Zhang Dale1,2†
He Jie
Li Suoping- 1School of Life Science, Henan University, Kaifeng, China
- 2Institute of Plant Stress Biology, Henan University, Kaifeng, China
The seed dormancy characteristic is regarded as one of the most critical factors for pre-harvest sprouting (PHS) resistance. As a wild wheat relative species, Aegilops tauschii is a potential genetic resource for improving common wheat. In this study, an advanced backcross population (201 strains) containing only Ae. tauschii segments was developed by means of synthetic octaploid wheat (hexaploid wheat Zhoumai 18 × Ae. tauschii T093). Subsequently, seed dormancy rate (Dor) in the advanced backcross population was evaluated on the day 3, 5 and 7, in which 2 major QTLs (QDor-2D and QDor-3D) were observed on chromosomes 2D and 3D with phenotypic variance explained values (PVEs) of 10.25 and 20.40%, respectively. Further investigation revealed significant correlation between QDor-3D and Tamyb10 gene, while no association was found between the former and TaVp1 gene, implying that QDor-3D site could be of closer position to Tamyb10. The obtained quantitative trait locus sites (QTLs) in this work could be applied to develop wheat cultivars with PHS resistance.
Introduction
As a serious natural disaster, pre-harvest sprouting (PHS) is featured by seed germination occurring in spikes before wheat harvest (Sharma et al., 1994), leading to consumption of seed storage material, reduction of grain weight as well as degradation of nutrition and processing quality (Groos et al., 2002). In China, PHS has caused severe damage in many areas including the middle and lower reaches of the Yangtze river, southwest winter wheat and northeast spring wheat regions, due to conventional abundant rains in harvest season (Xiao et al., 2002). Unexpectedly, this situation has occasionally happened in the Huanghuai and north winter wheat regions in recent years. Therefore, breeding PHS resistant varieties has emerged as one of the major objectives to overcome this challenge, particularly for the wet and humid regions in harvest season (Liu et al., 2016).
Resistance to PHS is known to be linked to multi-factors including seed coat color, seed dormancy time, spike characteristics (spikelet density and awn length), germination inhibition substances of glume, alpha amylase activity, abscisic acid (ABA), and gibberellic acid (GA), etc., among which seed dormancy characteristic is regarded as one of the most critical factors for PHS resistance (Mares and Mrva, 2001; Gatford et al., 2002; Kottearachchi et al., 2006; Tan et al., 2006; Munkvold et al., 2009; Liu et al., 2017). Seed dormancy is a complex trait, as it can be affected by genetic background/gene combinations, as well as environmental conditions (Jaiswal et al., 2012; Kulwal et al., 2012). Therefore, a single major gene or quantitative trait locus (QTL) for seed dormancy cannot comprehensively explain the genetic diversity of wheat varieties. Up to now, QTLs for seed dormancy have been identified on each of the 21 chromosomes of wheat genome utilizing various mapping populations (Mares and Mrva, 2014). Most major QTLs are located on chromosomes 2B (Munkvold et al., 2009; Chao et al., 2010; Somyong et al., 2014), 3A (Mori et al., 2005; Liu et al., 2013), and 4A (Mares et al., 2005; Chen et al., 2008; Ogbonnaya et al., 2008; Torada et al., 2008; Mohan et al., 2009; Rasul et al., 2009; Cao et al., 2016). Major QTLs for PHS were also detected on chromosome 3D of red kernels wheat and 2D of synthetic hexaploid wheat (Groos et al., 2002; Ren et al., 2008). In addition, TaVp1 and Tamyb10 genes for PHS resistance have been identified in bread wheat, which are located on the long arms of chromosomes 3A, 3B, and 3D, respectively (Xia et al., 2009; Himi et al., 2011; Sun et al., 2012). TaVp1 gene also performs the multi-functions of advancing embryo dormancy and repressing germination, besides promoting embryo maturation (McCarty et al., 1991). Tamyb10 gene is found to be a transcription factor to regulate the flavonoid biosynthetic pathway, controlling proanthocyanidin synthesis in testa. PHS resistance is closely related with the red pigmentation, which could be possibly attributed to the pleiotropic effect of this gene (Himi et al., 2002).
