Figures
Abstract
The strategies of crossing B. napus with parental species play important role in broadening and improving the genetic basis of B. napus by the introgression of genetic resources from parental species. With these strategies, it is easy to select new types of B. napus, but difficult to select new types of B. rapa or B. oleracea by self-pollination. This characteristic may be a consequence of high competition with B. napus gametes. To verify the role of gamete viability in producing new B. napus individuals, the meiotic chromosome behavior of the interspecific hybrid between B. napus (Zhongshuang 9) and B. oleracea (6m08) was studied, and microspore-derived (MD) individuals were analyzed. The highest fitness of the 9:19 (1.10%) pattern was observed with a 5.49-fold higher than theoretical expectation among the six chromosome segregation patterns in the hybrid. A total of 43 MD lines with more than 14 chromosomes were developed from the hybrid, and 8 (18.6%) of them were B. napus-like (n = 19) type gametes, having the potential to broaden the genetic basis of natural B. napus (GD = 0.43 ± 0.04). It is easy to produce B. napus-like gametes with 19 chromosomes, and these gametes showed high fitness and competition in the microspore-derived lines, suggesting it might be easy to select new types of B. napus from the interspecific hybrid between B. napus and B. oleracea.
Citation: Li Q, Chen Y, Yue F, Qian W, Song H (2018) Microspore culture reveals high fitness of B. napus-like gametes in an interspecific hybrid between Brassica napus and B. oleracea. PLoS ONE 13(3): e0193548. https://doi.org/10.1371/journal.pone.0193548
Editor: Yong Pyo Lim, Chungnam National University, REPUBLIC OF KOREA
Received: December 17, 2017; Accepted: February 13, 2018; Published: March 1, 2018
Copyright: © 2018 Li 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.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by the National Key Research and Development Program of China (2017YFD0101804), Hongyuan Song receive the funding; the China Postdoctoral Science Foundation (2015M582500) and the Fundamental Research Funds for the Central Universities in China (XDJK2016C080), the Chongqing Postdoctoral Science Foundation (Xm2016029), Qinfei Li receive these three funding; the Science and Technology Innovation Project of Chongqing (cstc2015shms-ztzx80005, cstc2015shms-ztzx80007 and cstc2015shms-ztzx80009), Hongyuan Song receive these fundings. 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.
Introduction
Brassica oleracea is an important vegetable crop and is genetically diverse, having various subspecies, such as cabbage, cauliflower, broccoli, kale and wild-type, and having many known useful traits, such as its strong resistance against Sclerotinia incorporated from wild subspecies of B. incana [1, 2]. B. napus is an important oilseed crop in the world, originating from a natural interspecific hybridization between B. rapa and B. oleracea ~6000 years ago [3, 4]. This crop’s genetic basis was narrower than the parental species due to its short history and domestication through modern breeding methods [5]. Introgression of genetic resources from parental species into B. napus is necessary to broaden and improve its genetic basis [6–9].
To utilize the genetic resources of parental species, the strategy of crossing B. napus and its parental species is commonly used. In the strategy, it is easy to select new types of B. napus, either gaining useful traits from parental species [10, 11] or having the potential to broaden the genetic basis of natural B. napus [8, 12, 13]. However, it is difficult to select new types of B. oleracea/B. rapa individuals, which might due to higher competition of B. napus gametes than B. oleracea/B. rapa gametes. To verify this hypothesis, the meiotic behavior of interspecific hybrid between B. napus and B. oleracea and its microspore-derived (MD) individuals were analyzed.
Microspore culture is widely applied in Brassica species to produce double haploid (DH) individuals in germplasm collection, QTL mapping, genetic engineering and crop improvement [14–17]. This method is less commonly used in interspecific hybrids between Brassica species due to the difficulty in obtaining embryoids [18–20]. However, scientists have used the technique in interspecific hybrids to induce microspore-derived lines, aiming to study male meiotic behavior, since there is no selection pressure from females compared with self-pollination and backcrossing [21, 22]. In the present study, an interspecific hybrid between B. napus and B. oleracea was developed, and its meiotic behavior and gamete behavior in microspore-derived individuals were analyzed, showing that the B. napus-like gamete had high fitness and competition in the hybrid. This suggested that high viability of B. napus-like gametes might make it easy to select new types of B. napus from the interspecific hybrid between B. napus and its parental species by self-pollination.
