Abstract
Key message
Commercial heterosis for grain yield is present in hybrid wheat but long-term competiveness of hybrid versus line breeding depends on the development of heterotic groups to improve hybrid prediction.
Abstract
Detailed knowledge of the amount of heterosis and quantitative genetic parameters are of paramount importance to assess the potential of hybrid breeding. Our objectives were to (1) examine the extent of midparent, better-parent and commercial heterosis in a vast population of 1,604 wheat (Triticum aestivum L.) hybrids and their parental elite inbred lines and (2) discuss the consequences of relevant quantitative parameters for the design of hybrid wheat breeding programs. Fifteen male lines were crossed in a factorial mating design with 120 female lines, resulting in 1,604 of the 1,800 potential single-cross hybrid combinations. The hybrids, their parents, and ten commercial wheat varieties were evaluated in multi-location field experiments for grain yield, plant height, heading time and susceptibility to frost, lodging, septoria tritici blotch, yellow rust, leaf rust, and powdery mildew at up to five locations. We observed that hybrids were superior to the mean of their parents for grain yield (10.7 %) and susceptibility to frost (−7.2 %), leaf rust (−8.4 %) and septoria tritici blotch (−9.3 %). Moreover, 69 hybrids significantly (P < 0.05) outyielded the best commercial inbred line variety underlining the potential of hybrid wheat breeding. The estimated quantitative genetic parameters suggest that the establishment of reciprocal recurrent selection programs is pivotal for a successful long-term hybrid wheat breeding.
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Acknowledgments
M. Gowda, J. Mühleisen and Y. Zhao were supported by BMBF within the HYWHEAT project (Grant ID: FKZ0315945D).
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The authors declare that they have no conflict of interest.
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Communicated by P. Langridge.
C. F. H. Longin and M. Gowda contributed equally to this work.
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Supplementary Figure S1: Efficiency of reducing specific combining ability effects by increasing the number of different gametes in a tester for fT1T2 = 0 (O), fT1T2 = 0.25 (Δ), fT1T2 = 0.5 (+). Number of gametes = 2 means either 2 inbred testers or 1 single cross, tester lines = 4 means either 4 inbreds, or 2 single crosses, or 1 double cross tester and so on.(EPS 435 kb)
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Supplementary Figure S2: Association between performance of the 1604 wheat hybrids and the hybrid performance predicted based on general combining ability (GCA) effects. **P < 0.01. (EPS 1552 kb)
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Supplementary Figure S3: GCA effects for grain yield of the 135 parents plotted against their line per se performance for an index combining per se data on grain yield, plant height, heading time, and susceptibility to frost, lodging, yellow rust, leaf rust, powdery mildew and septoria tritici blotch with equal weight (○), which are commonly subject to early generation selection. Filled circles (●) represent lines with frost susceptibility < 6.5, disease susceptibility < 5, and belonging to the 70 % best lines regarding per se performance for grain yield, i.e. selection on independent culling levels. (EPS 465 kb)
Appendix
Appendix
Assume two unrelated base populations π1 (females) and π2 (males) with two alleles, no epistasis, no linkage and equilibrium within and among loci in the base populations. For hybrid breeding, the total genetic variance is then defined after Schnell (1965, 1982) as \(\sigma_{\text{G}}^{2} ({\text{hybrid}}) = \varphi^{\prime}\sigma_{{GCA^{\prime}}}^{2} + \varphi^{\prime\prime}\sigma_{{GCA^{\prime\prime}}}^{2} + \varphi^{\prime}\varphi^{\prime\prime}\sigma_{\text{SCA}}^{2}\), where \(\varphi^{\prime} = 1/2\left( {1 + F_{\pi 1} } \right)\) and \(\varphi^{\prime\prime} = 1/2\left( {1 + F_{\pi 2} } \right)\) refer to the probability that testcross lines received alleles identical by descent from π1 and π2, and F is the inbreeding coefficient of the respective population. Regarding the reciprocal recurrent selection of GCA, each heterotic group is tested with few elite testers from the opposite pool, e.g., numerous female parental lines with few male lines. Thus, for φ″, we need to consider the number of tester lines. Imagine the homozygous lines J and K, which will be combined in a single-cross tester. Consequently, φ″ = 1/2 + 1/2f jk , where f jk refers to the coefficient of coancestry among lines J and K. For three lines J, K, and L assuming theoretically an equal contribution of gametes to the tester, we get φ″ = 1/3 + 2/9(f jk + f jl + f lk ) and for arbitrary numbers of n lines, \(\varphi^{\prime\prime} = \frac{1}{n} + \frac{2}{{n^{2} }}\mathop \sum \nolimits_{j = 1}^{n - 1} \mathop \sum \nolimits_{k > 1}^{n} f_{jk}\). The value n represents the product of the number of testers multiplied by the number of tester lines (gametes) used to build up each tester, e.g., n = 4 for either using four inbred testers or two single-cross testers. The efficiency of type and number of tester lines with different relatedness [f jk = 0 (○), 0.25 (Δ) and 0.5 (×)] on the reduction of SCA is then determined relative to the use of one inbred tester as \({\text{Eff}} = 100 - \left[ {{{100 \times \left( {\varphi^{\prime}\varphi^{\prime\prime}\sigma_{\text{SCA}}^{2} + \varphi^{\prime}\varphi^{\prime\prime}\sigma_{{{\text{SCA}} \times {\text{E}}}}^{2} } \right)} \mathord{\left/ {\vphantom {{100 \times \left( {\varphi^{\prime}\varphi^{\prime\prime}\sigma_{\text{SCA}}^{2} + \varphi^{\prime}\varphi^{\prime\prime}\sigma_{{{\text{SCA}} \times {\text{E}}}}^{2} } \right)} {\left( {\varphi^{\prime}\sigma_{\text{SCA}}^{2} + \varphi^{\prime}\sigma_{{{\text{SCA}} \times {\text{E}}}}^{2} } \right)}}} \right. \kern-0pt} {\left( {\varphi^{\prime}\sigma_{\text{SCA}}^{2} + \varphi^{\prime}\sigma_{{{\text{SCA}} \times {\text{E}}}}^{2} } \right)}}} \right] = 100 - 100 \times \varphi^{\prime\prime}.\)
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Longin, C.F.H., Gowda, M., Mühleisen, J. et al. Hybrid wheat: quantitative genetic parameters and consequences for the design of breeding programs. Theor Appl Genet 126, 2791–2801 (2013). https://doi.org/10.1007/s00122-013-2172-z
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DOI: https://doi.org/10.1007/s00122-013-2172-z