Grain yield is a key economic driver of successful wheat production. Due to its complex nature, little is known regarding its genetic control. The goal of this study was to identify important quantitative trait loci (QTL) directly and indirectly affecting grain yield using doubled haploid lines derived from a cross between Hanxuan 10 and Lumai 14.
Ten yield-associated traits, including yield per plant (YP), number of spikes per plant (NSP), number of grains per spike (NGS), one-thousand grain weight (TGW), total number of spikelets per spike (TNSS), number of sterile spikelets per spike (NSSS), proportion of fertile spikelets per spike (PFSS), spike length (SL), density of spikelets per spike (DSS) and plant height (PH), were assessed across 14 (for YP) to 23 (for TGW) year × location × water regime environments in China. Then, the genetic effects were partitioned into additive main effects (a), epistatic main effects (aa) and their environment interaction effects (ae and aae) by using composite interval mapping in a mixed linear model.
Twelve (YP) to 33 (PH) QTLs were identified on all 21 chromosomes except 6D. QTLs were more frequently observed on chromosomes 1B, 2B, 2D, 5A and 6B, and were concentrated in a few regions on individual chromosomes, exemplified by three striking yield-related QTL clusters on chromosomes 2B, 1B and 4B that explained the correlations between YP and other traits. The additive main-effect QTLs contributed more phenotypic variation than the epistasis and environmental interaction. Consistent with agronomic analyses, a group of progeny derived by selecting TGW and NGS, with higher grain yield, had an increased frequency of QTL for high YP, NGS, TGW, TNSS, PFSS, SL, PH and fewer NSSS, when compared to low yielding progeny. This indicated that it is feasible by marker-assisted selection to facilitate wheat production.
Citation: Wu X, Chang X, Jing R (2012) Genetic Insight into Yield-Associated Traits of Wheat Grown in Multiple Rain-Fed Environments. PLoS ONE 7(2): e31249. doi:10.1371/journal.pone.0031249
Editor: Alfredo Herrera-Estrella, Cinvestav, Mexico
Received: December 16, 2010; Accepted: January 4, 2012; Published: February 17, 2012
Copyright: © 2012 Wu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Basic Research Program of China (2010CB951501), and the Generation Challenge Program (G7010.02.01). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Wheat (Triticum aestivum L.) is one of the most important crops in the world. Grain yield is the most important economic trait in wheat improvement. Being the final product of many processes, it is directly and multilaterally determined by yield-component traits, such as number of spikes per plant (NSP), number of grains per spike (NGS), one-thousand grain weight (TGW), and indirectly affected by other yield-related traits, e.g. plant architecture. Yield and yield associated traits are complex quantitative traits controlled by multiple genes and are highly influenced by environmental conditions . Some yield associated traits are less environmentally sensitive and have higher heritabilities than grain yield . Therefore, it is useful to examine yield associated traits when evaluating yield in order to gather specific information about the genetic control and relationship between yield and related traits crucial for sustained wheat improvement.
Quantitative trait locus (QTL) analysis has provided an effective way to dissect complicated quantitative traits into component loci and to study their individual effects on a specific trait . In a particular genetic background, QTL analysis allows the identification of QTLs that are environmentally relatively stable, thereby providing the breeder with targets for marker assisted variety improvement. QTLs for yield associated traits were previously reported in wheat –. Grain yield and yield associated traits were located on all chromosomes. However, the genetic basis for most of these traits is not well understood, particularly, epistatic QTL × QTL and QTL × environment interactions. A dissection of these interactions is needed to better understand the genetic control of these traits .
Drought is one of the most severe constraints to wheat production. Owing to increasing water shortages and uneven distribution of rainfall, it has become an increasingly important problem , . Additionally, under normal water conditions, grain yield is affected greatly by environment . Thus, it is meaningful to study the genetic control of yield-associated traits under a range of rain-fed and normal irrigation conditions.
Based on the mixed linear model  which partitions genetic effects into additive main effects (a), epistatic main effects (aa) and their environment interaction effects (QE, including ae and aae), the purpose of this study was to utilize the Hanxuan 10× Lumai 14 doubled haploid population to examine the genetic control of yield and yield-associated traits under different water-related conditions.
Phenotypic distribution of yield-associated traits
In the majority of environments Hanxuan 10 was significantly taller (PH 77.00–132.75 cm) and had more spikes (NSP 5.01–11.27), shorter spikes (SL 5.77–8.98 cm), denser spikelets (DSS 1.93–2.43), and fewer grains (NGS 23.94–38.65) than Lumai 14 (Table 1, File S1). Mean DH line values in the majority of environments for NSP, SL, DSS and NGS, and in all environments for PH, were between the parents. There was segregation for all ten traits in the DH population with the coefficients of variation (CV) ranging from 4.0 to 48.0%. All traits except TNSS (CV 5.0%–7.0%) were highly variable; NSSS was the most variable with CVs of 20.0%–48.0%. As DH progeny distribution is wider than the distribution of parental values, transgressive segregation occurred for all traits.
Correlations of yield-associated traits
For most environments, YP was significantly correlated with all traits, for example, positive correlations were observed between YP and NSP, NGS, TGW, TNSS, PFSS, SL, and PH (0.16*–0.52****), whereas there were negative correlations of YP with NSSS (−0.22**) and DSS (−0.19*) (Table 2). A positive correlation occurred between NGS and PFSS, TGW and PH, and TNSS and NSSS. Weak positive correlations also occurred between NSP and NSSS, between TNSS and DSS, and among NGS, TNSS and SL. The strongest correlation was observed between PFSS and NSSS with a negative correlation coefficient r = −0.98****. The negative correlation between SL and DSS was also highly significant (r = −0.85****). There were also significant negative correlations among NSP, NGS and TGW, between NSP and PFSS and PH, between NGS and NSSS, and between TGW and DSS, TNSS and PFSS.