Materials and methods
Plant materials
The interspecific hybrid ACC was developed from hybridization between B. napus ‘Zhongshuang 9’ and B. oleracea ‘6m08’ via embryo rescue and propagated on MS regeneration medium (MS + 3 mg/L 6-BA + 0.02 mg/L NAA) via tissue culture for microspore culture [23]. Morphology, fertility, chromosome number and genetic components of MD lines were evaluated, and their genetic diversity was compared with 34 natural B. napus and 42 B. oleracea (S1 Table).
Cytological observations
Chromosome number at mitotic metaphase.
To check the chromosome numbers of the ACC hybrid and MD progenies, the young ovaries were collected and pretreated with 2 mmol/L 8-hydroxyquinoline for three to four hours at room temperature and later fixed in Carnoy’s solution (Vethanol: Vacetic acid = 3:1) and stored at 4 °C. Mitotic observations were made according to the methods as described by Li et al. [24]. The ovaries at mitosis were hydrolyzed in 1 M HCl at 60 °C for 8 min and stained with 10% modified carbol fuchsin and observed under microscope.
Chromosome pairing and segregation at meiosis.
For meiotic analysis, buds were fixed in Carnoy’s solution for 24 h and then transferred into fresh mixture and stored at –20 °C for future use. Meiotic observations of pollen mother cells (PMCs) were made according to the methods of Li et al. [24]. The anthers at meiosis stage were hydrolyzed in 1 M HCl at 60 °C for 2 min, stained with 10% modified carbol fuchsin and observed under microscope. The chromosome pairing at metaphase I and chromosome segregation at anaphase I in PMCs were recorded.
Pollen fertility
Pollen fertility was determined by the percentage of pollen grains stained with 1% acetocarmine according to the method of Li [24]. Three flowers were counted from ACC hybrid and MD lines. More than 300 pollen grains were recorded for each line. Grains that were round and stained red were considered normal, whereas small and non-stained ones were considered dead pollen.
Microspore isolation
Microspore culture was performed by the method described by Lichter [25], with minor modifications. A total of 30 flower buds ranging in length from 2.5 to 3.5 mm from the ACC hybrid were selected and sterilized in 10% sodium hypochlorite solution for 15 min. The sterilized buds were then released with B5-13 medium. The solution along with the microspores were filtered through a 48-μm filter and transferred into a sterile 10 mL centrifuge tube, and the volume was adjusted to 8 mL with B5-13 media. The microspores were then centrifuged for 3 min at 1200 rpm, and the supernatant was discarded. B5-13 media was added to mix the microspores, and then they were centrifuged for 3 min at 1200 rpm again. The supernatant was discarded and microspores were re-suspended in 8 mL NLN-13 solution (NLN medium plus 13% sucrose in Millipore water, pH to 5.8).
The microspore suspension was divided into 4 Petri dishes with diameter of 70 mm, and 4 mL NLN-13 and 1 mL 10% activated charcoal were added into each Petri dish, which were later sealed with parafilm. The isolated microspores were incubated at 32 °C for 48 hours and then transferred into a 24 °C incubator for 20 days [26]. The plates were then put on a shaker (60 rpm) for embryo development. Three weeks later, young embryos were transferred into ½ MS medium for plant induction.
SSR marker analysis
Genomic DNA was isolated from young leaves using the CTAB method [27]. 30 MD lines randomly selected were genotyped with 34 natural B. napus and 42 B. oleracea using 35 sets of SSR primers (S2 Table). The SSR results were described by the absence (0) or presence (1) of a band.
The genetic distance (GD) between accessions X and Y was calculated using the formula, GDxy = 1 –Nxy / (Nx + Ny), where Nxy is the number of common bands shared by accession X and Y, and Nx and Ny are the total number of bands in accession X and Y, respectively [28]. The phylogenetic tree was constructed using the neighbor-joining method implemented by MEGA version 6 [29].
Statistical analysis
Analysis of variance (ANOVA), Pearson’s simple correlation coefficient and X2 test were calculated using the statistical package SAS version 8.0 [30].