Aegilops tauschii Cosson (DD, 2n = 2x = 14), the diploid progenitor of common wheat, is an annual, self-pollinated plant with high level of genetic variability for disease-resistance, productivity traits and abiotic stress resistance (Sukhwinder et al., 2012). It has a wide natural distribution in central Eurasia, spreading from northern Syria and Turkey to western China. In China, this species mainly distributes in Yili area of Xinjiang and middle reaches of the Yellow River (including Shanxi and Henan provinces) (Wei et al., 2008). The genetic variation of Ae. tauschii is more abundant than that of wheat D genome since only Ae. tauschii in certain distribution areas are involved in the origin of common wheat (Wang et al., 2013). Therefore, analogous to other wild crop progenitors, Ae. tauschii is considered as a prospective gene donor for improving common wheat (Kilian et al., 2011).
Many superior genes of Ae. tauschii have been transferred into common wheat by taking synthetic hexaploid wheat (tetraploid wheat × Ae. tauschii) as a “bridge” (Miranda et al., 2007). Actually, previous studies indicated that lots of QTLs from synthetic hexaploid wheat had been identified and some were found located on the D genome by utilizing advanced backcross population or introgression lines (Pestsova et al., 2006; Kunert et al., 2007; Naz et al., 2008; Yu et al., 2014). Alternatively, desirable traits may also be transferred from Ae. tauschii to common wheat via direct crossing (Miranda et al., 2007). Gill and Raupp (1987) proposed the first systematic direct gene transfer protocol. Though wheat genomes A, B, and D could be improved concurrently through hybridization of synthetic hexaploid wheat with common wheat, the interesting target alleles in Ae. tauschii could be transferred into common wheat through direct crossing, avoiding interference of adaptive allelic combinations from the other A and B genomes. However, only a few studies focused on this strategy due to its high sterility in hybrid F1 from distant hybridization and extremely low ripening rates in backcross between hybrid F1 and recurrent parent (Cox et al., 1990; Fritz et al., 1995; Olson et al., 2013). As a feature of this work, synthetic octaploid wheat (AABBDDDD, 2n = 8x = 56) was proposed as a “bridge” to overcome the above challenge through chromosome doubling of hybrid F1 obtained from the cross of Ae. tauschii and common wheat. In this study, an advanced backcross population containing only Ae. tauschii segments was developed through backcross of synthetic octaploid wheat with recurrent parent, which could effectively broaden the genetic background of common wheat. Meanwhile, QTLs for seed dormancy from Ae. tauschii were located in the population, and the obtained strains with seed dormancy characteristics could also provide novel genetic resource for PHS-resistance in wheat breeding.
Materials and Methods
Plant Material
The diploid Ae. tauschii ssp. tauschii accession T093 was originally derived from Henan province, which is resistant to PHS with long seed dormancy time after harvest. Zhoumai 18, a typical white-grain wheat with high susceptibility to PHS, was applied as recurrent parent in this work. Hybrid F1 plants were obtained through hybridization of Ae. tauschii accession T093 as female parents with Zhoumai 18, which were then treated with colchicine to generate synthetic octaploid wheat (AABBDDDD, 2n = 8x = 56). The next year, emasculated florets of Zhoumai 18 were pollinated by synthetic octaploid wheat to generate BC1F1 seeds. Afterwards, the BC1F1 plants, as female parents, were successively backcrossed two times by Zhoumai 18 and then selfed four generations to produce advanced backcross population (BC3F4 population) (Figure 1). Phenotypic traits of strains within the group were stabilized after several generations of backcross and selfing, demonstrating consistent ripening rates with the recurrent parent Zhoumai 18. The mapping population and Zhoumai 18 were cultivated on the 2014–2015 crop season in the wheat breeding farm of Plant Germplasm Resources and Genetic Engineering Laboratory, Henan University. Seeds were sown with 10 cm distance between plants and 30 cm row gap, which were grown under consistent field conditions.
