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Genetic regulation of developmental phases in winter wheat

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Abstract

The orderly development of winter wheat through its life cycle can be marked at three stages: stem elongation, heading date, and physiological maturity. The duration of a developmental phase between two stages is important in yield component generation. In this study the three developmental stages were characterized and 350 markers were mapped in a population of recombinant inbred lines (RILs) generated from a cross between two winter wheat cultivars (‘Jagger’ and ‘2174’). Three major QTLs were found to control variation in developmental process, and each of them was tightly associated with a known flowering gene, VRN-A1 on chromosome 5A, PPD-D1 on chromosome 2D, and VRN-D3 on chromosome 7D. The average contribution of the gene marker for each QTL to the total phenotypic variation (R 2) was evaluated over 3 years. The effect of VRN-A1 ranged from 21.5% at stem elongation to 17.4% at physiological maturity. The effect of PPD-D1 was minor (6.7%) at stem elongation but increased to 29.7% at heading and 20.1% at physiological maturity. The effect of VRN-D3 was not detected at stem elongation but increased to 14.6% at heading and to 20.5% at physiological maturity. Hence, the VRN-A1 locus, the PPD-D1 locus, and the VRN-D3 locus had greatest impact on development at stem elongation, heading date, and physiological maturity, respectively. Whereas the Jagger VRN-A1 and VRN-D3 alleles accelerated development, the Jagger PPD-D1 allele delayed the developmental process due to its sensitivity to photoperiod. Our findings suggest that through the appropriate combination of alleles at these three loci one would be able to regulate the various developmental phases to accommodate different agricultural needs.

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References

  • Amasino R (2004) Vernalization, competence, and the epigenetic memory of winter. Plant Cell 16:2553–2559

    Article  CAS  PubMed  Google Scholar 

  • Beales J, Turner A, Griffiths S, Snape J, Laurie D (2007) A pseudo-response regulator is misexpressed in the photoperiod insensitive Ppd-D1a mutant of wheat (Triticum aestivum L.). Theors Appl Genet 115:721–733

    Article  CAS  Google Scholar 

  • Bonnin I, Rousset M, Madur D, Sourdille P, Dupuits C, Brunel D, Goldringer T (2008) FT genome A and D polymorphisms are associated with the variation of earliness components in hexaploid wheat. Theor Appl Genet 116:383–394

    Article  CAS  PubMed  Google Scholar 

  • Chen Y, Carver BF, Wang S, Zhang F, Yan L (2009) Genetic loci associated with stem elongation and winter dormancy release in wheat. Theor Appl Genet 118:881–889

    Article  CAS  PubMed  Google Scholar 

  • Danyluk J, Kane NA, Breton G, Limin AE, Fowler DB, Sarhan F (2003) TaVRT-1, a putative transcription factor associated with vegetative to reproductive transition in cereals. Plant Physiol 132:1849–1860

    Article  CAS  PubMed  Google Scholar 

  • Dubcovsky J, Loukoianov A, Fu D, Valarik M, Sanchez A, Yan L (2006) Effect of photoperiod on the regulation of wheat vernalization genes VRN1 and VRN2. Plant Mol Biol 60:469–480

    Article  CAS  PubMed  Google Scholar 

  • Edwards JT, Carver BF, Payton ME (2007) Relationship of first hollow stem and heading in winter wheat. Crop Sci 47:2074–2077

    Article  Google Scholar 

  • Fowler DB, Breton G, Limin AE, Mahfoozi S, Sarhan F (2001) Photoperiod and temperature interactions regulate low-temperature-induced gene expression in barley. Plant Physiol 127:1676–1681

    Article  CAS  PubMed  Google Scholar 

  • Fu DL, Szucs P, Yan L, Helguer M, Skinner JS, von Zitzewitz J, Hayes PM, Dubcovsky J (2005) Large deletions within the first intron in VRN-1 are associated with spring growth habit in barley and wheat. Mol Genet Genomics 273:54–65

    Article  CAS  PubMed  Google Scholar 

  • Gonzalez FG, Slafer GA, Miralles DJ (2002) Vernalization and photoperiod responses in wheat pre-flowering reproductive phases. Field Crops Res 74:183–195

