- Research article
- Open Access
Addition of Manas barley chromosome arms to the hexaploid wheat genome
© The Author(s). 2016
- Received: 4 May 2016
- Accepted: 7 June 2016
- Published: 21 June 2016
Cultivated barley belongs to the tertiary genepool of hexaploid wheat. Genes of interest can be transferred from barley into wheat through wide hybridization. The application of wheat-barley introgression lines could provide an excellent tool for the transfer of earliness, favourable amino acid composition, biotic stress resistance, abiotic stress tolerance, or good tillering ability into wheat.
A set of 10 wheat-barley ditelosomic addition lines (2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 6HS, 6HL, 7HS and 7HL) was developed from the progenies of an Asakaze/Manas wheat-barley hybrid produced in Martonvásár, Hungary. The addition lines were selected from self-fertilized plants of the BC2F2-BC2F4 generations using genomic in situ hybridization (GISH) and were identified by fluorescence in situ hybridization (FISH) with repetitive DNA probes [HvT01, (GAA)7 and centromere-specific (AGGGAG)4 probes]. The cytogenetic identification was confirmed using barley arm-specific SSR and STS markers. The ditelosomic additions were propagated in the phytotron and in the field, and morphological parameters (plant height, tillering, length of the main spike, number of seeds/spike and seeds/plant, and spike characteristics) were described. In addition, the salt stress response of the ditelosomic additions was determined.
The six-rowed winter barley cultivar Manas is much better adapted to Central European environmental conditions than the two-rowed spring barley Betzes previously used in wheat-barley crosses. The production of wheat-barley ditelosomic addition lines has a wide range of applications both for breeding (transfer of useful genes to the recipient species) and for basic research (mapping of barley genes, genetic and evolutionary studies and heterologous expression of barley genes in the wheat background).
- Wheat-barley ditelosomic addition lines
- Genomic in situ hybridization
- Fluorescence in situ hybridization
- SSR and STS markers
- Morphological parameters
- Salt stress response
Attempts to hybridize wheat with barley were begun more than 100 years ago , but the first authentic hybrid was obtained much later by the Danish scientist Kruse , who used barley as the female parent [3–5]. The production of the reciprocal hybrid (with wheat as the female parent and barley as the male parent) is more difficult, but this kind of combination is now in the focus of research in this field because of the pistilloidy and male sterility observed in barley × wheat hybrids . The development of the first wheat × barley hybrids was followed by the production of wheat-barley disomic addition lines (2H, 3H, 4H, 5H, 6H and 7H), the first of which arose from crosses between Chinese Spring wheat and the spring barley Betzes . The success of wheat × barley crosses is very dependent on the genotypes used. Previous experience demonstrated that wheat cultivars originating from the Far East have better crossability with related species. Several barley cultivars (Betzes, Igri, Manas and Osnova) were used in wheat-barley crosses in Martonvásár . The Ukrainian six-rowed barley Manas has many useful agronomic characters (e.g. good winter hardiness, abiotic stress tolerance and yield ability) and is well adapted to Central European conditions .
The first and as yet only near complete set of hexaploid wheat-barley ditelosomic addition lines was produced by Islam in the 1980’s using a set of monosomic additions of Betzes barley (2n = 2× = 14; HH) chromosomes to hexaploid Chinese Spring wheat (2n = 6× = 42; AABBDD) . Only 12 of the 14 possible ditelosomic addition lines could be developed, as the monosomic addition involving chromosome 1H was self-sterile, due to the presence of the Shw sterility gene on the long arm of this chromosome . A ditelosomic addition line involving barley chromosome 1HS was developed later . The wheat-barley chromosome and chromosome arm addition lines are used for assigning genes to chromosomes and chromosome arms and for the characterization of the expression pattern of barley genes in the wheat genetic background. Wheat-barley hybrids can be used for studying the homoeologous relationship between wheat and barley genomes at chromosome level [11, 12]. The barley resistance genes can also be effective in the genetic background of wheat , at the same time wheat-barley introgression lines could be an excellent tool for the tranfer of earliness, favourable amino acid composition, biotic stress resistance, salt and drought tolerance, or good tillering ability from barley into wheat . Wheat-barley ditelosomic addition lines, on the other hand, can act as bridging materials for generating wheat-barley translocations, which are more stable than aneuploids.
The aim of this work was to select fertile, genetically stable, wheat-barley ditelosomic addition lines from backcrossed progenies of the Asakaze/Manas wheat-barley hybrid produced earlier in Martonvásár [13, 14]. Barley chromosomes were detected in the wheat background using genomic in situ hybridization (GISH), and identified with fluorescence in situ hybridization (FISH) and molecular (SSR and STS) markers specific for barley chromosome arms. The morphological characters, yield components and salt stress response of the ten lines were also investigated.