Results
Development of interspecific hybrid between B. napus and B. oleracea
Immature embryos 7~10 days after pollinating with B. oleracea (6m08) pollen on the stigma of B. napus (Zhongshuang 9) were cultured on ½ MS medium via embryo rescue. Three weeks later, an interspecific hybrid was developed, sharing intermediate morphology between two parents and having lighter green leaf color than both parents (Fig 1A–1C). Its pollen fertility was 34.82%, which was lower than the parental species (Zhongshuang 9: 99.5%, 6m08: 96.4%), and its chromosome number was 28 in meiotic and mitotic cells (Fig 2A).
(A) Zhongshuang 9 seedling; (B) 6m06 seedling; (C) hybrid ACC seedling; (D-I) Seedling of microspore-derived lines from the hybrid between Zhongshuang 9 and 6m08.
(A) One cell of ACC with chromosome number 28; (B) One PMC of ACC with 9II + 10I; (C) One PMC of ACC with 10II + 8I; (D) One PMC of ACC with 9:19; (E) One PMC of ACC with 10:18; (F) One PMC of ACC with chromosome bridge; (G) One microspore-derived line with 18 chromosomes; (H) One microspore-derived line with 38 chromosomes; (I) One microspore-derived line with 52 chromosomes. Those marked with stars were bivalent.
Meiotic behavior of an interspecific hybrid between B. napus and B. oleracea
Different chromosome conformations, such as univalents, bivalents, trivalents and quatrivalents, were observed in pollen mother cells (PMCs) at metaphase I (MI) of the hybrid. The average chromosome association was 9.66I + 9.12II + 0.01III + 0.02IV in 170 PMCs at MI. In certain cases, the frequency of the pattern of 9II + 10I (84.71%) was higher than the pattern of 10II + 8I (12.84%) (Fig 2B and 2C). Despite the high frequency of chromosome segregations of 13:15 (36.81%), 12:16 (30.77%) and 14:14 (15.93%) patterns were observed in 182 PMCs at anaphase I (AI), the fitness of the 9:19 (1.10%) pattern was the highest among the 6 patterns observed with a 5.49-fold higher fitness than the theoretical expectation (Fig 2D and 2E). This finding suggested that there would be a high probability of producing B. oleracea/B. napus-like gametes (C/AC = 9:19). In certain cases, meiotic irregularities, such as chromosome bridges and lagging chromosomes, were observed during the first and second divisions in the hybrid (Fig 2F).
Development of microspore derived plants
In total, 115 embryoids (18.55%) were induced from 620 flower buds between late uninucleate stage and early binucleate stage (2.5~3.5mm flower bud) of the hybrid via microspore culture. Only 43 MD lines were obtained after transplanting these embryoids on ½ MS medium for plant-induction. All of these lines shared light green leaf color with the hybrid but had different number of leaf auricles, for example, the number of the leaf auricles ranged from 0 to 5 (Fig 1D–1I).
Pollen fertility and chromosome number of microspore-derived plants
Pollen fertility of the MD lines ranged from 0 to 98.89%, with an average of 49.42%. Fertility was significantly positively correlated with chromosome number (P = 0.0027, r = 0.70; S3 Table), suggesting that lines with more chromosomes had higher pollen fertility.
In the 43 MD individuals, diverse chromosome numbers were observed. With the exception of one individual having 66 chromosomes and one having more than 80 chromosomes, the chromosome number of the other 41 individuals ranged from 15 to 56. Of these individuals, 14 were haploid, and 29 were polyploid by natural chromosome doubling. In detail, five of them had 17 chromosomes, five had 38 chromosomes, four had 30 chromosomes, four had 56 chromosomes and three lines had 19 chromosomes. Overall, twelve patterns of gametes were found. The frequency of actual gametes was significantly different from the theoretical gametes via X2 test (P < 0.0001). This analysis showed that all the individuals had more than 14 chromosomes, suggesting that gametes having more chromosomes might survive, whereas the ones with less might die during the meiosis stage in the interspecific hybrid between B. napus and B. oleracea.
Although 27 (65.85%) individuals were aneuploid (n ≠ 19), five (12.20%) individuals were unreduced gametes (n = 28), individuals having gametes with 19 chromosomes (19.51%, 8/41) were the most common of all the patterns (Fig 2G–2I). This indicated that B. napus-like individuals having gametes with 19 chromsomes were more competitive than others in the hybrid between B. napus and B. oleracea.
