Figures
Abstract
The development of alien addition lines is important for transferring useful genes from exotic species into common wheat. A hybrid of common wheat cv. 7182 (2n = 6x = 42, AABBDD) and Psathyrostachys huashanica Keng (2n = 2x = 14, NsNs) via embryo culture produced the novel intergeneric disomic addition line 59-11. The seed morphology of 59-11 resembled the parent 7182 and it exhibited extreme agronomic characteristics, i.e., twin stable spikelets, fertile florets, and multi-kernel clusters. Furthermore, 59-11 produced plump kernels with a high seed-setting percentage during the advanced maturation stage. The line was screened based on genomic in situ hybridization, EST-SSR, EST-STS, and gliadin to identify P. huashanica chromatin in the wheat background. The chromosome number and configuration of 59-11 was 2n = 44 = 22 II and we confirmed the 6Ns disomic chromosome additions based on A-PAGE analysis and molecular markers. The results suggested that the production of twin spikelets and multiple kernels per spike in the wheat-P. huashanica addition line was related to homologous group 6 in the wheat chromosome. This is the first report of the introduction of improved spike traits into common wheat from the alien species P. huashanica and it opens up the possibility of increasing the wheat yield based on this enlarged gene pool.
Citation: Du W, Wang J, Pang Y, Li Y, Chen X, Zhao J, et al. (2013) Isolation and Characterization of a Psathyrostachys huashanica Keng 6Ns Chromosome Addition in Common Wheat. PLoS ONE 8(1): e53921. https://doi.org/10.1371/journal.pone.0053921
Editor: Khalil Kashkush, Ben-Gurion University, Israel
Received: September 6, 2012; Accepted: December 4, 2012; Published: January 10, 2013
Copyright: © 2013 Du 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: The funds of the Ministry of Science and Technology of the People's Repubilc of China (No.2011AA10010203) and Northwest A&F University (No.Z109021002, A212020716), which only provide funds for purchases equipments and reagents. The funders had no other 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.
Introduction
The enrichment of wheat (Triticum aestivum) cultivars requires the continuous supply of new genetic variation [1]. The wild relatives of common wheat have been used for this purpose since the last century. Many genes that confer exceptional traits have been introduced into wheat by wide hybridization [2], [3], [4]. A rapid and effective method applied during the transfer process is the production of a tertiary gene pool, such as an addition line. Indeed, the production of alien addition lines is an important step during successful gene transfer to wheat because it plays a bridging role in the creation of alien substitution lines and translocation lines. Useful traits have been introduced successfully from wild relatives, including Thinopyrum elongatum [5], Secale cereale L. [6], Leymus racemosus [7], and Hordeum chilense [8], into hexaploid wheat via the development of alien addition lines.
Psathyrostachys huashanica Keng (2n = 2x = 14, NsNs) is a perennial cross-pollinating plant (subfamily Pooideae, tribe Triticeae, family Poaceae), which is generally found on the residual soil of mountainous braes and rocky slopes in the Huashan Mountains, Shaanxi Province, China [9], [10], [11]. It is characterized by early maturity and a high resistance to biotic (scab, stripe rust, take-all, and powdery mildew) and abiotic (cold, salinity, drought, and barren conditions) stresses [11], [12], [13], [14], [15], [16], [17]. P. huashanica Keng is also an important germplasm resource used for research into the floristic composition, origin, evolution, and breeding of Triticum spp.
Our research team successfully produced a heptaploid hybrid H8911 of common wheat and P. huashanica via embryo culture and back-crossing [12]. After a second back-crossing and one generation of selfing, we then developed a batch of wheat-P. huashanica monosomic addition lines [13]. Extensive studies of P. huashanica have also produced intergeneric amphiploids [14], [16], disomic addition lines [17], a 1 Ns addition line [15], a 3 Ns addition line [18], and disomic and monosomic addition lines [19]. However, there are no reports of 6 Ns alien disomic addition lines. The objectives of the current study were: (a) to identify the alien chromosome in wheat lines derived from crosses with P. huashanica using EST-SSR, EST-STS, and gliadin analyses; and (b) to describe and map the characteristic ‘twin spikelets’ derived from P. huashanica.