In situ hybridization
Mitotic chromosome spreads from germinating root tips were prepared as described by Lukaszewski et al. . The ditelosomic addition lines were selected using GISH from the BC2F2-BC2F4 generations and identified by FISH using repetitive DNA probes. The GISH experiment was carried out as described by Molnár-Láng et al. . Barley total genomic DNA was labelled with digoxigenin-11-dUTP (Roche Diagnostics, Mannheim, Germany) with a nick translation mix and used as a probe. Unlabelled wheat genomic DNA was used as blocking DNA at a ratio of 35:1. Detection was carried out with anti-digoxigenin-Rhodamine (Roche). The slides were mounted in Vectashield antifade solution (Vector Laboratories, Burlingame, USA) containing 2 μg/mL 4′-6-diamidino-2-phenylindole (DAPI). After rinsing off the GISH hybridization signals in 4 × SSC Tween at room temperature, FISH was carried out using the (GAA)7 microsatellite probe , the barley subtelomere-specific probe HvT01  and barley centromere-specific sequences (AGGGAG)4 . The (GAA)7 microsatellite probe was amplified and labelled with biotin-16-dUTP using PCR. The barley subtelomeric sequence HvT01 was labelled combinatorially with 50 % biotin-16-dUTP and 50 % digoxigenin-11-dUTP. The barley centromere-specific sequences (AGGGAG)4 were labelled with digoxigenin-11-dUTP. Wheat-specific DNA repetitive probes (pSc119.2, Afa family and pTa71) were used to identify the presence of the entire wheat genome. The repetitive DNA sequences Afa family  and pSc119.2  were amplified and labelled with digoxigenin-11-dUTP and biotin-16-dUTP, respectively, using PCR. The 45S rDNA clone pTa71  was labelled with 50 % biotin-16-dUTP and 50 % digoxigenin-11-dUTP by nick translation. Digoxigenin and biotin signals were detected using anti-digoxigenin-Rhodamine Fab fragments and streptavidin-FITC (Roche), respectively. The slides were screened using a Zeiss Axioskop-2 fluorescence microscope equipped with filter sets appropriate for DAPI, FITC, Rhodamine and the simultaneous detection of FITC and Rhodamine (double filter set). Images were captured with a Spot CCD camera (Diagnostic Instruments, Sterling Heights, USA) and processed with Image Pro Plus software (Media Cybernetics, Silver Spring, USA).
SSR and STS marker analysis
Genomic DNA was extracted from fresh young leaves of wheat cultivar Asakaze, barley cultivar Manas and the ten Asakaze/Manas wheat-barley ditelosomic addition lines using Quick Gene-Mini80 (FujiFilm, Japan) with a QuickGene DNA tissue kit (FujiFilm, Japan) according to the manufacturer’s instructions. The following set of barley chromosome arm-specific SSR markers and gene-specific STS markers was selected: HvCSLF4-2HS , Bmag0125-2HL , HvLTPPB-3HS , HvM60-3HL , HvM40-4HS , HvM67-4HL , Bmac0316-6HS , EBmac0806-6HL , Bmac0031-7HS  and HvCslF6-7HL . All the primer pairs were tested on DNA templates containing: genomic DNA from wheat cultivar Asakaze, barley cultivar Manas and the Asakaze/Manas ditelosomic addition lines. The PCR amplification was performed under the conditions described by Molnár et al. . The primer sequences and annealing temperatures used in this study are presented in Additional file 1. The PCR products were separated with a Fragment Analyzer™ Automated CE System equipped with a 96-Capillary Array Cartridge (Advanced Analytical Technologies, USA). The results were analysed using PROsize v2.0 software (Advanced Analytical Technologies, USA).
Phenotypic characterization of the plants, and statistical analysis
The Asakaze/Manas wheat-barley ditelosomic addition lines 2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 6HS, 6HL, 7HS and 7HL, the parental genotypes Asakaze, Chinese Spring and Manas and the Asakaze/Manas disomic addition lines were grown in phytotron chambers (Conviron PGV96) in Martonvásár. Vernalization was carried out at 4 °C for 6 weeks, and the plants were grown until tillering under an initial 15 °C day:10 °C night temperature, 12 h light:12 h dark photoperiod, 200 μmol m−2s−1 light intensity (at pot level) and 75 % relative humidity . The temperature rose by increments of 2 °C after tillering (day length 14 h), stem elongation (16 h illumination) and flowering, and 2 weeks after fertilization. The phenotypic analysis was performed on 10 plants from each genotype. The same genotypes were sown in the field in Martonvásár with 10 seeds in each 1 m row and a row distance of 15 cm. Ten plants were randomly selected from each genotype for analysis. Plant height and tillering were determined immediately before harvest. The length of the main spike, spikelets/main spike, seeds/main spike and seeds/plant were measured after harvest.
The morphological traits of the ditelosomic addition lines were compared with those of the Asakaze and Chinese Spring wheat genotypes using Student’s t test for paired data at the P = 0.05 significance level.
Evaluation of the flowering date of Asakaze/Manas ditelosomic addition lines
The flowering time of 10 plants was recorded for each genotype in the field experiment. Statistical analysis was performed using Student’s t test for paired data on the flowering date and significant differences at the P = 0.05 significance level.