Genetic diversity of microspore derived plants
To verify the genetic diversity of the MD population, 115 polymorphic loci were amplified by genotyping 30 MD individuals with 35 combinations of SSR primers. Compared to the parental species (Zhongshuang 9 and 6m08), the MD population shared on average ~53 loci (45.71 ± 1.11%) with both parental species, ~37 loci (32.26 ± 1.60%) with the single parent B. napus (Zhongshuang 9) and ~14 (12.09 ± 1.60%) with the single parent B. oleracea (6m08). However, these plants also had ~11 unique loci (9.94 ± 1.11%) distinct from both parents. The average genetic distance between the MD population and the B. oleracea parent (0.91 ± 0.07) was significantly farther than the B. napus parent (0.34 ± 0.05, P < 0.0001). Compared to Zhongshuang 9, the genetic distance of B. napus-like individuals (0.39 ± 0.07, P = 0.046) was significantly more distant than aneuploid (0.33 ± 0.04) and unreduced gametes (0.32 ± 0.02). This finding was similar to the distance between MD lines and 6m08 (B. napus-like individuals: 0.94 ± 0.09; aneuploid: 0.91 ± 0.07; unreduced gamete: 0.88 ± 0.05; Table 1), suggesting more genetic components from the B. napus parent than the B. oleracea parent were inherited by the MD individuals.
This finding was in accordance with the distance among MD population, natural B. napus and B. oleracea. In comparison with 34 B. napus and 42 B. oleracea subspecies, the average genetic distance between MD population and B. oleracea population (0.97 ± 0.37) was similar to that between B. napus and B. oleracea population (0.97 ± 0.33), but it was further than that between MD population and B. napus population (0.42 ± 0.17), suggesting the MD population is different from natural B. napus and B. oleracea, but close to B. napus. The obvious genetic differences among MD lines, B. napus population and B. oleracea population were also supported by the phylogenetic tree (Fig 3). Although the average genetic distance among B. napus-like individuals, aneuploid and unreduced gametes were similar, the genetic distance of B. napus-like individuals to the natural B. napus group (0.43 ± 0.04, P = 0.0091) was farther than that of aneuploid (0.39 ± 0.03) and unreduced gametes (0.38 ± 0.02; Table 1). This finding indicated that these B. napus-like individuals, having gametes with 19 chromosomes, had the potential to widen the genetic basis of B. napus.
Discussion
Meiotic behavior of Brassica interspecific hybrid revealed by microspore culture
Interspecific hybridization plays an important role in exchanging genetic components, widening and improving genetic resources in Brassica species. Although high frequency of euploids (new type B. napus) was observed in the interspecific hybrid between B. napus and parental species [8, 9, 20, 31, 32], aneuploid and unreduced gametes occurred frequently due to abnormal meiosis of interspecific hybrids [33–36]. In the present study, only 43 individuals were developed from the interspecific hybrid between B. napus and B. oleracea due to the difficulty in generating a large number of microspore-derived lines, and these individuals exhibited 19.51% euploid, 65.85% aneuploid and 12.20% unreduced gametes.
The frequency of aneuploid, euploid and unreduced gametes in the interspecific hybrid might be attributable to genotype-specific effects, such as sharing a common subgenome, or environmental factors, such as cold or fluctuating temperatures, plant nutrition, water stress and disease [37–42]. In the present study, the interspecific hybrid sharing a common C-subgenome from B. napus and B. oleracea, and produced high frequency of euploid (19.51% B. napus-like gametes), which was similar to the interspecific hybrid between B. napus and B. rapa sharing an A-subgenome [20]. It is necessary to investigate the genetic or developmental factors that may give rise to this apparent selection for the variation of gametes in the interspecific hybrid between B. napus and B. oleracea in the future.
Genetic variance of microspore derived lines
In interspecific hybridization, chromosomes of related species recombine and interact regularly, causing homoeolog expression bias, genomic dominance and genomic imprinting [43–45]. In the MD lines, the genetic distance was closer to the B. napus parent (0.34 ± 0.05) than the B. oleracea parent (0.91 ± 0.07), suggesting more genetic components of B. napus than B. oleracea were inherited into the MD population. This might be due to genomic dominance and genomic imprinting of the B. napus parent in the MD lines. Subgenome dominance is an important phenomenon in allopolyploids, it was also observed in the interspecific hybrids. For example, in the interspecific hybrids (wheat × Aegilops), C-subgenome nucleolar organizing regions loci are dominant [46]. In addition, the subgenome dominance occurred instantly following the hybridization [47]. This bias in gene expression must be investigated in exploring the mechanism of B. napus genomic dominance.