Analysis of variance (ANOVA) for yield-associated traits
The ANOVA based on the general linear model for genotypes and year × location × water regime environments showed significant differences between genotypes and between environments for all ten traits (Table 3). The F-values for genotypes were 6.22 (P<0.0001) (YP) to 123.49 (P<0.0001) (PH) and for environments 245.66 (P<0.0001) (DSS) to 910.44 (P<0.0001) (TNSS). When ANOVA analysis for all traits was performed to determine the significances of differences between genotypes, between year × location (YL) combinations, between water regimes, and between two-factor combinations of genotypes, YL combinations and water regimes, it was clear that water regimes had a large effect on PH and NSP, but did not significantly affect NSSS and DSS. YL had large effects on YP, NGS, TGW, NSSS, PFSS, SL and DSS. The role of water regimes on TNSS was in line with YL (Table 4). The estimated heritabilities varied between 27.2% (YP) and 86.9% (DSS).
Genomic distribution of QTLs for yield-associated traits
A total of 241 QTLs controlling yield-associated traits were detected. The number of QTLs for individual traits ranged from 12 to 33 (Table 5). These were unevenly distributed on all chromosomes except 6D, on which no QTL was identified. They were more frequently observed on chromosomes 1B, 2B, 2D, 5A and 6B (more than 16 QTLs). The highest QTL number (22 or 9.1%) was identified on chromosome 2D, whereas the lowest number (2 or 0.8%) was on chromosome 4D. Chromosomes 2B and 7A possessed QTLs associated with all traits, whereas chromosomes 1D (DSS and PH) and 4D (SL and PH) possessed QTLs for only two traits. The number of QTLs on homoeologous groups 1 to 7 ranged from 27 (11.2%) to 48 (19.9%). The QTL frequency was the highest for the B genome with 104 (43.2%), and the lowest in the D genome with 45 (18.7%).
The map positions of QTLs for various yield-associated traits tended to cluster on each chromosome. Many QTLs attributed to correlated traits were clustered in relatively short intervals (10 cM) on chromosomes other than 3D and 6D (Figure 1). QTLs controlling correlated SL and DSS formed QTL clusters on chromosomes 2B, 2D, 3A, 4A, 5A and 7A. QTL clusters controlling PH and TGW were on 2B, 2D, 3A, 3B, 6B and 7B. QTL clusters for NSSS and PFSS were on 1B, 2A, 2B, 3A, 4B, 5A, 5B and 7A. Three QTL clusters associated with grain yield were located on chromosomes 1B, 2B and 4B. The QTL cluster at Xgwm131-1B - Xcwm70-1B was associated with six associated traits, viz. YP, NSP, NSSS, PFSS, SL and PH, and the favorable alleles of all a effect QTLs of YP, NSP, NSSS, PFSS and PH were contributed by the female parent Hanxuan 10. In contrast, the favorable alleles of all a effect QTLs in the P3615-160-2B - Xcwm529-2B and Xgwm107-4B - Xgwm149-4B clusters were from the male parent Lumai 14. The 2B group included seven traits (YP, NGS, TGW, PFSS, NSSS, SL and PH) whereas the 4B cluster involved six traits (YP, NSP, TNSS, NSSS, PFSS and SL) (Figure 1).
AddH, additive QTL contributed by Hanxuan 10; AddL, additive QTL contributed by Lumai 14; Epi, QTLs involved in epistatic effects. The bold line indicates the confidence intervals. All additive QTLs are shown; epistatic QTLs are those with large effects (i.e. the phenotypic variation explained (PVE)>the mean PVE of all main effects) and present in QTL clusters. Map distances in centiMorgans (cM) are shown on the left side of each chromosome.
Genetic main effects of QTL for yield-associated traits
Thirty three percent (PH) to 66.7% (YP) of QTLs were identified with significant a effects, and 50.0% (YP) to 97.0% (PH) of QTLs were involved in significant aa effects (Table 6). Of the identified a effect QTLs, a significant proportion (22.2% for PFSS - 90.9% for PH) was involved in epistatic interactions with background loci, whereas the majority (51.9% for TNSS - 100.0% for NSP) of loci involved in epistatic interactions did not appear to have significant additive effects (File S2). The a effects of Hanxuan 10 alleles increased NSP, SL, DSS, PFSS and PH at 52.6%–66.7% of loci, whereas those of Lumai 14 alleles increased YP, TGW and NGS at 62.5%–75.0% of loci, and the two parent alleles each increased TNSS and NSSS at 50.0% of loci (File S2). Of the aa effects, 52.9%–75.0% of epistatic pairs appeared to be recombinant for YP, TGW, NSSS, SL and PH, whereas 53.3%–66.7% of epistatic pairs were parental types for NSP, TNSS, PFSS and DSS. The frequencies of both recombinant and parental types for NGS were about 50.0% (File S2). This suggested that alleles increasing yield-associated traits were inherited from the two parents.
The a effect of a single QTL for an individual trait was equal to or more than the aa effect of a single epistasis, and the mean phenotypic variation explained due to the a effect exceeded that of aa effect (Table 6). Overall, the cumulative a effects controlling individual traits contributed more than aa effects (Figure 2). Thus, additive QTLs were more important than epistatic QTLs for all traits.
QTL × environment effects for yield-associated traits
For all traits, excluding DSS, 5.3% (SL) - 76.9% (TGW) of additive QTLs were involved in ae effects in 1–7 environments across all environments except hd99T (Haidian, Beijing in 1999 under drought stressed treatment (DS)), cp05T (Changping, Beijing in 2005 under DS) and cp06C (Changping, Beijing in 2006 under well-watered treatment (WW)), and for YP, NP, NGS, TGW, NSSS and PFSS, 11.8% (TGW) - 83.3% (NSP) of epistatic pairs were subjected to aae effects in one to three of the 11 environments (File S2).