Evaluation of the salt stress response of Asakaze/Manas ditelosomic addition lines
The salt stress response of seedlings of Asakaze/Manas ditelosomic addition lines was screened and compared to that of wheat and barley. The other wheat crossing parent Chinese Spring was not used in these investigations, as it had similar or lower salt tolerance than Asakaze, as demonstrated in earlier investigations . In the germination test, 3× 20 seeds of each genotype per treatment were surface-sterilized in 10 % sodium hypochlorite for 15 min, rinsed twice in distilled water and germinated on wet filter paper containing 0, 100, 200 or 250 mM NaCl in Petri dishes for 3 days at a temperature of 25 °C. The percentage of germinated seeds and the length and weight of roots and coleoptiles were determined.
Selection, identification and morphological characterization of the wheat-barley ditelosomic addition lines
The number of seeds examined for the development of each wheat-barley ditelosomic addition line
Barley chromosomes detected in the seeds analysed
Barley chromosomes eliminated
Number of seeds examined
The 3HS chromosome addition was selected from the progenies of a 3H monosomic addition, while the 3HL was identified among the descendants of a 3H disomic addition. After detecting the barley chromatin using GISH, the 3HS and 3HL additions were identified with the help of the HvLPTTB and HvM60 SSR markers, respectively (Fig. 4). The 3HS line had laxed spikes with awnstubs, while the 3HL line had short, awnless spikes with a denser structure (Fig. 5). In both phytotron and field experiments the 3HL line had one of the shortest spikes of all the ditelosomic additions developed, yet the 1000-kernel weight calculated for the field experiment was better than that of almost all the other ditelosomic and disomic addition lines (Additional files 2 and 3).
The 4HS and 4HL ditelosomic addition lines were derived from the 4H monosomic addition line. Telocentric barley chromosomes were identified in the wheat background on the mitotic chromosome spreads of its progenies using GISH. The cytological identification was confirmed using SSR markers specific for the 4HS (HvM40) and 4HL (HvM67) barley chromosome arms (Fig. 4). The 4HS telocentric chromosome was eliminated from the analysed plants with the highest frequency (Table 1), while the homozygous 4HS ditelosomic addition was quite stable. The 4HS line had flared spikes with awnstubs, while 4HL had shorter, dense spikes also possessing awnstubs (Fig. 5). The 4HL ditelosomic addition plants were the shortest in the series of ten ditelosomic addition lines; the plant height was significantly lower than that of the wheat genotypes both in the phytotron and in the field. The fertility of both the 4HS and 4HL lines was better than that of the other eight ditelosomic addition lines, both in the phytotron and in the field experiment (Additional files 2 and 3).
A double monosomic addition line carrying the 6H and 7H barley chromosomes was the parental genotype for the 6HS, 6HL and some of the 7HL wheat-barley ditelosomic additions. The telocentrics of the 6H chromosome were transmitted with higher frequency than that of the 7H. The 7HS arm was not detected in the progenies of these plants. The arms of the 6H chromosome were detected using GISH and identified with barley arm-specific SSR markers. The Bmac0136 marker revealed the presence of the 6HS barley chromosome arm, while the EBmac0806 confirmed the presence of 6HL (Fig. 4). The 6HS line had long spikes with apical awnstubs, while the 6HL spike was awnless (Fig. 5).
The 7HS and 7HL addition lines were selected from the the progenies of the 7H monosomic addition. The cytogenetic identification of the barley chromatin in the wheat background was followed by SSR and STS marker analysis, using the Bmac0031 SSR and HvCSLF6 STS markers, which distinguished the 7HS and 7HL barley chromosome arms, respectively (Fig. 4). Though the 7HL ditelosomic adition line was stable, more than two telocentric chromosomes were detected in some of the mitotic chromosome spreads of homozygous plants. As GISH did not reveal the barley origin of these chromosomes, FISH was applied on the same chromosome preparations after washing off the GISH signals. Wheat-specific FISH probes (pSc119.2, Afa family and pTa71) were used to identify the fragmented wheat chromosome. In all the preparations analysed this was found to be the 4B chromosome. Both the 7HS and 7HL additions had awnless spikes that were not very dense, but the 7HS spike was much longer (Fig. 5). In plants carrying the fragmented 4B wheat chromosome, the spikes of the 7HL addition were much shorter and had very low fertility. The fertility of the 7HS line was also low, as its spikes had many sterile spikelets on the apical part.