In the present study, all of the MD lines were different from the parental species, especially the B. napus-like individuals, which has the potential to broaden the genetic basis of natural B. napus. The other lines might be used to produce monosomic alien addition lines and nullisomic lines, which can be used as bridge to transfer desired genes from wild B. oleracea species into B. napus [48, 49]. The role of these novel MD plants in Brassica species improvement needs to be evaluated in the future.
Supporting information
S1 Table. Accessions of 34 natural B. napus and 42 B. oleracea used to analyze genetic diversity of microspore-derived lines derived from the hybrid between B. napus and B. oleracea.
https://doi.org/10.1371/journal.pone.0193548.s001
(XLSX)
S3 Table. Data from microspore-derived lines derived from interspecific hybrid between B. napus and B. oleracea relating to fertility, chromosome number and genetic variance.
https://doi.org/10.1371/journal.pone.0193548.s003
(XLSX)
Acknowledgments
This study was partly supported by the National Key Research and Development Program of China (2017YFD0101804), the China Postdoctoral Science Foundation (2015M582500), the Fundamental Research Funds for the Central Universities in China (XDJK2016C080), the Chongqing Postdoctoral Science Foundation (Xm2016029), and the Science and Technology Innovation Project of Chongqing (cstc2015shms-ztzx80005, cstc2015shms-ztzx80007 and cstc2015shms-ztzx80009).
References
- 1. Mei J, Li Q, Yang X, Qian L, Liu L, Yin J, et al. Genomic relationships between wild and cultivated Brassica oleracea L. with emphasis on the origination of cultivated crops. Genet Resour Crop Evol. 2010; 57:687–692
- 2. Mei J, Qian L, Disi JO, Yang X, Li Q, Li J, et al. Identification of resistant sources against Sclerotinia sclerotiorum in Brassica species with emphasis on B. oleracea. Euphytica. 2011; 177:393–399
- 3. Chalhoub B, Denoeud F, Liu S, Parkin IAP, Tang H, Wang X, et al. Early allopolyploid evolution in the pos-neolithic Brassica napus to oilseed genome. Science. 2014; 345:950
- 4. U N. Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization. Jpn J Bot. 1935; 7:389–452
- 5.
Liu H. The genetics and breeding of oilseed rape. China Agr Univ Press, Beijing. China. 2000.
- 6. Girke A, Schierholt A and Becker HC. Extending the rapeseed gene pool with resynthesized Brassica napus I: Genetic diversity. Genet Resour Crop Evol. 2012; 59:1441–1447
- 7. Li Q, Mei J, Zhang Y, Li J, Ge X, Li Z, et al. A large-scale introgression of genomic components of Brassica rapa into B. napus by bridge of hexaploid derived from hybridization between B. napus and B. oleracea. Theor Appl Genet. 2013; 126(8):2073–2080 pmid:23699961
- 8. Li Q, Zhou Q, Mei J, Zhang Y, Li J, Li Z, et al. Improvement of Brassica napus via interspecific hybridization between B. napus and B. oleracea. Mol Breeding. 2014; 34:1955–1963
- 9. Qian W, Chen X, Fu D, Zou J, Meng J. Intersubgenomic heterosis in seed yield potential observed in a new type of Brassica napus introgressed with partial Brassica rapa genome. Theor Appl Genet. 2005; 110:1187–1194 pmid:15806350
- 10. Mei J, Liu Y, Wei D, Wittkop B, Ding Y, Li Q, et al. Transfer of Sclerotinia resistance from wild relative of Brassica oleracea into Brassica napus using a hexaploidy step. Theor Appl Genet. 2015; 128:639–644 pmid:25628163
- 11. Rahman H, Bennet RA and Séguin-Swartz G. Broadening genetic diversity in Brassica napus canola: Development of canola-quality spring B. napus from B. napus × B. oleracea var. alboglabra interspecific crosses. Can J Plant Sci. 2015; 95:29–41
- 12. Lu C and Kato M. Fertilization fitness and relation to chromosome number in interspecific progeny between Brassica napus and B. rapa: A comparative study using natural and resynthesized B. napus. Breeding Sci. 2001; 51:73–81
- 13. Qian W, Meng J, Li M, Frauen M, Sass O, Noack J, et al. Introgression of genomic components from Chinese Brassica rapa contributes to widening the genetic diversity in rapeseed (B. napus L.), with emphasis on the evolution of Chinese rapeseed. Thero Appl Genet. 2006; 113:49–54
- 14.
