Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-19T11:19:28.112Z Has data issue: false hasContentIssue false

Identifying QTLs for cold-induced resistance to Microdochium nivale in winter triticale

Published online by Cambridge University Press:  25 May 2011

Magdalena Szechyńska-Hebda
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland
Maria Wędzony*
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland Pedagogical University of Krakow, Podchorazych 2, Krakow 30-084, Poland
Mirosław Tyrka
Affiliation:
Rzeszow University of Technology, Wincentego Pola 2, 35-959 Rzeszów, Poland
Gabriela Gołębiowska
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland Pedagogical University of Krakow, Podchorazych 2, Krakow 30-084, Poland
Małgorzata Chrupek
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland Rzeszow University of Technology, Wincentego Pola 2, 35-959 Rzeszów, Poland
Ilona Czyczyło-Mysza
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland
Ewa Dubas
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland
Iwona Żur
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland
Elżbieta Golemiec
Affiliation:
Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, Krakow 30-239, Poland
*
*Corresponding author. E-mail: [email protected]

Abstract

Snow mould caused by Microdochium nivale (Fr.) Samuels & Hallett is the most widespread seedling disease in winter cereals. Due to the complexity of the resistance mechanisms, a poorly understood genetic background and strong interaction with winter weather conditions, it is difficult to assess the resistance of triticale cultivars via conventional inoculation methods. Genetic resistance is the most economical and environmental friendly way to control M. nivale infection; therefore, the objective of this study was to detect the quantitative trait loci (QTLs) associated with resistance components of winter triticale in a mapping population derived from a cross of the ‘Modus’ (partly resistant) and ‘SaKa 3006’ (sensitive) varieties. High-resolution mapping was conducted by using 1518 molecular markers (diversity arrays technology, simple sequence repeat and amplified fragment length polymorphism). Partial resistance components assessed in this study, i.e. candidate QTLs, were detected on chromosomes 1B, 2A, 3A, 3B, 5A, 5B, 6A, 6B and 7B, whereas QTLs describing overall seedling vitality in non-infected control plants were located on chromosomes 1B, 2B, 3A, 5A, 7B and 7R.