Figure 1. A crossing scheme for obtaining advanced backcross population through the “bridge” of synthetic octaploid wheat. Dt highlighted in blue designates the genome of Ae. tauschii.
Map Construction and QTL Analysis
DNA was extracted from the fresh leaves of advanced backcross population and Zhoumai 18 in 2014 according to the method described previously (Olson et al., 2013). The genetic map was constructed based on the physical positions of simple sequence repeat (SSR) markers from wheat D genome (http://wheat.pw.usda.gov/cgi-bin/GG3/), in which the S19676-2 marker (F: CACTCAGCCAACCCAGGAAA, R: CAAATAGTTCTATCACTTGGTCTCCC) was exploited by utilizing the Ae. tauschii genome sequences (Jia et al., 2013). PCR reactions for SSR were performed using the method described by Röder et al. (1998). SSR markers were anchored and grouped to the seven Ae. tauschii chromosomes through sequence alignment between the primers and reference genome. The calculation of segment lengths and genome ratios was referred to the method described by Liu et al. (2006). The QTLs for seed dormancy were identified utilizing QTL IciMapping Ver 4.0 (Meng et al., 2015). RSTEP-LRT-ADD mapping (stepwise regression-based likelihood ratio test for additive QTL) was adopted and a significant threshold of likelihood of odds (LOD) was estimated by running 1,000 permutations with a type I error of 0.05.
Amplification and Analysis of TaVp1 and Tamyb10 Genes
Two pairs of primers, TaVp1-4-F1 (5′-TCTTGGTTCACTCGTTAGCATC-3′) + Vp1-4-R1 (5′- CATTCTGCTCTTGTT GTTGGG-3′) and Tamyb10-5-F1 (5′-AAGGAATGCGGCAAGAGTGA-3′) + Tamyb10-5-R1 (5′-TCCTCCACGACCAAAGACCC-3′), were designed from the available sequences of TaVp1D (Genbank ID: AJ400714) and Tamyb10-D1 (Genbank ID: KP279637), respectively. PCR reactions were performed using the method described by Röder et al. (1998). The physical positions of TaVp1D and Tamyb10-D1 were determined based on the sequence alignment with Ae. tauschii reference genome. QTLs for seed dormancy of the former were checked in the advanced backcross population utilizing QTL IciMapping Ver 4.0. The correlation between PCR fragments from the latter and seed dormancy was analyzed by Wilcoxon rank sum test.
Phenotypic Evaluation
Five spikes from each line were harvested at day-40 post anthesis (40-dpa), and dried indoors for 5 days at ambient humidity and temperature, which were then manually threshed and placed at −20°C to preserve dormancy for 2 weeks due to slight differences in maturity. Fifty seeds were placed on moistened filter paper in a petri dish (150 mm diameter) and incubated in the dark. The Dor values were evaluated by germination test under room temperature (25°C) on the 3, 5, and 7 days, respectively, based on the method described by Cao et al. (2016) [Dor (%) = 100–GR (%) (GR: germination rate)]. The experiment was conducted with two replicates and the Dor was presented as the arithmetic mean values. The GR of each treatment was calculated using the following formula: GR = G/N, in which G and N stand for the numbers of germinated seeds and the total seeds in a given petri dish, respectively. With regard to lines with rather low germination rate value (≤5%), the remaining seeds were treated with 1 mL of 10 mM gibberellic acid and were then placed at 4°C for 3 days to break dormancy. Afterwards, they were transferred back at room temperature (25°C) and assessed for germination 10 days later. Lines which had not germinated were considered inviable and excluded for further calculation.