    Article  Google Scholar 

  • Gonzalez FG, Slafer GA, Miralles DJ (2003) Grain and floret number in response to photoperiod during stem elongation in fully and slightly vernalized wheats. Field Crops Res 81:17–27

    Article  Google Scholar 

  • Haun JR (1973) Visual quantification of wheat development. Agron J 65:116–119

    Article  Google Scholar 

  • Hay RKM, Ellis RP (1998) The control of flowering in wheat and barley: what recent advances in molecular genetics can reveal. Ann Bot 82:541–554

    Article  CAS  Google Scholar 

  • Hay RKM, Kirby EJM (1991) Convergence and synchrony—a review of the coordination of development in wheat. Aus J Agri Res 42:661–700

    Article  Google Scholar 

  • Košner J, Pánková K (1998) The detection of allelic variants at the recessive vrn loci of winter wheat. Euphytica 101:9–16

    Article  Google Scholar 

  • Kuchel H, Hollamby G, Langridge P, Williams K, Jefferies S (2006) Identification of genetic loci associated with ear-emergence in bread wheat. Theor Appl Genet 113:1103–1112

    Article  CAS  PubMed  Google Scholar 

  • Laurie DA, Pratchett N, Bezant JH, Snape JW (1995) RFLP mapping of five major genes and eight quantitative trait loci controlling flowering time in a winter x spring barley Hordeum vulgare (L) cross. Genome 38:575–585

    CAS  PubMed  Google Scholar 

  • Law CN, Worland AJ (1997) Genetic analysis of some flowering time and adaptive traits in wheat. New Phytol 137:19–28

    Article  Google Scholar 

  • Levy YY, Mesnage S, Mylne JS, Gendall AR, Dean C (2002) Multiple roles of Arabidopsis VRN1 in vernalization and flowering time control. Science 297:243–246

    Article  CAS  PubMed  Google Scholar 

  • McMaster GS (2009) Development of the wheat plant. In: Carver BF (ed) Wheat: science and trade. Blackwell, IA, pp 31–50

    Chapter  Google Scholar 

  • Murai K, Miyamae M, Kato H, Takumi S, Ogihara Y (2003) WAP1, a wheat APETALA1 homolog, plays a central role in the phase transition from vegetative to reproductive growth. Plant & Cell Physiol 44:1255–1265

    Article  CAS  Google Scholar 

  • Pidal B, Yan L, Fu D, Zhang F, Tranquilli G, Dubcovsky J (2009) The CArG-box in the promoter region of wheat vernalization gene VRN1 is not necessary to mediate the vernalization response. J Hered. doi:10.1093/jhered/esp002

  • Pugsley AT (1971) A genetic analysis of the spring-winter habit of growth in wheat. Aust J Agric Res 22:21–31

    Article  Google Scholar 

  • Ratcliffe OJ, Amaya I, Vincent CA, Rothstein S, Carpenter R, Coen ES, Bradley DJ (1998) A common mechanism controls the life cycle and architecture of plants. Development 125:1609–1615

    CAS  PubMed  Google Scholar 

  • Redmon LA, Krenzer EG, Bernardo DJ, Horn GW (1996) Effect of wheat morphological stage at grazing termination on economic return. Agron J 88:94–97

    Article  Google Scholar 

  • Snape JW, Butterworth K, Whitechurch E, Worland AJ (2001) Waiting for fine times: genetics of flowering time in wheat. Euphytica 119:185–190

    Article  CAS  Google Scholar 

  • Szűcs P, Skinner J, Karsai I, Cuesta-Marcos A, Haggard K, Corey A, Chen T, Hayes P (2007) Validation of the VRN-H2/VRN-H1 epistatic model in barley reveals that intron length variation in VRN-H1 may account for a continuum of vernalization sensitivity. Mol Gen Genomics 277:249–261

    Article  Google Scholar 

  • Tasma IM, Shoemaker RC (2003) Mapping flowering time gene homologs in soybean and their association with maturity (E) loci. Crop Sci 43:319–328