Stability of the Asakaze/Manas ditelosomic addition lines, investigated in the progenies of homozygous ditelosomic plants
Number of progenies of ditelosomic analysed
Rate of ditelosomics among progenies
Evaluation of flowering time of Asakaze/Manas ditelosomic addition lines in the field experiment
Average flowering date of the genotype analysed (No. of days from 1st January 2015)
Average flowering date
Evaluation of the salt stress response of Asakaze/Manas ditelosomic addition lines
In previous experiments several wheat/barley addition and translocation lines carrying chromosomes from different wheat and barley cultivars were studied for aluminium and salt tolerance [29, 30]. A comparison of the salt stress responses of Asakaze/Manas wheat–barley disomic addition lines (2H, 3H, 3HS, 4H, 6H, 7H and 7HL) to those of the parental genotypes (Asakaze, Manas and Chinese Spring) revealed that the disomic addition line 7H and the ditelosomic line 7HL exhibited higher salt tolerance both during germination and in the early developmental stages than the wheat parents, among which Asakaze had higher salt tolerance than Chinese Spring . The present experiment using a set of ditelosomic lines (2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 6HS, 6HL, 7HS and 7HL) confirmed the previous results. The ditelosomic line 7HS showed a higher reduction in growth under salt stress conditions than the wheat parent Asakaze, and the ditelosomic line 7HL and the barley parent Manas exhibited higher salt-tolerance at germination than Asakaze. These results suggest that lines carrying the long arm of the 7H barley chromosome in the wheat background could be used as genetic material for improving the salt tolerance of wheat. Higher root and shoot growth was also observed in the ditelosomic lines 2HL and 4HS than in wheat Asakaze during germination under control and mild salt stress conditions, but this improved vigour disappeared under severe salt stress, indicating that the intense growth was not related to the salt stress response. Intense root growth was also observed previously in 4H disomic addition lines , and the present results demonstrate that this is associated with the 4HS chromosome arm.
The present paper reports the development of a new set of wheat-barley ditelosomic addition lines (2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 6HS, 6HL, 7HS and 7HL) obtained by incorporating the chromosomes of the six-rowed Ukrainian winter barley cultivar Manas into the facultative Japanese wheat cultivar Asakaze. The 5HS and 5HL ditelosomics could not be selected from the Asakaze/Manas combination, as the 5H chromosome was eliminated most frequently from the backcross progenies and the plant carrying the arms of this chromosome was sterile . Each ditelosomic addition line developed contained the full complement of wheat chromosomes and a single telocentric chromosome pair from barley, though in some of the plants analysed wheat chromosome breakages or chromosome duplications were observed. Barley telocentric chromosomes may result from the misdivision of barley univalents during meiosis. The first and as yet only near complete set of wheat-barley ditelosomics, including 13 of the 14 possible ditelosomic addition lines (except 1HL) was produced by Islam in the 80’s through the addition of barley chromosomes from the Betzes barley cultivar to the Chinese Spring wheat cultivar. These lines were characterized on the basis of their morphological, physiological and biochemical features and the N-banding analysis of the chromosomes . The newly developed Asakaze-Manas wheat-barley ditelosomic addition lines were identified using GISH, FISH and molecular marker analysis, while the morphological traits and yield components were studied in phytotron and field experiments.
Manas is a winter barley cultivar with good winter hardiness making it better adapted to Central European climatic conditions than Betzes. It also has favourable agronomic traits, including good yielding ability  and better salt and aluminium tolerance than the other two barley genotypes previously used to develop addition lines [28–30]. Wheat-alien ditelosomic additions have also been developed using other cultivated and wild relatives of wheat, including various cultivars of rye, Aegilops species, Thinopyrum ponticum, Elymus species, Leymus racemosus and Hordeum chilense. These ditelosomic addition lines can be utilized for a wide range of purposes [31–40].
The development of Chinese Spring/Betzes wheat-barley ditelosomic additon lines opened the door for the flow sorting of barley telocentric chromosomes at high purity , making it possible to construct chromosome arm-specific DNA libraries and to perform the cytogenetic mapping needed for the development of physical contig maps . Mayer et al.  reported the use of flow-sorted barley chromosome 1H and chromosome arms 2HS to7HL to construct a high resolution sequence-based gene map containing an estimated 86 % of the genes in the barley genome. It also proved possible to strech flow-sorted plant chromosomes longitudinally, thus increasing the physical resolution of maps constructed using FISH .
The most widespread wheat-alien introgression is the 1BL.1RS wheat-rye tranlocation where the 1RS chromosome arm carries resistance genes to biotic and abiotic stresses, and genes affecting yield potential or protein content. The 1BL.1RS translocation is present in several hundreds of wheat cultivars, and has therefore received great attention from researchers and breeders. Flow-sorted 1RS chromosomes from the 1RS wheat-rye (Chinese Spring-Imperial) ditelosomic addition line were used to construct BAC libraries specific for 1RS rye chromosome. Chromosome arm-specific BAC libraries make it possible the high-resolution analysis of a particular region of complex plant genomes and developing molecular markers for these regions .
With the help of the Chinese Spring-Aegilops geniculata 5Mg ditelosomic addition line, the arm of an Aegilops chromosome, was successfully flow-sorted for the first time and sequenced using Illumina technology. Next-generation sequencing offers a cheap way to develop sequence-based markers for the molecular analysis of Aegilops chromosomes .
The Asakaze/Manas wheat-barley ditelosomic addition lines were compared with the Asakaze/Manas disomic addition lines, previously selected from the same wheat-barley cross . As aneuploids, disomic and ditelosomic additions exhibit a certain degree of instability which necessitates regular cytological analysis. Based on the experiments carried out to date it can be concluded that the Asakaze/Manas ditelosomic addition lines are more stable than the disomic addition lines. The 3H disomic addition, in particular, showed an unexpectedly high level of chromosome instability in comparison with that developed from Mv9kr1 and Igri [9, 47], while both 3HS and 3HL were more stable during the propagation of the ditelosomic addition lines (Table 2). The transmission of the alien chromosomes was more reliable when single alien chromosomes were replaced by their telocentrics .