Statistical Analysis
Statistical analysis was performed on IBM® statistics 19 (SPSS Inc.,), including Friedman test, Wilcoxon rank sum test, and correlation coefficient (Pearson correlation). The significant difference of seed dormancy rate among correlated samples on the three detections was assessed by Friedman test, while that between two independent samples based on amplified fragments from Tamyb10-5F1/Tamyb10-5R1 was evaluated by Wilcoxon rank sum test.
Results
Polymorphism Marker on the D Genome and Number of Introgressed Segments
Two hundred and one BC3F4 lines were successfully genotyped by SSR markers. Altogether 1114 SSR markers were used to detect polymorphism between the donor parent Ae. tauschii T093 and the recurrent parent Zhuomai 18. Among them, polymorphism between the two parents was detected in 374 SSR markers, in which 104 of them were confirmed to be polymorphic in the advanced backcross population, accounting for 27.8%, with an average of 14.9 markers for each chromosome (Table 1). Most of the polymorphic markers were observed on chromosome 5D with the total number of 36, whereas the least was found on chromosome 1D and 4D with the total number of only 6. Besides the unidentified 70 markers, a physical map was constructed based on the 304 polymorphic SSR markers between parents (Figure 2), which displayed heterogeneous distribution on 7 linkage groups of D genome, with a total length of 4004.5 Mb. The physical map illustrates an average interval of 36.2 Mb among 104 polymorphic markers in the population, while these markers also exhibit inhomogeneous distribution in different chromosome regions. Specifically, some markers concentrate in the same region with a very short distance, demonstrating a minimum gap of only 0.8 Mb or even no recombination events between them. However, huge long distances were also found for some other markers. For instance, the distance between markers Xgdm72 and Xbarc42 on chromosome 3D is determined to be 416.1 Mb.
Table 1. The size of introgressed segments detected in the advanced backcross population and cumulative proportion in the donor genome.
Figure 2. Physical map constructed based on the 304 polymorphic SSR markers between parents. Polymorphic markers in the advanced backcross population are highlighted in red. The unit of distance is megabasepairs (Mb).
Altogether 1,522 chromosome segments from Ae. tauschii were detected in the advanced backcross population (201 lines). Specifically, no segment was found in 39 lines (19.4%). While the remaining 162 lines (80.6%) contain 1363 homozygous and 159 heterozygous segments, with an average of 8.41 homozygous and 0.98 heterozygous segments in each line (Table S1, Figure S1). Only a single introgressed segment was observed in 34 lines, and 2 segments were identified in 19 lines. According to the physical positions of SSR markers, the size of each introgressed segment in the lines and ratios accounting for the whole donor genome were estimated (Table 1). The introgressed segments range from 1.0 to 60.5 Mb, with an average size of 15.4 Mb in homozygous and 13.5 Mb in heterozygous. In addition, the distribution of chromosome segment from Ae. tauschii exhibited a significant difference in wheat D genome (Figure S2). Typically, the introgression fragments from 4D of Ae. tauschii contain the least 27 fragments, only accounting for 1.8%. Whereas those from 5D occupy the most 713 fragments, accounting for 46.8%. The results herein clearly confirm that the chromosome segments of Ae. tauschii have been transferred into common wheat by means of synthetic octaploid wheat (Ae. tauschii T093 × Zhoumai18), which effectively broadens the genetic background of common wheat.
Evaluation of Seed Dormancy Rate
Seed dormancy rate (Dor) from 201 lines in the advanced backcross population was examined on the day 3, 5, and 7 (Table S2). Similar frequency distribution of Dor from 201 lines could be observed in the three detections (Figure 3), in which the most intensive distribution consistently located at rather low value (Dor ≤ 5%). For the long seed dormancy (Dor > 90%), the proportions were determined to be 10.9, 8.9, and 6.9%, respectively, for the day 3, 5, and 7. While as marked by the black arrows, the respective seed dormancy rates of the recurrent parent Zhoumai 18 were 44, 28, and 20% in the parallel experiment, indicating that the PHS-resistance strains are contained in the advanced backcross population. Phenotypic correlations among the obtained seed dormancy rates for the three detections were further analyzed through Pearson coefficient. As shown in Table 2, each pair of Dor exhibits high positive correlation with coefficient no <0.98. The correlation coefficients for 2 replicates were shown in Table S3. The higher positive correlation coefficient, the less Dor is affected by the external environment factors in this experiment. Additionally, Friedman test of Dor among the lines show highly significant difference (P < 0.01) for the three detections, implying minor phenotypic detection error for the obtained phenotype data.