Among additive QTLs involved in ae effects, even the absolute value of the ae effect of a single QTL for NSP, NGS, TGW, TNSS, SL and PH appeared less than the a effect, but for YP, PFSS and NSSS the ae effects were greater than the a effects (Table 7). QNSSS.cgb-4B had only ae effects contributed by Hanxuan 10 in environments fy01T (Fenyang, Shanxi in 2001 under DS) and fp99C (Fuping, Shaanxi in 1999 under WW), indicating it was induced by the environment. Thus, the additive effects for YP, PFSS and NSSS were readily affected by environments. In addition, owing to ae effects, Hanxuan 10 possessed alleles increasing YP, NSP, NGS, TGW, TNSS, PFSS, SL, and PH, and decreasing NSSS at one to six QTLs in one to three drought stressed environments, suggesting that these QTLs might adapt well to drought conditions (File S2). For example, QNGS.cgb-2B conferred positive ae effects in fy01T and hd05T (Haidian, Beijing in 2005 under DS), QTNSS.cgb-2D.1 in ly99T (Luoyang, Henan in 1999 under DS), fp99T (Fuping, Shaanxi in 1999 under DS) and fy01T, QPH.cgb-6B.6 in fp00T and fy01T, and QTGW.cgb-6B in ly99T, fp99T and fy01T. However, some QTLs controlling NSP, NGS, TGW, TNSS, SL and PH with a effects contributed far more phenotypic variation than ae effects (Table 8). They were less affected by environments and therefore might be beneficial to wheat genetic improvement. In general, the a effects (3.1%–38.0%) of all traits contributed more than ae effect (0.2%–4.1%) (Figure 2).
For epistatic QTLs involved in aae effects, generally the averaged absolute value of the aae effects detected for epistatic QTL pairs were larger than their aa effects, indicating that these epistatic pairs of YP, NSP, NGS, TGW, NSSS and PFSS were highly sensitive to environments (Table 7). Epistatic pairs between QTGW.cgb-5A.4 and QTGW.cgb-5B.2 showed positive effects in fy01T, and epistatic pairs between QNSSS.cgb-4B and QNSSS.cgb-6A.1 exhibited negative effects in fy01T. These epistatic effects were beneficial under drought conditions although they contributed very little (File S2). In addition, the total aa effects (2.3%–7.9%) accounted for more phenotypic variation than aae effects (0.4%–2.1%) for all traits except YP (Figure 2).
QTL response to selecting high NGS and TGW
Among four categories of progeny lines (high TGW and high NGS group (Hgw_Hgn), high TGW but low NGS group (Hgw_Lgn), low TGW but high NGS group (Lgw_Hgn) and low TGW and low NGS group (Lgw_Lgn)), significant differences occurred for all traits except YP, their F-values were 2.99 (P<0.05) - 28.05 (P<0.0001) respectively (Table 9). No significant differences observed for YP among four groups indicated that high yield may be achieved by various selection approaches. The comparison between the highest yielding group (Hgw_Hgn) and the lowest yielding group (Lgw_Lgn) suggested that the grain yield and grain weight in these high-yielding lines was associated with a combination of traits, including a heavier TGW and taller plants with a longer SL, a more TNSS, a higher PFSS, a sparser DSS but a fewer NSP and NSSS (Table 9). The two high grain weight groups have a significantly heavier TGW and taller PH than the other two groups, the Hgw_Hgn group has a significantly fewer TNSS than the Lgw_Hgn group. The two high grain number groups have a significantly longer SL, a higher PFSS but lower NSSS than the two low grain number groups. The Hgw_Hgn group has a more TNSS than the Hgw_Lgn group, and the Lgw_Hgn group has a more NGS but a sparser DSS than the Lgw_Lgn group.
QTL allele frequency at the 34 genomic regions associated with QTL for ten traits was assessed in the 41 progeny lines present in the four groups. The high-yielding progenies were enriched for QTL that resulted in increased YP (one of three QTL from Hanxuan 10), NSP (one QTL), NGS (two of four QTL), TGW (one of six QTL), TNSS (four of six QTL), PFSS (two of four QTL), SL (two of four QTL), DSS (one of three QTL) and PH (one QTL), and reduced NSSS (three QTL from Lumai 14) (Table 10). Of these 25 regions, five varied in frequency between the high and low grain weight groups, resulting in an increased frequency of QTL for higher NSP (one QTL from Hanxuan 10), TGW (one of two QTL), TNSS (one QTL), and DSS (one of two QTL); Seven regions varied between the high and low grain number groups, they were associated with more YP (one of two QTL), NGS (two of three QTL), TNSS (one of two QTL), PFSS (one QTL), SL (one of two QTL), PH (one QTL) and fewer NSSS (one QTL) in the high grain number groups.
Grain yield is a major goal for the improvement of wheat in drought-prone areas . Few reports show the genetic basis of yield-associated traits under different water conditions. Maccaferri et al. (2008) investigated the genetic basis of three traits (grain yield, heading date and plant height) in 249 durum wheat recombinant inbred lines in 10 rainfed and 6 irrigated environments . McIntyre et al. (2010) evaluated genomic regions of grain yield and yield-related components in 192 bread wheat recombinant inbred lines under 8 irrigated and rainfed conditions . By association mapping, the genetic basis of grain yield was dissected in a collection of 189 elite durum wheat accessions evaluated in 15 environments highly different for water availability . The present study identified QTL controlling ten yield-associated traits (yield, yield components and other agronomic traits) in a winter wheat DH population under a range of environments (14–23 year × location × water regime combinations) that differed widely in the amounts of available water. In our study, yield was defined as yield per plant as reported in other studies , . And the middle five plants in each plot being randomly sampled for analysis was to avoid burdensome measurement, which can represent the plot , although the number appeared less in comparison with other studies , .