Introgression lines are useful for investigating heterologous expression of genes from alien chromosomes in the wheat genetic background . In previous experiments several wheat/barley addition and translocation lines carrying chromosomes from different wheat and barley cultivars were studied for aluminium and salt tolerance [29, 30]. A comparison of the salt stress responses of Asakaze/Manas wheat–barley disomic addition lines (2H, 3H, 3HS, 4H, 6H, 7H and 7HL) to those of the parental genotypes (Asakaze, Chinese Spring and Manas) revealed that the disomic addition line 7H and the ditelosomic line 7HL exhibited higher salt tolerance both during germination and in the early developmental stages than the wheat parents, among which Asakaze had higher salt tolerance than Chinese Spring . The present experiment, using a set of ditelosomic lines (2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 6HS, 6HL, 7HS and 7HL), confirmed the previous results. The ditelosomic line 7HS exhibited a greater reduction in growth under salt stress conditions than the wheat parent Asakaze, while ditelosomic line 7HL and the barley parent Manas had better salt-tolerance in the germination stage than Asakaze. These results suggest that lines carrying the long arm of 7H barley chromosome in the wheat background could be useful genetic material for improving the salt tolerance of wheat. Higher root and shoot growth was also observed in the ditelosomic lines 2HL and 4HS than in Asakaze during germination under control and mild salt stress conditions, but this improved vigour disappeared under severe salt stress, indicating that the intense growth was not related to the salt stress response. Intense root growth was also observed previously in 4H disomic addition lines , and the present results demonstrated that this is associated with the 4HS chromosome arm.
Disomic and ditelosomic addition lines can also be used for the development of wheat-alien translocation lines, which are more stable than additions. The progenies of a monosomic 7H addition line originating from the Asakaze × Manas hybrid were screened for the presence of barley chromatin, revealing the presence of a 4BS.7HL wheat-barley Robertsonian translocation . An increased (1,3;1,4)-β-D-glucan level was detected in the translocation line, demonstrating that the HvCSLF6 gene, present on the centromeric region of the 7HL chromosome arm and responsible for β-glucan production, was expressed in the genetic background of hexaploid wheat. Based on this knowledge, a compensating 7BS.7HL wheat-barley Robertsonian translocation has been developed, as homoeologous chromosomes of barley are better able to compensate the loss of a certain wheat chromosome. The 7BS.7HL translocation line was developed from a cross between the 7B monosomic Rannaya wheat cultivar and the 7H Asakaze/Manas disomic addition. Plants carrying 42 chromosomes (monosomic for the 7B wheat chromosome and for the 7H barley chromosome) were selected from the F1 generation using GISH. The F1 plants were self-fertilized and the presence of the short or long arm of the 7H barley chromosome was detected using 7H arm-specific molecular markers in the F2 generation. Six plants carrying a monosomic 7BS.7HL centric fusion were selected from the F3 generation and were selfed. In the F4 generation three plants with 42 chromosomes were identified as disomic 7BS.7HL translocations using GISH, FISH and molecular markers . The (1,3;1,4)-β-D-glucan content of the seeds will be determined after the propagation of these lines. If the HvCslF6 gene is expressed in this background, the 7BS.7HL Robertsonian translocation stock could be of potential importance for the manipulation of wheat (1,3;1,4)-β-D-glucan levels.
The present study reports the development of a set of wheat-barley ditelosomic addition lines and ways in which these lines could be used in breeding programmes and for basic research. Several of the agronomic characters of the Manas barley cultivar are better than those of the Betzes cultivar previously used for the development of wheat-barley ditelosomic addition lines. The analysis of the salt tolerance of lines carrying the 7HL chromosome arm is the first step in exploitation of these traits. However, if this genetic material is to be used in wheat breeding, it will be necessary to develop wheat-barley translocation lines carrying only a small fragment of the barley chromatin.
DAPI, 4′-6-diamidino-2-phenylindole; FISH, fluorescence in situ hybridization; GISH, genomic in situ hybridization; PCR, polymerase chain reaction; SSC, saline sodium citrate; SSR, simple sequence repeat; STS, sequence tagged site
This work was funded by the Hungarian National Scientific Research Fund (OTKA K 104382 and K112226). The research leading to these results has received funding from the European Community’s Seventh Framework Programme (FP7/2007-2013) under the grant agreement n° FP7-613556, Whealbi. AC gratefully acknowledges support from a Marie Curie Fellowship Grant (FP7-PEOPLE-2013-IEF-625671) under the seventh framework program of the European Union. The authors gratefully acknowledge the excellent technical assistance of J. Bucsi, B. Bucsi and F. Tóth. Thanks are due to Barbara Hooper for revising the manuscript linguistically.
Availability of supporting data
The data set supporting the results give in this paper is included in or referred to within the paper or in the additional files.
MML provided the genetic material for the development of the ditelosomics, designed the experiment and revised the manuscript. ET carried out the molecular cytogenetic analysis, selected the ditelosomics and carried out the morphological analysis of the plants. AC accomplished the molecular marker analysis. ÉD determined the salt response of the seedlings. ET wrote the paper. All authors read and approved the final manuscript.
