BMC Genetics | |
Genetic variation, heritability and genotype by environment interaction of morphological traits in a tetraploid rose population | |
Frans A Krens3  Chris Maliepaard3  Richard GF Visser3  Oene Dolstra3  Kathryn Verlinden1  Carole FS Koning-Boucoiran3  Virginia W Gitonga2  | |
[1] Present address: Syngenta Seeds B.V, Enkhuizen, 1600 AA, the Netherlands;Present address: Lex + East Africa, Naivasha 20117, Kenya;Wageningen UR Plant Breeding, Wageningen University and Research Centre, Wageningen, 6700 AJ, the Netherlands | |
关键词: Genotype x environment; Correlations; Heritability; Morphological traits; Genetics; Tetraploid; Rose; | |
Others : 1088420 DOI : 10.1186/s12863-014-0146-z |
|
received in 2014-07-08, accepted in 2014-12-08, 发布年份 2014 | |
【 摘 要 】
Background
Global trade has ensured that the ornamental horticulture continues to grow worldwide, with rose hybrids being the most economically important genus (Rosa x hybrida). Due to changes in global trade and an increase in energy costs the ornamental industry has seen a shift in the production and sale of flowers from the US and Europe alone to production in Africa and Latin America. As Kenya is a major exporter of roses to Europe we studied the genetic variation and heritability of specific morphological traits in a tetraploid population grown in the Netherlands and in Kenya. The aim was to estimate genotype by environment interaction (G × E) and to investigate the implications of (G × E) for rose breeding.
Results
A tetraploid rose population (K5) from a cross between two tetraploid parents was field tested over two seasons in the Netherlands (summer and winter) and two locations in Kenya (Nairobi and Njoro). Ten traits were compared per genotype across the four environments. There were differences in trait association across the four environments showing that the traits were partially influenced by the environment.
The traits that had a low ratio of σ2ge/σ2g also showed a high value for heritability. For the traits number of petals, prickles on petioles, prickles on stems the interaction is minimal. For the traits chlorophyll content, stem width and side shoots we observed a much higher interaction ratio of 0.83, 1.43 and 3.13 respectively. The trait number of petals had the highest heritability of 0.96 and the lowest σ2ge/σ2g ratio (0.08). The trait number of side shoots (SS) with the lowest heritability (0.40) also had the highest σ2ge/σ2g ratio of 3.13.
Conclusion
Attained by this experiment showed that we have different magnitudes of non-crossover G × E interactions. For the traits number of petals, prickles on stems and prickles on petioles with a low interaction and high heritability, selection can be done at any of the environments. Thus, these traits can be confirmed at the breeding site. For the traits stem width, side shoots and chlorophyll content that had a higher interaction selection for or against these traits should be done at the production location or at least be verified there.
【 授权许可】
2014 Gitonga et al.; licensee BioMed Central.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20150119010041326.pdf | 2079KB | download | |
Figure 3. | 66KB | Image | download |
Figure 2. | 46KB | Image | download |
Figure 1. | 72KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
【 参考文献 】
- [1]FloraHolland: Facts and figures - Key figures. In: http://www.floraholland.com/en/AboutFloraHolland/Cooperative/Pages/Factsandfiguresaspx. 2012
- [2]Statistics Netherlands: Statistics on the Economy and Society of the Netherlands. Statistics Netherlands, The Hague; 2009.
- [3]Zieslin N, Mor Y: Light on roses-a review. Sci Hortic 1990, 43:1-14.
- [4]Halevy AH: Rose research - current situation and future needs. Acta Hortic 1986, 189:11-20.
- [5]De Vries DP, Dubois LAM: Rose breeding: past, present, prospects. Acta Hortic 1996, 424:241-248.
- [6]Koning-Boucoiran C, Gitonga V, Yan Z, Dolstra O, van der Linden C, van der Schoot J, Uenk G, Verlinden K, Smulders M, Krens F, Maliepaard C: The mode of inheritance in tetraploid cut roses. Theor Appl Genet 2012, 125(3):591-607.
- [7]Druitt L, Shoup M: Thornless roses. Horticulture 1991, 69:78-82.
- [8]Debener T, Mattiesch L: Construction of a genetic linkage map for roses using RAPD and AFLP markers. Theor Appl Genet 1999, 99:891-899.