Results
Spike Traits of the Progeny Line Derived from Wheat-Psathyrostachys huashanica
The progeny line 59-11 derived from a cross between common wheat cv. 7182 and P. huashanica had interesting morphotypes, i.e., a stable genetic character with twin spikelets, and multiple florets and kernels. The twin spikelets emerged in the lower middle position of a spike and the total grain number per twin spikelet was >7. The spikes of the 59-11 plants were equipped with small tip awns and they were located in a similar position to that in P. huashanica, which distinguished them from the full awn of the female parent 7182. The 59-11 spikes were bulkier than the spikes of its parents. In addition, 59-11 produced plump red seeds that were similar to those produced by the female parent 7182 and they had a higher 1000-kernel weight (about 48 g) (Fig. 1). The plant height of 59-11 was lower than that of its parents, wheat cv. 7182 and P. huashanica. Ten plants were used to determine the mean height of 59-11 and they contained 150 tillers with an average of 15 tillers per plant, while we also analyzed the length, kernels, and spikelet numbers of 150 spikes. The Student’s t test showed that the 59-11 was significantly different from its parents, wheat cv. 7182 and P. huashanica (P<0.01 and P<0.05) in terms of the plant height, kernels per spike, and 1000-kernel weight (Table 1).
adult plants; b spikes; c spikelets and seeds. 1 7182, 2 Psathyrostachys huashanica, 3 59-11.
Cytological Characterization of Wheat-P. huashanica Disomic Addition Lines
The hybrid H881 (2n = 28, ABDNs) derived from 7182 and P. huashanica was successfully produced by embryo culture in 1991 and spontaneous chromosomal doubling via backcrossing, which was conducted to generate the heptaploid hybrid H8911 (2n = 49, AABBDDNs). Further backcrossing produced a batch of wheat-P. huashanica monosomic addition lines. One of these, 59-11, was found to have a chromosome configuration of 2n = 43 based on cytogenetic and GISH analyses, while it also possessed the specific A-PAGE band of P. huashanica and a twin spikelet morphology. Continuous strict, single-selfing generations were conducted, which were also accompanied by cytology, GISH screening, A-PAGE analyses, and morphological observation. Twenty BC2F2 plants having a chromosome number of 2n = 44 and twin spikelets with multiple florets and kernels were selected (Fig. 2a). We examined the chromosome pairing behavior of these plants in the PMCs during metaphase I. Twenty-two bivalents were found in 93% of the PMCs (Fig. 2b). The progeny line had an average of 0.76 univalents, 18.09 ring bivalents, and 3.15 rod bivalents. No trivalents or quadrivalents were observed (Table 2). These results suggested that the exotic P. huashanica chromosome had a high inheritability ratio during the selection of the addition line. Thus, P. huashanica chromosomes can be transmitted stably in a wheat background. Finally, we developed the wheat-P. huashanica disomic addition line 59-11 with twin spikelets, and multiple florets and kernels.
a Somatic chromosomes in root tips, 2n = 44; b Chromosome behavior of PMCs at metaphase I, 2n = 22 II.
GISH Analysis of the Wheat-P. huashanica Progeny Line
GISH was used to analyze the chromosome configuration and composition of 59-11. The total genomic P. huashanica DNA was used as a probe with Chinese Spring as the blocking DNA. Mitotic GISH showed that the root tip cells of 59-11 contained two chromosomes with strong yellowish-green hybridization signals (Fig. 3a). Meiotic GISH indicated that the metaphase I PMCs also had one ring bivalent yellowish-green signal (Fig. 3b). This suggested that 59-11 contained two chromosomes from different genomes in a wheat background. The two alien chromosomes could form bivalents and they were processed normally during synapsis, pairing, and segregation. These results also confirmed that 59-11 was a P. huashanica disomic addition line, which contained 42 wheat chromosomes and a pair of P. huashanica chromosomes.
a Somatic metaphase of the disomic chromosome addition line with two Psathyrostachys huashanica chromosomes (yellowish-green color); b PMCs at meiotic metaphase I, where the yellowish-green color indicates a ring bivalent chromosome from Psathyrostachys huashanica (color figure online).