For all correspondence please contact MML.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Farrer W. Some notes on the wheat “Bobs”; its peculiarities, economic value, and origin. Agric Gaz NSW. 1904;15:849–54.Google Scholar
- Kruse A. Hordeum × Triticum hybrids. Hereditas. 1973;73:157–61.View ArticleGoogle Scholar
- Islam AKMR, Shepherd KW. Incorporation of barley chromosomes into wheat. In: Bajaj YP, editor. Biotechnology in agriculture and forestry wheat, vol. 13. Heidelberg: Springer; 1990. p. 128–51.Google Scholar
- Islam AKMR, Shepherd KW. Isolation of a fertile wheat-barley addition line carrying the entire barley chromosome 1H. Euphytica. 2000;111:145–9.View ArticleGoogle Scholar
- Molnár-Láng M, Linc G, Szakács É. Wheat–barley hybridization: The last 40 years. Euphytica. 2014;195:315–29.View ArticleGoogle Scholar
- Islam AKMR, Shepherd KW, Sparrow DHB. Isolation and characterization of euplasmic wheat-barley chromosome addition lines. Heredity. 1981;46:161–74.View ArticleGoogle Scholar
- Islam AKMR, Shepherd KW, Sparrow DH. Production and characterization of wheat-barley addition lines. In: Proceedings of 5th International Wheat Genetic Symposium. Ramanujam S. New Delhi ed. India: Science Publishers Inc.; 1978. p. 365–71.Google Scholar
- Molnár-Láng M, Linc G, Sutka J. Production and molecular cytogenetic identification of wheat-barley hybrids and translocations. J Plant Biotechnol. 1999;1:8–12.Google Scholar
- Molnár-Láng M, Kruppa K, Cseh A, Bucsi J, Linc G. Identification and phenotypic description of new wheat – six-rowed winter barley disomic additions. Genome. 2012;55:302–11.View ArticlePubMedGoogle Scholar
- Islam AKMR. Ditelosomic additions of barley chromosomes to wheat. In: Proceedindgs of 6th international wheat Genetics Symposium. Sakamoto S. ed. Kyoto, Japan: Kyoto University Press; 1983. p. 233–8.Google Scholar
- Cho S, Garvin DF, Muehlbauer GJ. Transcriptome analysis and physical mapping of barley genes in wheat–barley chromosome addition lines. Genetics. 2006;172:1277–85.View ArticlePubMedPubMed CentralGoogle Scholar
- Bilgic H, Cho S, Garvin DF, Muehlbauer GJ. Mapping barley genes to chromosome arms by transcript profiling of wheat-barley ditelosomic chromosome addition lines. Genome. 2007;50:898–906.View ArticlePubMedGoogle Scholar
- Molnár-Láng M, Linc G, Logojan A, Sutka J. Production and meiotic pairing behaviour of new hybrids of winter wheat (Triticum aestivum) × winter barley (Hordeum vulgare). Genome. 2000;43:1045–54.View ArticlePubMedGoogle Scholar
- Molnár-Láng M, Novotny C, Linc G, Nagy ED. Changes in the meiotic pairing behaviour of a winter wheat-winter barley hybrid maintained for a long term in tissue culture, and tracing the barley chromatin in the progeny using GISH and SSR markers. Plant Breeding. 2005;124:247–52.View ArticleGoogle Scholar
- Lukaszewski AJ, Rybka K, Korzun V, Malyshev SV, Lapinski B, Whitkus R. Genetic and physical mapping of homoeologous recombination points involving wheat chromosome 2B and rye chromosome 2R. Genome. 2004;47:36–45.View ArticlePubMedGoogle Scholar
- Molnár-Láng M, Cseh A, Szakács É, Molnár I. Development of a wheat genotype combining the recessive crossability alleles kr1kr1kr2kr2 and the 1BL.1RS translocation, for the rapid enrichment of 1RS with new allelic variation. Theor Appl Genet. 2010;120:1535–45.View ArticlePubMedGoogle Scholar
- Pedersen C, Linde-Laursen I. Chromosomal locations of four minor rDNA loci and a marker microsatellite sequence in barley. Chromosome Res. 1994;2:65–71.View ArticlePubMedGoogle Scholar
- Schubert I, Shi F, Fuchs J, Endo TR. An efficient screening for terminal deletions and translocations of barley chromosomes added to common wheat. Plant J. 1998;14:489–95.View ArticleGoogle Scholar
- Hudakova S, Michalek W, Presting GG, ten Hoopen R, dos Santos K, Jasencakova Z, Schubert I. Sequence organization of barley centromeres. Nucleic Acids Res. 2001;29:5029–35.View ArticlePubMedPubMed CentralGoogle Scholar
- Nagaki K, Tsujimoto H, Isono K, Sasakuma T. Molecular characterization of a tandem repeat, Afa family, and its distribution among Triticeae. Genome. 1995;38:479–86.View ArticlePubMedGoogle Scholar