Grain yield and yield associated traits are complex quantitative traits controlled by multiple genes and highly affected by environments . An important aspect of this study was the use of the mixed linear model to permit division of genetic effects into additive main effects (a effects), additive × additive epistatic main effects (aa effects) and their environmental interaction effects (ae, aae). To date, the majority of QTL studies in wheat have not examined interactions (ae, aa and aae) , –, –, , , , –. QTL analyses not enabling detection of these interactions would lead to biased estimates of main-effect QTLs, particularly for those involved in complex traits like yield. This could result in a lower than predicted genetic gain from marker-assisted selection as well as some difficulties when trying to isolate the QTL . The importance of epistasis and environmental interactions in the genetics of yield traits has been demonstrated in rice and maize , –. Results such as those of Zhuang et al. (2002) implied that the detection of QTLs with main effects, as well as the magnitude and directions of the additive effects, might vary depending on their interactions with other loci. Our study also confirmed that all traits evaluated were controlled by a effects, aa effects and environmental interaction effects (ae and/or aae), except for density of spikelets per spike (DSS) where no QTL × environment interaction effects (QE effects) were detected (Figure 2). We also found that many QTLs with additive effects were involved in interactions with other QTLs that were affected by genetic background (File S2). Although both a and aa effects contributed to the genetic basis of grain yield and other related traits in wheat, the cumulative contribution from significant aa effects (0.3%–16.5%) was small relative to that from a effects (3.1%–51.5%) for each trait investigated (Figure 2). Recent studies of yield-associated traits in rice and barley also showed that many epistatic effects were significant, but were all likewise small in magnitude relative to the additive effects , , . The low percentage of phenotypic variance explained by epistatic effects is apparently due to a large number of QTLs with small effects.
The genotype-by-environment interaction is important in determining the adaptation and fitness of genotypes in the physical environment . Numerous cases of such interactions have been documented , . In our study the DH population was evaluated in five locations over one to seven years with two water regimes. A few additive QTLs (for yield per plant (YP), number of spikes per plant (NSP), total number of spikelets per spike (TNSS), proportion of fertile spikelets per spike (PFSS), spike length (SL) and plant height (PH)) and epistatic interactions (for number of grains per spike (NGS), 1000-grain weight (TGW), number of sterile spikelets per spike (NSSS) and PFSS), and more than half the additive QTLs (for NGS, TGW and NSSS) and epistatic interactions (for YP and NSP) were involved in interactions with environments. QTL by year × location (YL) interaction effect was the major source of environmental interaction by further QTL mapping to detect QE interaction effects, including QTL by YL interaction under the same water regime, or QTL by water regime interaction under the same YL combination (data not shown). Several desirable QTLs detected under year × location × drought stress (DS) combination, such as QNGS.cgb-2B, QTNSS.cgb-2D.1 and QPH.cgb-6B.6, were identified with the consistent effects in the same year × location combinations under DS. But no QTL by water regime interactions were detected under the same YL combination, except that one QTL controlling YP on 2D (near Xwmc 453.1) was detected with negative ae effect (−0.57***) in hd99 (Haidian, Beijing in 1999). This indicated that water treatment contributed little to environmental variation in our study. The actual contributions of ae and/or aae interactions were small compared to a effects (Figure 2). Such an outcome is not only ideal for marker-assisted breeding but should facilitate their cloning in situations such as drought-prone environments . In the present study, twenty six major QTLs tagged by 19 flanking markers were identified with little or no environmental interactions, and contributing large phenotypic variation explained (PVE) (Table 8). For these QTLs, the increase in yield and yield-associated trait values ranged from 1.6% to 10.9% over the population mean. These QTLs could be the targets for marker assisted selection in wheat improvement. In our DH population, phenology effects were not considered owing to only 4 day difference at flowering date, 2–3 day difference at maturing date of 150 lines. The identification of QTLs may not be largely confounded by the low range of ‘pheno-environments’.
Consistent with other studies , QTLs governing grain yield and yield-associated traits in the present work were distributed on chromosomes in a non-random manner. The most QTLs (22) were identified on 2D, whereas only 2 QTLs were on 4D. Although no QTL was found on 6D in our study, QTLs controlling grain yield and yield components (NSP, TGW, NGS) were identified on that chromosome in other studies –, , . Failure to detect a QTL in our case might be because we had fewer markers on 6D, there was no segregation for trait differences involving that chromosome or the effect of a QTL was too small in a cross in which many other stronger QTLs were identified.
QTLs for yield-associated traits were likewise highly concentrated in a few chromosomal regions on the same chromosomes (Figure 1). These QTL clusters were generally involved in correlated traits. Similar associations were found in other grain yield component studies , , , , , , , . Clustered QTLs for YP, NSP and SL and sometimes NGS and TGW in the same region of chromosome 1B were reported by Börner et al. (2002), Huang et al. (2003), Kumar et al. (2007), Quarrie et al. (2005) and Wang et al. (2009) , , , , . All traits except NSSS and PFSS in yield-associated QTL clusters on 2B were observed by Habash et al. (2007), Huang et al. (2006), Kumar et al. (2007), Maccaferri et al. (2008) and McCartney et al. (2005) , , , , . The yield related QTL cluster on 4B was near the green revolution gene Rht-B1 locus and YP, NSP, NGS and TGW QTLs were also detected by others –, , , . The NSSS and PFSS QTLs concerning spikelet fertility in the above three QTL clusters on chromosome 1B, 2B and 4B were not reported previously. As the favorable alleles of the additive QTLs in these three clusters were from the same parents, we speculate that the clusters were preserved during long-term selection for grain yield, and we believed that they are of importance for grain yield determination. Additionally, we detected a yield QTL adjacent to a SL QTL and a QTL cluster involved in NGS, NSSS, PFSS and DSS on 7A. In other studies, not only were QTLs for YP, NGS and fertility-related traits detected, but they were associated with QTLs for NSP, TGW, TNSS and PH in the same bin , , , , , . This region appears to be important for grain yield because the favorable alleles of the additive QTLs were all from Lumai 14 and the majority of QTLs had strong effects. In addition, the yield-related QTL cluster (YP, SL and TNSS), with two clusters (NGS and PH) and (TGW, TNSS, SL and PH), was located in the centromere region of chromosome 2D YP, SL and TGW QTLs were detected in other studies , , , . The region Xwmc231-3B - Xgwm644.2-3B having epistatic QTLs for YP, TGW, SL and PH were found to have main-effect QTLs controlling YP, TGW, NGS, NSP in other studies , , , , . Based on these QTL clusters, it seems likely that such QTL clusters associated with yield are determinants of biomass , and that each yield component is determined at a different phase of plant development .