Characterization with EST-SSR and EST-STS Markers
EST-SSRs and EST-STS markers were used to determine the homoeologous relationships between the added P. huashanica chromosomes and wheat. We screened 46 EST-SSRs primer pairs in the parents, which were distributed on different chromosome groups in wheat. We found that 40 pairs (87%) had amplified polymorphism bands. However, when these primers were used to analyze the disomic wheat-P. huashanica line 59-11, only one EST-SSR, SWES2, which was located on 6A, 6B, and 6DS, produced the specific bands in P. huashanica and 59-11 (Fig. 4a; Table 3). This suggests that the pair of alien P. huashanica chromosomes transferred into common wheat were associated with the sixth group of wheat chromosomes.
a SWES2 and b CD452568 amplified specific bands in the addition line in chromosomes 6A, 6B, and 6DS, and, 6AL, 6BL, and 6DL, respectively (arrows). M marker, 1 Psathyrostachys huashanica, 2 7182, 3 chromosome addition line 59-11. Arrows indicate the diagnostic amplification products of Psathyrostachys huashanica.
We used 200 EST-STS primer pairs related to seven groups of wheat chromosomes to gain further insights into 59-11. One EST-STS primer, CD452568, that mapped onto 6AL, 6BL, and 6DL, amplified the allele-specific bands of P. huashanica in the disomic addition line 59-11(Fig. 4b; Table 3). These results confirmed that the two P. huashanica chromosomes in addition line 59-11 were homoeologous to the sixth chromosome group in wheat.
Gliadin Analysis
A-PAGE was used to separate gliadin proteins from the P. huashanica and chromosome disomic addition line 59-11. One band that was specific to P. huashanica in the α-gliadin section, based on its mobility, was also detected in 59-11 (Fig. 5). It was clear that 59-11 had the same banding patterns as common wheat 7182, while it also contained a specific α-gliadin band from P. huashanica. Given that the encoded α-gliadin genes mapped onto the short wheat chromosome arm of group 6, the specific P. huashanica α-gliadin band further confirmed that the P. huashanica chromosome in 59-11 was correlated with the sixth group of the wheat chromosome.
1 7182, 2 Psathyrostachys huashanica, 3 59-11. The arrow shows specific bands from Psathyrostachys huashanica that appeared as α-gliadin in 59-11.
Discussion
Identification of P. huashanica Chromosomes in the Addition Line
GISH is the most efficient and accurate technique for tracking alien chromosomes or smaller fragments of different genomes in allopolyploids and wide hybrids [20]. GISH was employed to identify the chromosomal configuration and composition of the 59-11 line with exceptional spikelet characteristics during the mitotic and meiotic phases, using P. huashanica as a probe and Chinese Spring as a blocker. The results showed that the progeny line was a wheat-P. huashanica disomic addition line (Fig. 3). We tested the segregation of the P. huashanica chromosome in the progeny line 59-11 and we found that the desirable spike characteristics had a close relationship a pair of P. huashanica chromosomes. The wheat-P. huashanica addition line from 59-11 was also shown to be homologous to the group 6 wheat chromosome based on EST-SSR, EST-STS, and A-PAGE analysis (Fig. 4; Fig. 5). It was clear that the chromosomes derived from P. huashanica were the main cause of the increased spikelet number and multiple kernels per spike, and the chromosomes were assigned as 6Ns. This is the first report of a useful and effective agronomic trait involved with enhanced floret and kernel number being produced in a common wheat background via the transfer of chromatins from the alien species P. huashanica. This wheat-P. huashanica disomic addition line with exceptional agronomic traits could provide fresh germplasm for wheat yield improvement.
The EST regions, including intron sequences, could also be used as accurate anchor markers of genomic relationships when comparing the homoeologous chromosome regions [21]. Furthermore, EST-SSR and EST-STS markers have been used extensively as effective tools for the genetic analysis of alien chromosomes. The alien chromatin of wheat-A. cristatum addition and substitution lines were designated as 6P based on EST-SSR analysis [22]. An alien fragment on 2DL in a wheat-Thinopyrum substitution line was detected by EST-STS [23]. Two sets of EST-SSR markers were used to identify the sub-arm of prolamin loci on the 1Hch chromosome in a wheat background [8]. One EST-SSR marker and one EST-STS marker in wheat homoeologous group 6 identified polymorphism differences between wheat and P. huashanica, suggesting that these loci were physically located in similar homoeologous positions in P. huashanica and its progeny line. In addition, A-PAGE was used to determine the homoeologous group and genome affinity of the added chromosomes.