- Bedbrook JR, Jones J, O’Dell M, Thompson RD, Flavell RB. A molecular description of telomeric heterochromatin in secale species. Cell. 1980;19:545–60.Google Scholar
- Gerlach WL, Bedbrook JR. Cloning and characterization of ribosomal RNA genes from wheat and barley. Nucleic Acids Res. 1979;7:1869–85.View ArticlePubMedPubMed CentralGoogle Scholar
- Burton RA, Jobling SA, Harvey AJ, Shirley NJ, Mather DE, Bacic A, Fincher GB. The genetics and transcriptional profiles of the cellulose synthase-like HvCslF gene family in barley. Plant Physiol. 2008;146:1821–33.View ArticlePubMedPubMed CentralGoogle Scholar
- Ramsay L, Macaulay M, Degli IS, MacLean K, Cardle L, Fuller J, et al. A Simple Sequence Repeat-Based Linkage Map of Barley. Genetics. 2000;156:1997–2005.PubMedPubMed CentralGoogle Scholar
- Liu ZW, Biyashev RM, Maroof MA. Development of simple sequence repeat DNA markers and their integration into a barley linkage map. Theor Appl Genet. 1996;93:869–76.View ArticlePubMedGoogle Scholar
- Molnár I, Kubaláková M, Šimková H, Farkas A, Cseh A, Megyeri M, Vrána J, Molnár-Láng M, Doležel J. Flow cytometric chromosome sorting from diploid progenitors of bread wheat, T. urartu, Ae. speltoides and Ae. tauschii. Theor Appl Genet. 2014;127:1091–104.View ArticlePubMedGoogle Scholar
- Tischner T, Kőszegi B, Veisz O. Climatic programms used in the Martonvasar phytotron most frequently in recent years. Acta Agron Hung. 1997;45:85–104.Google Scholar
- Darkó É, Janda T, Majláth I, Szopkó D, Dulai S, Molnár I, Türkösi E, Molnár-Láng M. Salt stress response of wheat–barley addition lines carrying chromosomes from the winter barley “Manas.”. Euphytica. 2015;203:491–504.View ArticleGoogle Scholar
- Dulai S, Molnár I, Haló B, Molnár-Láng M. Photosynthesis in the 7H Asakaze komugi/Manas wheat/barley addition line during salt stress. Acta Agron Hung. 2010;58:367–76.View ArticleGoogle Scholar
- Darkó É, Barnabás B, Molnár-Láng M. Characterization of newly developed wheat/barley introgression lines in respect of aluminium tolerance. Am J Plant Sci. 2012;3:1462–9.View ArticleGoogle Scholar
- Riley R, Chapman V, Johnson R. The incorporation of alien disease resistance in wheat by genetic interference with the regulation of meiotic chromosome synapsis. Genet Res. 1968;12:199–219.View ArticleGoogle Scholar
- Driscoll C, Sears ER. Individual addition of the chromosomes of “Imperial” rye to wheat. Agron Abst. 1971;6.Google Scholar
- Dvorak J, Knott DR. Disomic and Ditelosomic Additions of Diploid Agropyron elongatum Chromosomes to Triticum Aestivum. Can J Genet Cytol. 1974;16:399–417.View ArticleGoogle Scholar
- Miller TE, Reader SM, Chapman V. The addition of Hordeum chilense chromosomes to wheat. In: Induced variability in Plant Breeding. C. Pudoc ed. Wageningen: Proc Eucarpia Symp, Wageningen, The Netherlands; 1982. p. 79–81.Google Scholar
- Friebe B, Tuleen NA, Gill BS. Standard karyotype of Triticum searsii and its relationship with other S-genome species and common wheat. Theor Appl Genet. 1995;91:248–54.View ArticlePubMedGoogle Scholar
- Friebe B, Tuleen N, Jiang J, Gill BS. Standard karyotype of Triticum longissimum and its cytogenetic relationship with T. aestivum. Genome. 1993;36:731–42.View ArticlePubMedGoogle Scholar
- Friebe B, Jiang J, Tuleen N, Gill BS. Standard karyotype of Triticum umbellulatum and the characterization of derived chromosome addition and translocation lines in common wheat. Theor Appl Genet. 1995;90:150–6.View ArticlePubMedGoogle Scholar
- Friebe BR, Tuleen NA, Gill BS. Development and identification of a complete set of Triticum aestivum - Aegilops geniculata chromosome addition lines. Genome. 1999;42:374–80.View ArticleGoogle Scholar
- Friebe B, Qi LL, Nasuda S, Zhang P, Tuleen NA, Gill BS. Development of a complete set of Triticum aestivum-Aegilops speltoides chromosome addition lines. Theor Appl Genet. 2000;101:51–8.View ArticleGoogle Scholar
- Wang SL, Qi LL, Chen PD, Liu DJ, Friebe B, Gill BS. Molecular cytogenetic identification of wheat-Elymus tsukushiense introgression lines. Euphytica. 1999;107:217–24.View ArticleGoogle Scholar
- Suchánková P, Kubaláková M, Kovářová P, Bartoš J, Číhalíková J, Molnár-Láng M, Endo TR, Doležel J. Dissection of the nuclear genome of barley by chromosome flow sorting. Theor Appl Genet. 2006;113:651–9.View ArticlePubMedGoogle Scholar