It is well-known that the reduced height gene (Rht), vernalization gene (Vrn) and photoperiod sensitivity gene (Ppd) have been the focus of yield breeding for many years as a means to reduce the height of the crop and to better adapt to their environments by flowering at the appropriate time . Therefore, it is not surprising to observe yield-related QTL clusters on 2B chromosome with Ppd-B1, 2D with Ppd-D1 and Rht8, and 4B with the green revolution gene Rht1 in our study. Ppd-B1 has been mapped 6.6 cM distal of Xgwm429 on 2B, and Ppd-D1 14.4 cM proximal of Xgwm261 near Rht8 on 2D . Rht1 was mapped near marker Xgwm165.1 on 4B .
Additionally, corresponding with the location of the vernalisation gene Vrn-A1 on 5A , two yield component related QTL clusters (TGW, NGS and PFSS) and (TNSS, NSSS, PFSS and PH) were located; TGW and TNSS were reported by others , , . On chromosome 3A distributed an earliness per se gene Eps-A1 affecting the plant development , two distinct yield component related QTL clusters (TGW, NGS and PH) and (NSP, NGS, NSSS, DSS and PFSS) were anchored in the same bin; TGW and NGS QTLs were also detected by others , , . The presence of NSSS and PFSS QTLs with large a effects in the two regions on 3A and 5A may indicate the genes affecting yield component such as TGW and/or NGS by influencing spikelet sterility. Lastly, it should be mentioned that we identified a QTL cluster (Xwmc269.3-6B - P4232.1-6B) involving QTLs for NSP, TGW and PH with strong a effects, which appears to be new.
Because yield per se is a complex trait with low heritability, breeding high yielding wheat cultivars by direct selection for yield has generally been slow . The coincidence of yield QTL with that of at least one yield component with high heritability offers a means for selecting for grain yield by efficient selection for one component . High heritabilities of the yield components were also observed in our study (Table 3). Additionally, due to genetic variation in yield and yield associated traits results from allelic segregations of many QTLs, those QTLs with large additive effects might result in larger difference in the traits of interest, which are valuable for breeders . Further, it indicated an altered frequency of QTL alleles consistent with the agronomic data that the high-yielding progeny lines had an increased frequency of QTL for increased grain yield, grain number, grain weight, total number of spikelets, proportion of fertile spikelets, spike length, plant height and fewer sterile spikelets and spikelets density than the low grain yielding progeny. The present results exhibited that potential improvement in yield and yield components could be made by selecting for some of the identified QTLs. These predictions should be validated by marker assisted selection for the identified component QTL followed by yield assessments.
QTL analysis showed that though yield-associated traits were subjected to additive main effects, epistatic main effects and their environmental modifications, the additive main-effect QTLs were the major genetic component. All chromosomes except 6D were observed with QTLs controlling yield-associated traits, but among different chromosomes QTLs were non-randomly distributed. A great number of QTLs were located on chromosome 1B, 2B, 2D, 5A and 6B. QTL cluster was another general characteristic of QTL distribution strikingly delegated by three yield-related QTL clusters on 1B, 2B and 4B which accounted for the correlations between YP and other traits well. Twenty six major QTLs with large phenotypic variation explained (PVE) could be the targets for marker assisted selection in wheat improvement. A small group high-yielding progeny was derived by selecting two major yield components TGW and NGS, which was rich in QTLs for higher YP, NGS, TGW, TNSS, PFSS, SL, PH and fewer NSSS than the low yielding progeny, indicating the potential of marker-assisted selection to facilitate wheat production later.
Materials and Methods
We have obtained the relevant permission for our field studies for growing the DH population and parents in three locations in China over 1 year from the corresponding institutions. They are the Luoyang Academy of Agricultural Sciences in Luoyang (ly) Henan, the Northwest Agriculture & Forest University in Fuping (fp) Shaanxi, and the Institute of Crop Science, Shanxi Academy of Agricultural Sciences in Fenyang (fy) Shanxi.
A doubled haploid population of 150 lines was developed by microspore culture from the F1 hybrid of Hanxuan 10 and Lumai 14, two Chinese common wheat cultivars . Hanxuan 10, a drought-tolerant cultivar from the Shanxi Academy of Agricultural Sciences, released in 1966, was still sporadically grown in arid and barren areas during the past decade. Lumai 14, a high-yielding cultivar adapted to abundant water and fertile conditions, was developed at the Yantai Institute of Agricultural Sciences, Shandong, and was widely grown in northern China during the 1990s. The phenology characteristics of the DH lines and their parents are similar. Flowering date of Hanxuan 10 is one day earlier than that of Lumai 14. The flowering date range of 150 DH lines is 4 day.