- [9]Crespel L, Chirollet M, Durel CE, Zhang D, Meynet J, Gudin S: Mapping of qualitative and quantitative phenotypic traits in Rosa using AFLP markers. Theor Appl Genet 2002, 105:1207-1214.
- [10]Spiller M, Linde M, Hibrand-Saint Oyant L, Tsai C-J, Byrne D, Smulders M, Foucher F, Debener T: Towards a unified genetic map for diploid roses. Theor Appl Genet 2011, 122:489-500.
- [11]Gar O, Sargent DJ, Tsai C-J, Pleban T, Shalev G, Byrne DH, Zamir D: An autotetraploid linkage Map of rose (Rosa hybrida) validated using the strawberry (fragaria vesca) genome sequence. PLoS One 2011, 6:e20463.
- [12]Yan Z, Dolstra O, Hendriks T, Prins T, Stam P, Visser P: Vigour evaluation for genetics and breeding in rose. Euphytica 2005, 145:339-347.
- [13]GENSTAT: GenStat for Windows. 16th edition. VSN International, Hemel Hempstead, UK; 2013.
- [14]Yan W: GGEbiplot—a windows application for graphical analysis of multienvironment trial data and other types of Two-Way data. Agron J 2001, 93:1111-1118.
- [15]Yan W, Tinker NA: Biplot analysis of multi-environment trial data: Principles and applications. Can J Plant Sci 2006, 86:623-645.
- [16]De Vries DP: Juvenility in hybrid Tea-roses. Euphytica 1976, 25:321-328.
- [17]De Vries DP, Smeets L, Dubois LAM: Genetic variation for the time of first flower and shoot length in hybrid Tea-rose seedling populations under a range of temperatures. Sci Hortic 1980, 13:61-66.
- [18]Hibrand-Saint Oyant L, Crespel L, Rajapakse S, Zhang L, Foucher F: Genetic linkage maps of rose constructed with new microsatellite markers and locating QTL controlling flowering traits. Tree Genet Genomes 2008, 4:11-23.
- [19]Paterson AHDS, Hewitt JD, Zamir D, Rabinowitch HD, Lincoln SE, Lander ES, Tanksley SD: Mendelian factors underlying quantitative traits in tomato: comparison across species, generations, and environments. Genetics 1991, 127:181-197.
- [20]Moe R, Kristofferson T: The effect of temperature and light on growth and flowering of rose 'Baccara' in greenhouses. Acta Hortic 1969, 14:157-166.
- [21]Byrne TG, Doss RP, Tse ATY: Flower and shoot development in the greenhouse roses ‘Cara Mia’ and ‘Town Crier’ 333 under several temperature-photoperiodic regimes. J Am Soc Hort Sci 1978, 103:500-502.
- [22]Shin HK, Lieth JH, Kim SH: Effects of temperature on leaf area and flower size in rose. Acta Hortic 2001, 547:185-191.
- [23]Mortensen LM, Moe R: Effects of CO2 enrichment and different day/ night temperature combinations on growth and flowering of Rosa L. and Kalanchoe blossfeldiana v. poelln. Sci Hortic 1992, 51:145-153.
- [24]Rajapakse S, Byrne DH, Zhang L, Anderson N, Arumuganathan K, Ballard RE: Two genetic linkage maps of tetraploid roses. Theor Appl Genet 2001, 103:575-583.
- [25]Nobbs KJ: Breeding thornless roses. Am Rose Annual 1984, 69:37-43.
- [26]Bayse RE: A thornless rose descended from Rosa carolina. Am Rose Annual 1985, 70:82-84.
- [27]Holland JB, Nyquist WE: Cervantes-Martínez CT: Estimating and Interpreting Heritability for Plant Breeding: An Update. In Plant Breeding Reviews. John Wiley & Sons, Inc, Oxford, UK; 2010:9-112.
- [28]De Vries DP, Smeets L: Effects of temperature on growth and development of hybrid Tea-rose seedlings. Sci Hortic 1979, 11:261-268.
- [29]De Vries DP, Smeets L, Dubois LAM: Interaction of temperature and light on growth and development of hybrid tea-rose seedlings, with reference to breeding for low-energy requirements. Sci Hortic 1982, 17:377-382.