Friedt W and Zarhloul MK. Haploids in the improvement of Crucifers. Springer Berlin Heidelberg. 2005; 56:191–213
- 15. Geng XX, Chen S, Astarini IA, Yan GJ, Tian E, Meng J, et al. Doubled haploids of novel trigenomic Brassica derived from various interspecific crosses. Plant Cell Tiss Organ Cult. 2013; 113(3):501–511
- 16. Shariatpanahi ME and Ahmadi B. Isolated microspore culture and its applications in plant breeding and genetics. Plant Tissue Culture: Propagation, Conservation and Crop Improvement. 2016; pp:487–507
- 17. Yang S, Chen S, Geng XX, Yan G, Li ZY, Meng JL, Cowling WA, Zhou WJ. The first genetic map of a synthesized allohexaploid Brassica with A, B and C genomes based on simple sequence repeat markers. Thero Appl Genet. 2016; 129:689–701
- 18. Ge XH and Li ZY. Extra divisions and nuclei fusions in microspores from Brassica allohexaploid (AABBCC) × Orychophragmus violaceus hybrids. Plant Cell Rep. 2006; 25(10):1075–1080 pmid:16733741
- 19. Wen J, Zeng X, Pu Y, Qi L, Li Z, Tu J, et al. Meiotic nondisjunction in resynethesized Brassica napus and generation of aneuploids through microspore culture and their characterization. Euphytica. 2010; 173:99–111
- 20. Zhou Y and Scarth R. Microspore culture of hybrids between Brassica napus and B. campestris. Acta Botanica Sinica. 1995; 37:848–855
- 21. Mason AS, Takahira J, Atri C, Samans B, Hayward A, Cowling WA, et al. Microspore culture reveals complex meiotic behavior in a trigenomic Brassica hybrid. BMC Plant Biology. 2015; 15(1):173
- 22. Nelson MN, Mason AS, Castello MC, Thomson L, Yan G, Cowling WA. Microspore culture preferentially selects unreduced (2n) gametes from an interspecific hybrid of Brassica napus L. × Brassica carinata Braun. Theor Appl Genet. 2009; 119(3):497–505 pmid:19436985
- 23. Wen J, Tu J, Li Z, Fu T, Ma C, Shen J. Improving ovary and embryo culture techniques for efficient resynthesis of Brassica napus from reciprocal crosses between yellow-seeded diploids B. rapa and B. oleracea. Euphytica. 2008; 162:81–89
- 24. Li Z, Liu HL and Luo P. Production and cytogenetics of intergeneric hybrids between Brassica napus and Orychophragmus violaceus. Theor Appl Genet. 1995; 91:131–136 pmid:24169678
- 25. Lichter R. Induction of haploid plants from isolated pollen of Brassica napus. Z Pflanzenphysiol. 1982; 105:427–434
- 26. Malik MR, Wang F, Dirpaul JM, Zhou N, Hammerlindl J, Keller W, et al. Isolation of an embryogenic line from non-embryogenic Brassica napus cv. Westar through microspore embryogenesis. J Exp Bot. 2008; 59(10):2857–2873 pmid:18552352
- 27. Murashige T and Skoog F. A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plantarum. 1962; 15(3):473–497
- 28. Nei M and Li WH. Mathematical model for studying genetic variation in terms of restriction endouncleases. Proc Natl Acad Sci. 1979; 76:5269–5273 pmid:291943
- 29. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol Biol Evol. 2013; 30(12):2725–2729 pmid:24132122
- 30.
SAS Institute Inc. SAS Technical Report. SAS statistics Software: changes and enhancements. Release V8. SAS Institute Inc., Cary, North Carolina. 1992
- 31. Ayotte R, Harney PM, Machado VS. The transfer of triazine resistance from Brassica napus L. to B. oleracea L. II. Morphology, fertility and cytology of the F1 hybrid. Euphytica. 1988; 37:189–197
- 32. Ayotte R, Harney PM, Machado VS. The transfer of triazine resistance from Brassica napus L. to B. oleracea L. III. First backcross to parental species. Euphytica. 1988b; 38:137–142.