Many novel storage protein genes have been found in genera that are genetically close to wheat, e.g., P. huashanica [14], [15], Th. intermedium ssp. trichophorum [24], and C. delieana [25]. We found that the disomic addition line 59-11 had a specific band from P. huashanica in the α-gliadin section based on gliadin analysis (Fig. 5). The α- and β-gliadins are encoded by the short arm of group 6 in wheat, so it was inferred that the 59-11 alien disomic addition line carried the group 6 homoeology chromosome 6Ns from P. huashanica. Thus, the gliadin band of P. huashanica can be used as genetic marker to detect the corresponding chromosomes regions during gene transfers to wheat. It was concluded that the alien disomic addition line carried the group 6 homoeology chromosome 6Ns from P. huashanica based on a combination of EST-SSR, EST-STS, and A-PAGE analysis. These primers and bands could be used as simple and convenient markers for tracing P. huashanica 6Ns in a wheat background.
Potential Value of Twin Spikelets with Greater Numbers of Florets and Grains
The wheat yield could be improved by increasing the wheat grain number per unit area and per spike, and there is a growing interest in increasing the spikelet number per spike [26]. This superior spike trait could be useful for improving the yield of wheat and it can be achieved by the introgression of chromosomes from wild relatives of wheat, e.g., Secale cereale L. [27], [28] and Hordeum chilense [29]. In the current study, the addition line 59-11 was identified as a 6Ns chromosome addition line, which produced twin spikelets and an average of ten twin spikelets per spike. 59-11 was characterized by fertile florets, multiple kernels, a more advanced mature stage, plump kernels, and an optimum combination of tiller number and high seed-setting percentage, which possibly makes it optimal for high-yield breeding (Table 1, Fig. 1).
In summary, we found that gene(s) controlling the twin spikelets per spike characteristic of the wheat-P. huashanica progeny line were located on the 6Ns chromosome. Chromosome 6D was active in improving the floret number per spike by increasing the spikelet number within a spike [30]. Wheat-A. cristatum chromosome addition lines and substitution lines related to 6P also have more florets and kernels within a spike [22]. P. huashanica, as a tertiary gene pool, has homologous genomes with common wheat [31]. It is possible that the exceptional characteristics of the spike could be enhanced further by doubling the genes or accumulating genes in the group 6 loci. Ongoing research will be needed to monitor the association between the different arms of 6Ns and the exceptional spike trait to locate and/or map this trait onto specific chromosome regions. This novel addition line provides a solid foundation for the introgression of critical genes/QTLs from 6Ns into wheat.
A combination of GISH, EST-SSR, EST-STS, gliadin, and morphological analyses clearly identified the presence of the P. huashanica chromosome 6Ns in a wheat background, where it was responsible for the production of twin spikelets per spike in wheat. The results of this study may be important for further elucidating the structure and function of the P. huashanica 6Ns chromosome in a wheat background, while it also provides fresh insights into the evolutionary divergence of P. huashanica chromosomes from its cereal relatives.
Materials and Methods
Plant Materials
Wheat cv. 7182 (2n = 42, AABBDD), P. huashanica (2n = 14, NsNs), and the progeny of 59-11 (2n = 44) were used in this study. The parents 7182 and P. huashanica were included as controls to assess the spike traits and for EST-SSR, EST-STS, and gliadin analysis. Chinese Spring was used as a source of blocking DNA in the genomic in situ hybridization (GISH) analysis. These plant materials are deposited at the Shaanxi Key Laboratory of Genetic Engineering for Plant Breeding, College of Agronomy, Northwest A&F University, Shaanxi, China.
Evaluation of Spike Traits
The association of P. huashanica chromosomes with twin spikelets was evaluated during the 2009, 2010, and 2011 field harvest seasons in Yangling, Shaanxi, China (N 34°16′ 56.24′′, E 108°4′ 27.95′′). This area has fertile soil and a temperate continental monsoon climate, with an elevation of 530.1–403.2 m, and the annual average temperature, sunshine, and precipitation are 12.9°C, 2196 h, and 660 mm, respectively. Plants were arranged separately in a randomized complete block design using two replicates. Ten randomly selected 59-11 plants to assess the yield-related traits such as tillering, spike length, kernel number per spike, the number of spikelets, number of seeds per spikelet, the 1,000-kernel weight, awn length and plant height. The Student’s t test was used to test for significant differences between 59-11 and its parents, wheat cv. 7182 and P. huashanica, for all traits, except for the spikelets per twin spikelet and the kernels per twin spikelet.