The DH population and parents were grown in five locations in China over 1, 2 and 7 years providing data for 12 year-location combinations (Table 11). The five locations include the experimental stations of the Institute of Crop Sciences, Chinese Academy of Agricultural Sciences in Haidian (hd) and in Changping (cp) Beijing, experiment stations of the Luoyang Academy of Agricultural Sciences in Luoyang (ly) Henan, the Northwest Agriculture & Forest University in Fuping (fp) Shaanxi, and the Institute of Crop Science, Shanxi Academy of Agricultural Sciences in Fenyang (fy) Shanxi. They are distributed in the different regions of northern China, including winter zone (Haidian and Changping in Beijing, Fenyang Shanxi) and facultative wheat zone (Luoyang Henan, and Fuping Shaanxi). They are characterized in terms of temperature, radiation, moisture and so on. For the nearest two locations in Beijing, wheat maturity in Haidian Beijing is 3–4 days earlier than in Changping Beijing generally because of the different temperature and rainfall. The 12 year-location trials were unevenly executed. Namely, most of 7 trials were conducted in Haidian Beijing, 2 trials were in Changping Beijing and 1 trial was in other three locations, only one year (1999–2000) with the most of three trials. We have obtained the relevant permission for our field studies for growing the DH population and parents in three locations in China over 1 year from the corresponding institutions. They are the Luoyang Academy of Agricultural Sciences in Luoyang (ly) Henan, the Northwest Agriculture & Forest University in Fuping (fp) Shaanxi, and the Institute of Crop Science, Shanxi Academy of Agricultural Sciences in Fenyang (fy) Shanxi.
In each year-location combination (YL), two water regimes were applied as drought stressed (DS) and well-watered (WW). DS treatments were represented by rain-fed conditions. The rainfalls are shown in Table 11. WW treatments were irrigated with 750 m3/ha four times: at the pre-overwintering, jointing, flowering and grain filling stages, respectively. All the DH lines, along with the parents were planted in Haidian (Beijing) in two-row plots with a length of 2 m and 30 cm spacing, whereas all lines were grown in four-row plots with a length of 4 m and 30 cm spacing in other locations. The field management followed standard agricultural practices. A total of 24 environments of year × location × treatments combination were investigated.
At maturity, five plants in the middle of each plot were randomly sampled for analysis. Eight traits (Table 12), including YP, NSP, NGS, TGW, TNSS, NSSS, SL and PH, were measured. Two derived traits, PFSS and DSS, were calculated as described in Table 12. For some external reasons, these traits were phenotyped in 14 to 23 environments (Table 12).
Statistical analysis was implemented using the SAS V8.0 statistics package (SAS Institute Inc., 1999). Pearson's correlation coefficients between pairs of traits were determined for each year × location × water regime environments and mean environment using the ‘proc corr’ procedure. The ANOVA-general linear model (GLM) analysis was performed to determine the significances of differences between DH line genotypes and between year × location × water regime environments. The broad sense heritability of each trait was determined as the ratio of genotypic variance to the sum of the genotypic and environmental variances. To further reveal the contribution of water treatment to phenotypic variation, ANOVA-GLM was carried out to determine the significances of differences between the genotypes, between year-location combinations, between water regimes, and between two-factor combinations (two-factor interactions) for genotypes, year-location combinations and water regimes. Year-location combination was considered as a separate factor because the two factors are not orthogonal (some years have only one location and vice versa).
The available genetic linkage map, established from the 150 DH lines using MAPMAKER/Exp version 3.0 software under Kosambis mapping function, consisted of 395 marker loci (132 amplified fragment length polymorphisms (AFLP) and 263 simple sequence repeats (SSR)) covering 3,904 cM with an average distance of 9.9 cM between adjacent markers –. QTL analysis was performed on line values for each trait. QTL detection was undertaken using the mixed linear composite interval mapping model in QTLNetwork 2.0 , . In the mixed linear model, the phenotypic value of the k-th DH line in environment h (yhk) can be expressed as the following:μ is the population mean; ai and aj are the additive effects (fixed effects) of two putative loci Qi and Qj, respectively; aaij is the additive × additive epistatic effect (fixed effect) between the two loci; , and are the coefficients of these genetic main effects; is the random effect of environment h with a coefficient ; (or ) is the random additive × environment interaction effect with a coefficient (or ) for Qi (or Qj); is the random epistasis × environment interaction effect with a coefficient ; is the random effect of marker f nested within the h-th environment with a coefficient , is the random effect of the l-th marker × marker interaction nested within the h-th environment with a coefficient ; is the random residual effect. The marker factors and in the model are used to absorb additive and epistatic effects of background QTLs for controlling the noise.
Composite interval analysis was carried out using forward-backward stepwise, multiple linear regression with a probability into and out of the model of 0.05 and a window size set at 10 cM. Significant thresholds for QTL detection were calculated for each dataset using 1,000 permutations and a genome-wide error rate of 0.05. The final genetic model incorporated significant main additive (a) and additive × additive epistatic genetic effects (aa) and their interactions with environment (ae and aae). In such a model, all possible pairs of markers were tested.
QTL frequency was estimated for different traits in 41 high-yielding lines (25% selection intensity), including having either high TGW and high NGS (Hgw_Hgn) (four lines), high TGW but low NGS (Hgw_Lgn) (thirteen lines), low TGW but high NGS (Lgw_Hgn) (fifteen lines), or low TGW and low NGS (Lgw_Lgn) (nine lines) as described in Rattey et al. (2009)  and McIntyre et al. (2010) . Each putative QTL was represented by its nearest marker, and the frequency of its desirable allele was calculated in the four groups of lines.
Phenotypic values of yield-associated traits in the wheat parents and DH Lines in different environments.
QTLs affecting yield-associated traits of wheat in different environments. This is the original QTL mapping results for ten yield-associated traits of wheat in more than 14 year × location × water regime environments.
We thank Professor Robert A. McIntosh (Plant Breeding Institute, University of Sydney, NSW, Australia) for revising the manuscript. We acknowledge Dr. Haiming Xu (Zhejiang University, China) for kind advice regarding the use of mapping software and data analysis. We are grateful to Professors Canjun Zhang, Suiqi Zhang, and Lianzhong Zuo for their kind and aborative managements of the plant materials in respective Luoyang (ly), Fuping (fp) and Fenyang (fy) locations.