Figure 3. Frequency distributions of seed dormancy rate (Dor) of the advanced backcross population on the day 3, 5, and 7. Red: seed dormancy rate on the day 3; Blue: seed dormancy rate on the day 5; Green: seed dormancy rate on the day 7. Black arrows indicate the mean values of Dor from Zhoumai 18.
Table 2. Correlation coefficients among three time periods associated with Dor in the advanced backcross population.
QTL Analysis of Seed Dormancy Rate
To elucidate the genetic control for seed dormancy traits associated with PHS resistance, two major QTLs (QDor-2D and QDor-3D) were located on Xwmc503 of 2D and Xcfd223 of 3D by QTL IciMapping software in three detections under the single environment (Figure 4, Table 3). As listed in Table 3, the positive alleles of additive effect are derived from Ae. tauschii, further underscoring the valuable genes in Ae. tauschii as wheat wild resource (Sukhwinder et al., 2012). The QDor-2D displays the phenotypic variance explained values (PVEs) of 6.59, 6.02, and 5.64% in the three detections, respectively, corresponding to the additive effect values of 25.13, 23.50, and 22.02. As for QDor-3D, the PVE demonstrates prominently enhanced values of 13.83, 12.58, and 11.77%, with the additive effect values of 20.91, 19.50, and 18.27. Apparently, QTL detection for Dor could explain more phenotypic variance on the 3rd day compared with the other two measurements, implying the most prominent difference in the seed dormancy among lines in this detection.
Figure 4. Positions of putative QTLs detected on the day 3, 5, and 7 in the advanced backcross population. Black: LOD of QTLs on the day 3; Red: LOD of QTLs on the day 5; Green: LOD of QTLs on the day 7.
Table 3. Analysis of putative QTLs for seed dormancy traits in the advanced backcross population.
Correlation Analysis of TaVp1, Tamyb10 Genes and Seed Dormancy
The genotypes of 201 strains in the advanced backcross population were analyzed through TaVp1-4F1/TaVp1-4R1 and Tamyb10-5F1/Tamyb10-5R1 primers (Figure 5). The former displayed co-dominant marker with two amplified fragments (282 bp from Ae. tauschii and 423 bp from Zhoumai 18), which was afterwards located on chromosome 3D by Ae. tauschii genome map (Figure 2). The LOD value of this site was found to be <3.0 (Table 3), demonstrating little correlation of TaVp1 with seed dormancy traits. As could be observed in Figure 5, 389 bp fragment was amplified only from Ae. tauschii in the advanced backcross population by the dominant markers Tamyb10-5F1/Tamyb10-5R1 since Tamyb10-D1 gene in white-grained wheat varieties might be deleted. (Himi et al., 2011). Therefore, Wilcoxon rank sum test of two genotypes (0, 1) in the advanced backcross population was performed, revealing significant differences (p < 0.01) in seed dormancy between the two genotypes. This result implied that Tamyb10-D1 gene may have prominent correlation with seed dormancy in the advanced backcross population.
Figure 5. PCR amplification of TaVp1 and Tamyb10 sites in partial strains: TaVp1 (A) (M: DL2000 marker; 1: Ae. tauschii (282 bp); 2: Zhoumai 18 (423 bp); 3–13: partial strains of advanced backcross population.); Tamyb10 (B) (M: DL2000 marker; 1: Ae. tauschii (389 bp); 2: Zhoumai 18; 3–11: partial strains of advanced backcross population).