Cytogenetic Analysis
Seeds were germinated in Petri dishes at 23°C in the dark until the roots reached 1–2 cm in length. Roots were excised from geminated seeds and incubated in ice-cold water overnight, and fixed in Carnoy’s solution with 95% ethanol-acetic acid (3∶1, v/v). Pollen mother cells (PMCs) were collected from young panicles and fixed in absolute ethanol-chloroform-glacial acetic acid (6∶3:1, v/v). Mitotic and meiotic chromosomes were squashed on a slide in a drop of acetocarmine and 45% acetic acid, and then used for cytological observation and GISH, respectively. The cover slips were removed after freezing the slides with liquid nitrogen, followed by air-drying and storage at –20°C.
GISH Analysis
The total genomic DNA was extracted from the fresh leaves of P. huashanica using the modified CTAB method [32]. The P. huashanica probe DNA was labeled with digoxigenin (digoxigenin-11-dUTP, Roche, Germany) via the nick-translation method. In situ hybridization was performed as previously described [33]. The slides were treated with RNase A (2 µg/ml in ddH2O) for 1 h at 37°C. The 40 µl hybridization solution contained 1 µl 10% (W/V) SDS, 1 µl ssDNA (salmon sperm DNA, 5 ug/µl), 20 µl formamide, 4 µl 20× SSC, 8 µl 50% (W/V) dextran sulfate, 100 ng probe DNA, and 3 µl ddH2O, and it was denatured by boiling for 10 min, before cooling in ice for 10 min. The denatured hybridization mixture was applied to each slide and allowed to hybridize overnight in a humid chamber at 37°C. Two post-hybridization washes of 2× SSC at 37°C were applied for 3 min each, followed by 3 min washes at room temperature. We added 50 µl FITC coupled to anti-dig antibody to detect and visualize the labeled chromosomes, while propidium iodide (PI) was added to stain unlabeled chromosomes. Fluorescent signals were viewed and photographed (Olympus BX60) with a Photometrics SenSys CCD camera.
EST-SSR and EST-STS Molecular Analysis
Genomic DNA was isolated from the wheat-P. huashanica addition line and both parents, as previously described [32]. To characterize the genomic composition of the wheat-P. huashanica addition line, we used 46 EST-SSR and 200 EST-STS multiple-loci primer pairs that were derived from a previous report [34] and (http://wheat.pw.usda.gov/SNP/new/pcr_primers.shtml), respectively, which were located on seven wheat homoeologous groups. Twenty microliters of each reaction mixture contained 2 µl 10× PCR buffer, 2 µl primer (2.5 µmol/ml), 2 µl DNA template (40–60 ng/µl), 1.6 µl dNTPs (2.5 µmol/ml), 1.6 µl MgCl2 (2.5 mmol/ml), 0.1 µl Taq polymerase (5 U/µl), and 10.7 µl ddH2O. The amplification procedure consisted of initial denaturation for 3 min at 94°C, followed by 35 cycles of 1 min at 94°C, 50 s at 60°C, and 1 min at 72°C, with a final extension for 10 min at 72°C. The PCR products were separated under standard conditions on 8% non-denatured polyacrylamide gel electrophoresis (PAGE) gels and visualized by silver staining.
Prolamin Extraction and Electrophoretic Analysis
Seed proteins were extracted from the crushed endosperms of single kernels. Acid polyacrylamide gel electrophoresis (A-PAGE) was conducted to fractionate gliadin proteins using a previously described method [15]. The extraction buffer contained 25% (v/v) 2-chloroethanol and 0.05% (w/v) methyl green, and the separations were conducted using standard A-PAGE at pH 3.1 with low catalyst (ferrous sulfate and hydrogen peroxide) levels to increase the gel firmness. Electrophoresis was carried out at 20 mA/gel at 10°C. The gels were fixed with 15% (w/v) trichloroacetic acid solution for 30 min, then stained overnight with 0.1% (w/v) Coomassie Brilliant Blue R-250 dissolved in absolute ethanol. De-staining was performed with tap water.
Acknowledgments
The authors would like to thank Dr Duncan E. Jackson for useful advice and English language editing of the manuscript.
Author Contributions
Carried out hybrid of common wheat cv. 7182 (2n = 6x = 42, AABBDD) and Psathyrostachys huashanica Keng (2n = 2x = 14, NsNs) via embryo culture: QY. Conceived and designed the experiments: WD J. Wu. Performed the experiments: WD J. Wang YP YL XC. Analyzed the data: JZ QY. Contributed reagents/materials/analysis tools: YP XC JZ QY. Wrote the paper: WD.
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