Type
Research Article
Copyright
Copyright © NIAB 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Börner, V, Korzun, AV, Voylokov, AJ, Worland, W and Weber, E (2000) Genetic mapping of quantitative trait loci in rye (Secale cereale L.). Euphytica 116: 203209.CrossRefGoogle Scholar
Carter, AH, Chen, XM, Garland-Campbell, K and Kidwell, KK (2009) Identifying QTL for high-temperature adult-plant resistance to stripe rust (Puccinia striiformis f. sp. tritici) in the spring wheat (Triticum aestivum L.) cultivar ‘Louise’. Theoretical and Applied Genetics 119: 11191128.CrossRefGoogle ScholarPubMed
Ergon, A, Klemsdal, S and Tronsmo, AM (1998) Interactions between cold hardening and Microdochium nivale infection on expression of pathogenesis-related genes in winter wheat. Physiological and Molecular Plant Pathology 53: 301310.CrossRefGoogle Scholar
Gołębiowska, G and Wędzony, M (2009) Cold-hardening of winter triticale ( × Triticosecale Wittm.) results in increased resistance to pink snow mould Microdochium nivale (Fr., Samuels & Hallett) and genotype-dependent chlorophyll fluorescence modulations. Acta Physiologiae Plantarum 31: 1219.CrossRefGoogle Scholar
Gonzalez, JM, Muniz, LM and Jouve, N (2005) Mapping of QTLs for androgenic response based on a molecular genetic map of (Tritocosecale Wittmack. Genome 48: 9991009.CrossRefGoogle Scholar
Hömmo, L (1996) Effect of hardening and dehardening on snow mould (Microdochium nivale) resistance. Nord Jordbruksforskning 78: 8992.Google Scholar
Hura, T, Hura, K and Grzesiak, S (2009) Physiological and biochemical parameters for identification of QTLs controlling the winter triticale drought tolerance at the seedling stage. Plant Physiology and Biochemistry 47: 210214.CrossRefGoogle ScholarPubMed
Jia, G, Chen, P, Qin, G, Bai, G, Wang, X, Wang, S, Zhou, B, Zhang, S and Liu, D (2005) QTLs for Fusarium head blight response in a wheat DH population of Wangshuibai/Alondra‘s’. Euphytica 146: 183191.CrossRefGoogle Scholar
Kuleung, C, Baenziger, PS and Dweikat, I (2004) Transferability of SSR markers among wheat, rye, and triticale. Theoretical and Applied Genetics 108: 11471150.CrossRefGoogle ScholarPubMed
Lehmensiek, A, Bovill, W, Wenzl, P, Langridge, P and Appels, R (2009) Genetic mapping in the Triticeae. Genetics and Genomics of the Triticeae, vol. 7. Heidelberg/London/New York: Springer, Dordrecht, pp. 201235.CrossRefGoogle Scholar
Nakajima, T and Abe, J (1996) Environmental factors affecting expression of resistance to pink snow mould caused by Microdochium nivale in winter wheat. Canadian Journal of Botany 74: 17831788.CrossRefGoogle Scholar
Pulli, S, Hjortesholm, K, Larsen, A, Gudleifsson, B, Larsson, S, Kristiansson, B, Hömmo, LM, Tronsmo, AM, Ruuth, P and Kristensson, K (1996) Development and Evaluation of Laboratory Testing Methods for Winter Hardiness Breeding, vol. 32. SLU, Alnarp: Nordic Gene Bank, pp. 168.Google Scholar
Reszka, E, Song, Q, Arseniuk, E, Cregan, PB and Ueng, PP (2007) The QTL controlling partial resistance to Stagonospora nodorum blotch disease in winter triticale Bogo. Plant Pathology Bulletin 16: 161167.Google Scholar
Shen, X, Francki, MG and Ohm, HW (2006) A resistance-like gene identified by EST mapping and its association with a QTL controlling Fusarium head light infection on wheat chromosome 3BS. Genome 49: 631635.CrossRefGoogle Scholar
Tronsmo, AM (1994) Effect of different cold hardening regimes on resistance to freezing on snow mould infection in timothy varieties of different origin. In: Doerffling, K, Brettschneider, B, Tantau, H and Pithan, K (eds) Crop Adaptation to Cool Climates. Brussels: European Commission (ECSP-EEC-EAEC), pp. 8389.Google Scholar
Tronsmo, AM, Hsiang, T, Okuyama, H and Nakajima, T (2001) Low temperature diseases caused by Microdochium nivale. In: Iriki, N, Gaudet, DA, Tronsmo, AM, Matsumoto, N, Yoshida, M and Nishimune, A (eds) Low Temperature Plant Microbe Interactions Under Snow. Sapporo: Hokkaido National Agricultural Experimental Station, pp. 7586.Google Scholar
Wang, Z, Wu, X, Ren, Q, Chang, X, Li, R and Jing, R (2010) QTL mapping for developmental behavior of plant height in wheat (Triticum aestivum L.). Euphytica 174: 447458.CrossRefGoogle Scholar
Wędzony, M (2003) Protocol for doubled haploid production in hexaploid Triticale ( × Triticosecale Wittm.) by crossing it with maize. In: Maluszynski, M, Kasha, KJ, Forster, BP and Szarejko, I (eds) Doubled Haploid Production in Crop Plants – A Manual. ISBN 1-4020-1544-5. Dordrecht/Boston/London: Kluwer Academic Publishers, pp. 129134.Google Scholar
Wędzony, M, Marcińska, I, Ponitka, A, Ślusarkiewicz-Jarzina, A and Wozna, J (1998) Production of doubled haploids in triticale ( × Triticosecale Wittm.) by means of crosses with maize (Zea mays L.) using Picloram and Dicamba. Plant Breeding 117: 211215.CrossRefGoogle Scholar
Zhang, K, Tian, J, Zhao, L and Wang, S (2008) Mapping QTLs with epistatic effects and QTL environment interactions for plant height using a doubled haploid population in cultivated wheat. Journal of Genetics and Genomics 35: 119127.CrossRefGoogle ScholarPubMed