    Article  CAS  Google Scholar 

  • Tranquilli GE, Dubcovsky J (2000) Epistatic interactions between vernalization genes Vrn-A m 1 and Vrn-A m 2 in diploid wheat. J Hered 91:304–306

    Article  CAS  PubMed  Google Scholar 

  • Trevaskis B, Bagnall DJ, Ellis MH, Peacock WJ, Dennis ES (2003) MADS box genes control vernalization-induced flowering in cereals. Proc Natl Acad Sci USA 100:13099–13104

    Article  CAS  PubMed  Google Scholar 

  • Trevaskis B, Hemming MN, Peacock WJ, Dennis ES (2006) HvVRN2 responds to daylength, whereas HvVRN1 is regulated by vernalization and developmental status. Plant Physiol 140:1397–1405

    Article  CAS  PubMed  Google Scholar 

  • Von Zitzewitz J, Szûcs P, Dubcovsky J, Yan L, Francia E, Pecchioni N, Casas A, Chen THH, Hayes PM, Skinner JS (2005) Molecular and structural characterization of barley vernalization genes. Plant Mol Biol 59:449–467

    Article  CAS  Google Scholar 

  • Wang S, Carver BF, Yan L (2009) Genetic loci in the photoperiod pathway interactively modulate reproductive development of winter wheat. Theor App Genet 118:1339–1349

    Article  CAS  Google Scholar 

  • White JW, Herndl M, Hunt LA, Payne TS, Hoogenboom G (2008) Simulation-based analysis of effects of Vrn and Ppd loci on flowering in wheat. Crop Sci 48:678–687

    Article  Google Scholar 

  • Whitechurch EM, Slafer GA (2001) Responses to photoperiod before and after jointing in wheat substitution lines. Euphytica 118:47–51

    Article  Google Scholar 

  • Whitechurch EM, Slafer GA (2002) Contrasting Ppd alleles in wheat: effects on sensitivity to photoperiod in different phases. Field Crops Res 73:95–105

    Article  Google Scholar 

  • Yan L (2009) The wheat flowering pathway. In: Carver BF (ed) Wheat: science and trade. IA, Blackwell, pp 57–67

    Chapter  Google Scholar 

  • Yan L, Loukoianov A, Tranquilli G, Helguera M, Fahima T, Dubcovsky J (2003) Positional cloning of wheat vernalization gene VRN1. Proc Natl Acad Sci USA 100:6263–6268

    Article  CAS  PubMed  Google Scholar 

  • Yan L, Loukoianov A, Tranquilli G, Blechl A, Khan IA, Ramakrishna W, SanMiguel P, Bennetzen JL, Echenique V, Lijavetzky D, Dubcovsky J (2004) The wheat VRN2 gene is a flowering repressor down-regulated by vernalization. Science 303:1640–1644

    Article  CAS  PubMed  Google Scholar 

  • Yan L, Fu D, Li C, Blechl A, Tranquilli G, Bonafede M, Sanchez A, Valarik M, Yasuda S, Dubcovsky J (2006) From the cover: the wheat and barley vernalization gene VRN3 is an orthologue of FT. Prod Natl Acad Sci USA 103:19581–19586

    Article  CAS  Google Scholar 

  • Zadoks J, Chang T, Konzak C (1974) A decimal code for growth stages of cereals. Weed Res 14:415–421

    Article  Google Scholar 

Download references

Acknowledgments

This study was supported by the National Research Initiative of the USDA-Cooperative State Research, Education and Extension Service, grant number 2006-55606-16629 (CAP) and grant number 2007-35301-18188, the Oklahoma Center of Advanced Science and Technology (OCAST), the Oklahoma Wheat Research Foundation, and the Oklahoma Agricultural Experiment Station.

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Correspondence to Liuling Yan.

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Chen, Y., Carver, B.F., Wang, S. et al. Genetic regulation of developmental phases in winter wheat. Mol Breeding 26, 573–582 (2010). https://doi.org/10.1007/s11032-010-9392-6

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  • DOI: https://doi.org/10.1007/s11032-010-9392-6

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