- 33. Nelson MN, Mason AS, Castello M-C, Thomson L, Yan G, Cowling WA. Microspore culture preferentially selects unreduced (2n) gametes from an interspecific hybrid of Brassica napus L. × Brassica carinata Braun. Thero Appl Genet. 2009; 119:497–505
- 34. Ramsey J and Schemske DW. Pathways, mechanisms, and rates of polyploid formation in flowering plants. Annu Rev Ecol Syst. 1998; 29:467–501
- 35. Silkova OG, Shchapova AI, Shumny VK. Patterns of meiosis in ABDR amphihaploids depend on the specific type of univalent chromosome division. Euphytica. 2011; 178:415–426
- 36. Xiong ZY, Gaeta RT and Pires JC. Homoeologous shuffling and chromosome compensation maintain genome balance in resynthesized allopolyploid Brassica napus. P Natl Acad Sci USA. 2011; 108(19):7908–7913
- 37. De Storme N and Geelen D. Sexual polyploidization in plant-cytological mechanisms and molecular regulation. New Phytol. 2013; 198:670–684 pmid:23421646
- 38. Fakhri Z, Mirzaghaderi G, Ahmadian S, Mason AS. Unreduced gamete formation in wheat × Aegilops spp. hybrids is genotype specific and prevented by shared homologous subgenomes. Plant Cell Rep. 2016; 35:1143–1154 pmid:26883221
- 39. Schmidt A, Schmid MW, Grossniklaus U. Plant germiline formation: common concepts and developmental flexibility in sexual and asexual reproduction. Development. 2015; 142:229–241 pmid:25564620
- 40. Mason AS, Nelson M, Yan G, Cowling W. Production of viable male unreduced gametes in Brassica interspecific hybrids is genotype specific and stimulated by cold temperatures. BMC Plant Biol. 2011; 11:103 pmid:21663695
- 41. Younis A, Hwang Y-J and Lim K-B. Exploitation of induced 2n-gametes for plant breeding. Plant Cell Rep. 2014; 33:215–223 pmid:24311154
- 42. Sora D, Kron P and Husband BC. Genetic and environmental determinants of unreduced gamete prodution in Brassica napus, Sinapis arvensis and their hybrids. Heredity. 2016; 117:440–448 pmid:27577694
- 43. Bardil A, de Almeida JD, Combes MC, Lashermes P, Bertrand B. Genomic expression dominance in the natural allopolyploid Coffea arabica is massively affected by growth temperature. New Phytol. 2011; 192:760–774 pmid:21797880
- 44. Buggs RJ, Zhang L, Miles N, Tate JA, Gao L, Wei W, et al. Transcriptomic shock generates evolutionary novelty in a newly formed, natural allopolyploid plant. Curr Biol. 2011; 21:551–556 pmid:21419627
- 45. Combes MC, Cenci A, Baraille H, Bertrand B, Lashermes P. Homeologous gene expression in response to growing temperature in a recent allopolyploid (Coffea arabica L.). J Hered. 2012; 103:36–46 pmid:22039298
- 46. Mirzaghaderi G, Abdolmalaki Z, Zohouri M, Moradi Z, Mason AS. Dynamic nucleolar activity in wheat × Aegilops hybrids: evidence of C-genome dominance. Plant Cell Rep. 2017; 36(8):1277–1285 pmid:28456843
- 47. Edger PP, Smith R, McKain MR, Cooley AM, Vallejo-Marin M, Yuan Y, et al. Subgenome dominance in an interspecific hybrid, synthetic allopolyploid, and a 140-year old naturally estabilished neo-allopolyploid monkeyflower. Plant Cell. 2017; 19(9):2150–2167
- 48. Abdelrahman M, EI-Sayed M, Sato S, Hirakawa H, Ito S, Tanaka K, et al. RNA-sequencing-based transcriptome and biochemical analyses of steroidal saponin pathway in a complete set of Allium fistulosum-A. cepa monosomic addition lines. PloS One. 2017; 12(8):e0181784 pmid:28800607
- 49. An D, Zheng Q, Liu Q, Ma P, Zhang H, Li L, et al. Molecular cytogenetic identification of a new wheat-rye 6R chromosome disomic addition line with powdery mildew resistance. PloS One. 2015; 10(8):e0134534 pmid:26237413