Conceived and designed the experiments: RJ. Performed the experiments: XC XW. Analyzed the data: XW. Contributed reagents/materials/analysis tools: RJ XC. Wrote the paper: XW.
- 1. Shi J, Li R, Qiu D, Jiang C, Long Y, et al. (2009) Unraveling the complex trait of crop yield with quantitative trait loci mapping in Brassica napus. Genetics 182: 851–861.
- 2. Cuthbert JL, Somers DJ, Brule-Babel AL, Brown PD, Crow GH (2008) Molecular mapping of quantitative trait loci for yield and yield components in spring wheat (Triticum aestivum L.). Theor Appl Genet 117: 595–608.
- 3. Doerge RW (2002) Mapping and analysis of quantitative trait loci in experimental populations. Nat Genet 3: 43–52.
- 4. Shah MM, Gill KS, Baenziger PS, Yen Y, Kaeppler SM, et al. (1999) Molecular mapping of loci for agronomic traits on chromosome 3A of bread wheat. Crop Sci 39: 1728–1732.
- 5. Araki E, Miura H, Sawada S (1999) Identification of genetic loci affecting amylose content and agronomic traits on chromosome 4A of wheat. Theor Appl Genet 98: 977–984.
- 6. Kato K, Miura H, Sawada S (2000) Mapping QTLs controlling grain yield and its components on chromosome 5A of wheat. Theor Appl Genet 101: 1114–1121.
- 7. Börner A, Schumann E, Furste A, Coster H, Leithold B, et al. (2002) Mapping of quantitative trait loci determining agronomic important characters in hexaploid wheat (Triticum aestivum L.). Theor Appl Genet 105: 921–936.
- 8. Campbell BT, Baenziger PS, Gill KS, Eskridge KM, Budak H, et al. (2003) Identification of QTLs and environmental interactions associated with agronomic traits on chromosome 3A of wheat. Crop Sci 43: 1493–1505.
- 9. Groos C, Robert N, Bervas E, Charmet G (2003) Genetic analysis of grain protein-content, grain yield and thousand-kernel weight in bread wheat. Theor Appl Genet 106: 1032–1040.
- 10. Sourdille P, Cadalen T, Guyomarch H, Snape JW, Perretant MR, et al. (2003) An update of the Courtot × Chinese spring intervarietal molecular marker linkage map for the QTL detection of agronomic traits in wheat. Theor Appl Genet 106: 530–538.
- 11. Huang X, Coster H, Ganal MW, Röder MS (2003) Advanced backcross QTL analysis for the identification of quantitative trait loci alleles from wild relatives of wheat (Triticum aestivum L.). Theor Appl Genet 106: 1379–1389.
- 12. Huang X, Kempf H, Ganal MW, Röder MS (2004) Advanced backcross QTL analysis in progenies derived from a cross between a German elite winter wheat variety and synthetic wheat (Triticum aestivum L.). Theor Appl Genet 109: 933–943.
- 13. Huang X, Cloutier S, Lycar L, Radovanovic N, Humphreys DG, et al. (2006) Molecular detection of QTLs for agronomic and quality traits in a doubled haploid population derived from two Canadian wheats (Triticum aestivum L.). Theor Appl Genet 113: 753–766.
- 14. Quarrie SA, Steed A, Calestani C, Semikhodskii A, Lebreton C, et al. (2005) A high-density genetic map of hexaploid wheat (Triticum aestivum L.) from the cross Chinese Spring × SQ1 and its use to compare QTLs for grain yield across a range of environments. Theor Appl Genet 110: 865–880.
- 15. Quarrie S, Pekic Quarrie S, Radosevic R, Rancic D, Kaminska A, et al. (2006) Dissecting a wheat QTL for yield present in a range of environments: from the QTL to candidate genes. J Exp Bot 57: 2627–2637.
- 16. Marza F, Bai GH, Carver BF, Zhou WC (2006) Quantitative trait loci for yield and related traits in the wheat population Ning7840 × Clark. Theor Appl Genet 112: 688–698.
- 17. Narasimhamoorthy B, Gill BS, Fritz AK, Nelson JC, Brown-Guedira GL (2006) Advanced backcross QTL analysis of a hard winter wheat × synthetic wheat population. Theor Appl Genet 112: 787–796.
- 18. McIntyre CL, Mathews KL, Rattey A, Chapman SC, Drenth J, et al. (2010) Molecular detection of genomic regions associated with grain yield and yield-related components in an elite bread wheat cross evaluated under irrigated and rainfed conditions. Theor Appl Genet 120: 527–541.
- 19. Carlborg Ö, Haley CS (2004) Epistasis: too often neglected in complex trait studies? Nature Reviews Genetics 5: 618–625.
- 20. Araus JL, Villegas D, Aparicio N, García del Moral LF, El Hani S, et al. (2003) Environmental factors determining carbon isotope discrimination and yield in durum wheat under mediterranean conditions. Crop Sci 43: 170–180.
- 21. Maccaferri M, Sanguineti MC, Corneti S, Ortega JL, Salem MB, et al. (2008) Quantitative trait loci for grain yield and adaptation of durum wheat (Triticum durum Desf.) across a wide range of water availability. Genetics 178: 489–511.
- 22. Ceccarelli S, Acevedo E, Grando S (1991) Breeding for yield stability in unpredictable environments: Single traits, interaction between traits, and architecture of genotypes. Euphytica 56: 169–185.
- 23. Yang J, Zhu J, Williams RW (2007) Mapping the genetic architecture of complex traits in experimental populations. Bioinformatics 23: 1527–1536.