Discussion
Exploration and utilization of fine genes from Ae. tauschii is an effective approach to improve the resistance of common wheat, especially in view of the drastic reduction in genetic diversity due to modern breeding (Sukhwinder et al., 2012). Meanwhile, it is convenient to transfer Ae. tauschii genes into common wheat by recombination between homologous chromosomes, and most possibly, undesirable gene linkages could be easily broken by repeated backcross with common wheat. Direct crossing from diploid species into hexaploid wheat has been applied as a possible plant breeding technique for rapid introgression of useful traits. Gill and Raupp (1987) provided the first systematic direct gene transfer protocol. Based on this perspective, BC2F1 population was constructed through direct crossing of Ug99-resistant Ae. tauschii with rust-susceptible wheat (Olson et al., 2013). Another work of direct crossing was reported by Sehgal et al. (2011), who constructed BC1F4 population derived from the cross of three heat-tolerant Ae. tauschii with bread wheat. In this work, advanced backcross population of BC3F4 was constructed through synthetic octaploid wheat as a “bridge,” which was obtained from chromosome doubling of hybrid F1 through direct crossing of Ae. tauschii T093 with common wheat Zhoumai 18. Meanwhile, many strains with poor comprehensive traits could be eliminated in the process of multigenerational backcross and selfing. Therefore, only 27.8% SSR markers were detected in the advanced backcross population, though 374 SSR markers between Ae. tauschii accession T093 and Zhoumai 18 were determined to be polymorphic. While in another aspect, the reserved strains may possess better agronomic traits, and no phenotype segregation was found in each line, indicating that these lines are cytogenetically stable, which could be utilized more easily through further breeding.
Seed dormancy is widely regarded as one of the most critical factors for PHS resistance in common wheat, which is greatly influenced by temperature in seed germination stage. Specially, high temperature (>26°C) has negative influence on seed dormancy in late development stage (Ueno, 2002). In this work, the experiment was conducted at ~25°C, very close to that proposed in the previous literature (Ueno, 2002). The strains with high Dor values could still be detected in this case, revealing the strong additive effect of QTL for seed dormancy in the advanced backcross population. These strains containing desirable seed dormancy characterization herein could provide valuable genes for PHS-resistance breeding.
It is well known that wheat grain color (GC) is linked to PHS-resistance, and red-grained wheat is of more PHS resistance than the white-grained one (Flintham, 2000; Warner et al., 2000; Himi et al., 2002). Early cytogenetic study suggested that GC was controlled by three genes, R-A1, R-B1, and R-D1, locating on homoeologous group 3 chromosomes (Metzger and Silbaugh, 1970). Groos et al. (2002) detected 3 QTLs for PHS locating on the long arm of chromosomes 3A, 3B, and 3D in a bi-parental population, closing to the loci of genes R and TaVp1, with boundary from Xgwm314 to Xcfd9 on chromosome 3D and marker interval of 37.9 cM. The additive effect of QTLs was attributed to the wheat variety “‘Renan” with red kernels. Lin et al. (2016) also found 3 QTLs for GC on chromosome 3A, 3B, and 3D in 185 wheat cultivars by genome-wide association study (GWAS). Among the 3 sites, Tamyb10-D1 demonstrated the highest effect on GC (R2 = 0.23) in the association mapping panel. Moreover, the corresponding Qphs.hwwgr-3DL for PHS-resistance was also observed on chromosome 3D, explaining PVE of 8.3%, which suggests the pleiotropic effects of Tamyb10-D1 on PHS resistance under the field conditions. In this study, the additive effect of QDor-3D origins from Ae. tauschii, with the highest value of 20.91 and PVE of 13.83% (higher than the PVE of Qphs.hwwgr-3DL). Further analysis indicates that Tamyb10-D1 from Ae. tauschii is highly related with seed dormancy (p < 0.01), while no correlation was found between TaVp1 and seed dormancy. A novel candidate gene is thus speculated to exist between QDor-3D (576.5 Mb) and Tamyb10-D1 (583.9 Mb) for rather large distance (7.4 Mb) in physical position and the little difference in testa color (yellow) among the lines.
