1) gene in Brachypodium and wheat. PLoS ONE, 2014, 9(4): e94171 CrossRef
  27. Beales J., Turner A., Griffiths S., Snape J.W., Laurie D.A. A pseudo-response regulator is misexpressed in the photoperiod insensitive Ppd-D1a mutant of wheat (Triticum aestivum L.). Theoretical and Applied Genetics, 2007, 115(5): 721-733 CrossRef
  28. Zhao Y., Wang X., Wei L., Wang J., Yin J. Characterization of Ppd-D1 alleles on the developmental traits and rhythmic expression of photoperiod genes in common wheat. Journal of Integrative Agriculture, 2016, 15(3): 502-511 CrossRef
  29. Guedira M., Xiong M., Hao Y.F., Johnson J., Harrison S., Marshall D., Brown-Guedira G. Heading date QTL in winter wheat (Triticum aestivum L.) coincide with major developmental genes VERNALIZATION1 and PHOTOPERIOD1. PLoS ONE, 2016, 11(5): e0154242 CrossRef
  30. Kiss T., Horváth Á.D., Cseh A., Berki Z., Balla K., Karsai I. Molecular genetic regulation of the vegetative-generative transition in wheat from an environmental perspective. Annals of Botany, 2024, 135(4): 605-628 CrossRef
  31. Li G., Yu M., Fang T., Cao S., Carver B.F., Yan L. Vernalization requirement duration in winter wheat is controlled by TaVRN-A1 at the protein level. The Plant Journal, 2013, 76(5): 560-571 CrossRef
  32. Yang B., Qiao L., Zheng X., Zheng J., Wu B., Li X., Zhao J. Quantitative trait loci mapping of heading date in wheat under phosphorus stress conditions. Genes, 2024, 15(9): 1150 CrossRef
  33. Gahlaut V., Jaiswal V., Balyan H.S., Joshi A.K., Gupta P.K. Multi-locus GWAS for grain weight-related traits under rain-fed conditions in common wheat (Triticum aestivum L.). Frontiers in Plant Science, 2021, 12: 758631 CrossRef
  34. Li S., Zhang C., Li J., Yan L., Wang N., Xia L. Present and future prospects for wheat improvement through genome editing and advanced technologies. Plant Communications, 2021, 2(4): 100211 CrossRef

 

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