- 24. Maccaferri M, Sanguineti MC, Demontis A, El-Ahmed A, Garcia del Moral L, et al. (2011) Association mapping in durum wheat grown across a broad range of water regimes. J Exp Bot 62: 409–438.
- 25. Zhuang J, Fan Y, Rao Z, Wu J, Xia Y, et al. (2002) Analysis on additive effects and additive-by-additive epistatic effects of QTLs for yield traits in a recombinant inbred line population of rice. Theor Appl Genet 105: 1137–1145.
- 26. Tan L, Zhang P, Liu F, Wang G, Ye S, et al. (2008) Quantitative trait loci underlying domestication- and yield-related traits in an Oryza sativa × Oryza rufipogon advanced backcross population. Genome 51: 692–704.
- 27. Thomson MJ, Tai TH, McClung AM, Lai XH, Hinga ME, et al. (2003) Mapping quantitative trait loci for yield, yield components and morphological traits in an advanced backcross population between Oryza rufipogon and the Oryza sativa cultivar Jefferson. Theor Appl Genet 107: 479–493.
- 28. Wang R, Hai L, Zhang X, You G, Yan C, et al. (2009) QTL mapping for grain filling rate and yield-related traits in RILs of the Chinese winter wheat population Heshangmai × Yu8679. Theor Appl Genet 118: 313–325.
- 29. Habash DZ, Bernard S, Schondelmaier J, Weyen J, Quarrie SA (2007) The genetics of nitrogen use in hexaploid wheat: N utilisation, development and yield. Theor Appl Genet 114: 403–419.
- 30. McCartney CA, Somers DJ, Humphreys DG, Lukow O, Ames N, et al. (2005) Mapping quantitative trait loci controlling agronomic traits in the spring wheat cross RL4452 × ‘AC Domain’. Genome 48: 870–883.
- 31. Mathilde C, Jamila Cb, Laurent L, Michel B, Frédéric H (2007) Both additivity and epistasis control the genetic variation for fruit quality traits in tomato. Theor Appl Genet 115: 429–442.
- 32. Xing Z, Tan F, Hua P, Sun L, Xu G, et al. (2002) Characterization of the main effects, epistatic effects and their environmental interactions of QTLs on the genetic basis of yield traits in rice. Theor Appl Genet 105: 248–257.
- 33. Ma X, Tang J, Teng W, Yan J, Meng Y, et al. (2007) Epistatic interaction is an important genetic basis of grain yield and its components in maize. Mol Breeding 20: 41–51.
- 34. Li Z, Pinson SR, Park WD, Paterson AH, Stansel JW (1997) Epistasis for three grain yield components in rice (Oryza sativa L.). Genetics 145: 453–465.
- 35. Xu S, Jia Z (2007) Genome wide analysis of epistatic effects for quantitative traits in barley. Genetics 175: 1955–1963.
- 36. Kumar N, Kulwal PL, Balyan HS, Gupta PK (2007) QTL mapping for yield and yield contributing traits in two mapping populations of bread wheat. Mol Breeding 19: 163–177.
- 37. Lanceras JC, Pantuwan G, Jongdee B, Toojinda T (2004) Quantitative trait loci associated with drought tolerance at reproductive stage in rice. Plant Physiol 135: 384–399.
- 38. Reynolds M, Manes Y, Izanloo A, Langridge P (2009) Phenotyping approaches for physiological breeding and gene discovery in wheat. Ann Appl Biol 155: 309–320.
- 39. Peng J, Ronin Y, Fahima T, Roder MS, Li Y, et al. (2003) Domestication quantitative trait loci in Triticum dicoccoides, the progenitor of wheat. Proc Natl Acad Sci U S A 100: 2489–2494.
- 40. Kuchel H, Williams KJ, Langridge P, Eagles HA, Jefferies SP (2007) Genetic dissection of grain yield in bread wheat. I. QTL analysis. Theor Appl Genet 115: 1029–1041.
- 41. Ma Z, Zhao D, Zhang C, Zhang Z, Xue S, et al. (2007) Molecular genetic analysis of five spike-related traits in wheat using RIL and immortalized F2 populations. Mol Gen Genomics 277: 31–42.
- 42. Slafer G (2003) Genetic basis of yield as viewed from a crop physiologist's perspective. Ann Appl Biol 142: 117–128.
- 43. Bradshaw JE, Hackett CA, Pande B, Waugh R, Bryan GJ (2008) QTL mapping of yield, agronomic and quality traits in tetraploid potato (Solanum tuberosum subsp. tuberosum). Theor Appl Genet 116: 193–211.
- 44. Jing R, Chang X, Jia J, Hu R (1999) Establishing wheat doubled haploid population for genetic mapping by anther culture. Biotechnology 9: 4–8.
- 45. Hao Z, Chang X, Guo X, Jing R, Li R, et al. (2003) QTL mapping for drought tolerance at stages of germination and seedling in wheat (Triticum aestivum L.) using a DH population. Agricultural Sciences in China 2: 943–949.
- 46. Zhou X, Jing R, Hao Z, Chang X, Zhang Z (2005) Mapping QTL for seedling root traits in common wheat. Scientia Agricultura Sinica 38: 1951–1957.
- 47. Yang D, Jing R, Chang X, Li W (2007) Identification of quantitative trait loci and environmental interactions for accumulation and remobilization of water-soluble carbohydrates in wheat (Triticum aestivum L.) stems. Genetics 176: 571–584.
- 48. Wang D, Zhu J, Li Z, Paterson AH (1999) Mapping QTLs with epistatic effects and QTL × environment interactions by mixed linear model approaches. Theor Appl Genet 99: 1255–1264.
- 49. Rattey A, Shorter R, Chapman S, Dreccer F, Herwaarden Av (2009) Variation for and relationships among biomass and grain yield component traits conferring improved yield and grain weight in an elite wheat population grown in variable yield environments. Crop & Pasture Science 60: 717–729.