QTLs for PHS on chromosome 2D have been identified in recent years. Through a DH population from cross of wheat Cascades with AUS1408, Tan et al. (2006) found a major QTL locating on chromosome 2D (marker interval Xwmc112-Xgwm102), with enhanced dormancy from the allele of Cascades. Ren et al. (2008) detected a major QTL (Qphs.sau-2D) for PHS-resistance on the short arm of chromosome 2D in 140 F2 plants. The Qphs.sau-2D was identified within the marker interval of Xwmc261-Xgwm484, with genetic distance of 15.4 cM, whose additive effect was established to be derived from the D genome of synthetic hexaploid wheat cultivar “RSP.” In this study, the additive effect of QDor-2D originates from Ae. tauschii, with the highest value of 25.19 and PVE of 20.40 %, which was located on Xwmc503 of 2D, which was completely included in Xgwm261-Xgwm484 based on the Ae. tauschii reference genome. Specifically, the physical positions of Xwmc503 and Xgwm261 are respectively located in 22226966 ~ 22227188 bp and 22218627 ~ 22218480 bp, with a strikingly close distance of 8 Kb. QTLs for PHS-resistance could be found at analogous positions on 2D by utilizing different mapping populations, providing a strong evidence of the existence of candidate genes for PHS-resistance nearby. From this point of view, the QDor-2D identified in this study is suitable for marker-assisted breeding to trace the Ae. tauschii segment with seed dormancy characterization.
In conclusion, an advanced backcross population containing only Ae. tauschii segments was established through the synthetic octaploid wheat (hexaploid wheat Zhoumai 18 × Ae. tauschii T093) as a “bridge.” Meanwhile, 2 major QTLs (QDor-2D and QDor-3D) for seed dormancy from Ae. tauschii were located on Xwmc503 of 2D and Xcfd223 of 3D through the advanced backcross population, respectively. These QTLs could provide valuable information for marker-assisted breeding, and the obtained strains with long seed dormancy may also provide novel genetic resource for PHS-resistance in wheat breeding.
Author Contributions
Conceived and designed the study: LS. Generated the data and performed the analysis: ZD, HJ, HL, ZC, and LS. Contributed reagents, materials, analysis tools: ZY and SY. Wrote the paper: ZD and LS. All authors read and approved the final manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
This work was supported by National Natural Science Foundation of China (Grant Nos. 31401379, 31571649 and 31601297) and Project of Young Teachers in Henan Province (Grant No. 2015GGJS-019) and Project of Major Science and Technology in Henan Province (Grant No. 161100110400), and Project of Science and Technology Department of Henan Province (Grant No. 1721021100048).
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2017.02123/full#supplementary-material
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Keywords: quantitative trait locus (QTL), Aegilops tauschii, pre-harvest sprouting, seed dormancy, synthetic octaploid wheat
Citation: Dale Z, Jie H, Luyu H, Cancan Z, Yun Z, Yarui S and Suoping L (2017) An Advanced Backcross Population through Synthetic Octaploid Wheat as a “Bridge”: Development and QTL Detection for Seed Dormancy. Front. Plant Sci. 8:2123. doi: 10.3389/fpls.2017.02123
Received: 12 October 2017; Accepted: 29 November 2017;
Published: 13 December 2017.
Edited by:
Jose Maria Barrero, Commonwealth Scientific and Industrial Research Organisation (CSIRO), AustraliaReviewed by:
Marion S. Röder, Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK), GermanyJirui Wang, Sichuan Agricultural University, China
Copyright © 2017 Dale, Jie, Luyu, Cancan, Yun, Yarui and Suoping. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Li Suoping, hedawheat@163.com; lisuoping@henu.edu.cn
†These authors have contributed equally to this work.