- Harper LC, Cande WZ. Mapping a new frontier; development of integrated cytogenetic maps in plants. Funct Integr Genomics. 2000;1:89–98.View ArticlePubMedGoogle Scholar
- Mayer KFX, Martis M, Hedley PE, Simková H, Liu H, Morris JA, et al. Unlocking the barley genome by chromosomal and comparative genomics. Plant Cell. 2011;23:1249–63.View ArticlePubMedPubMed CentralGoogle Scholar
- Valárik M, Bartoš J, Kovárová P, Kubaláková M, de Jong JH, Dolezel J. High-resolution FISH on super-stretched flow-sorted plant chromosomes. Plant J. 2004;37:940–50.View ArticlePubMedGoogle Scholar
- Bartoš J, Paux E, Kofler R, Havránková M, Kopecký D, Suchánková P, Šafář J, Šimková H, Town CD, Lelley T, Feuillet C, Doležel J. A first survey of the rye (Secale cereale) genome composition through BAC end sequencing of the short arm of chromosome 1R. BMC Plant Biol. 2008;8:95.View ArticlePubMedPubMed CentralGoogle Scholar
- Tiwari VK, Wang S, Sehgal S, Vrána J, Friebe B, Kubaláková M, Chhuneja P, Doležel J, Akhunov E, Kalia B, Sabir J, Gill BS. SNP Discovery for mapping alien introgressions in wheat. BMC Genomics. 2014;15:1–11.View ArticleGoogle Scholar
- Szakács E, Molnár-Láng M. Identification of new winter wheat - winter barley addition lines (6HS and 7H) using fluorescence in situ hybridization and the stability of the whole “Martonvásári 9 kr1” - “Igri” addition set. Genome. 2010;53:35–44.View ArticlePubMedGoogle Scholar
- Yasui H, Iwata N. Cytogenetics of ditelosomic alien addition lines in rice (Oryza sativa L.) each carrying an extra pair of telocentric chromosomes of O. punctata Kotschy. J Fac Agr - Kyushu Univ (Japan). 1998;43:1–9.Google Scholar
- Molnár-Láng M, Türkösi E, Farkas A, Cseh A, Kruppa K, Icsó D, Rakszegi M, Szakács É, Hoffmann B, Linc G. Evaluation of flowering time, ß-glucan content and tillering of wheat/barley introgression lines. In: Cereals for Food, Feed and Fuel, Challenge for Global Improvement: Eucarpia Cereals Section - ITMI Joint Conference, Book of Abstract. 359 p. Lohwasser U, Börner A.eds. Wernigerode, Germany; 2014:60.Google Scholar
- Cockram J, Jones H, Leigh FJ, O’Sullivan D, Powell W, Laurie DA, Greenland AJ. Control of flowering time in temperate cereals: genes, domestication, and sustainable productivity. J Exp Bot. 2007;58:1231–44.View ArticlePubMedGoogle Scholar
- Turner A, Beales J, Faure S, Dunford RP, Laurie DA. The pseudo-response regulator Ppd-H1 provides adaptation to photoperiod in barley. Science. 2005;310:1031–4.View ArticlePubMedGoogle Scholar
- Pourkheirandish M, Komatsuda T. The Importance of Barley Genetics and Domestication in a Global Perspective. Ann Bot. 2007;100(5):999–1008.View ArticlePubMedPubMed CentralGoogle Scholar
- Laurie DA, Pratchett N, Bezant JH, Snape JW. RFLP mapping of five major genes and eight quantitative trait loci controlling flowering time in a winter × spring barley (Hordeum vulgare L.) cross. Genome. 1995;38:575–85.View ArticlePubMedGoogle Scholar
- Sameri M, Pourkheirandish M, Chen G, Tonooka T, Komatsuda T. Detection of photoperiod responsive and nonresponsive flowering time QTL in barley. Breeding Science. 2011;61(2):183–8.Google Scholar
- Boyd W, Li CD, Grime C, Cakir M, Potipibool S, Kaveeta L, et al. Conventional and molecular genetic analysis of factors contributing to variation in the timing of heading among spring barley (Hordeum vulgare L.) genotypes grown over a mild winter growing season. Crop Past Sci. 2003;54:1277–1301.View ArticleGoogle Scholar
- Chang S-B, de Jong H. Production of alien chromosome additions and their utility in plant genetics. Cytogenet Genome Res. 2005;109:335–43.View ArticlePubMedGoogle Scholar
- Cseh A, Kruppa K, Molnár I, Rakszegi M, Doležel J, Molnár-Láng M. Characterization of a new 4BS.7HL wheat–barley translocation line using GISH, FISH, and SSR markers and its effect on the β-glucan content of wheat. Genome. 2011;54:795–804.View ArticlePubMedGoogle Scholar
- Cseh A, Türkösi E, King J, King I, Molnár-Láng M. Development of new winter wheat-winter barley 7BS.7HL Robertsonian translocation line. London: Plant Genomics Congress; 2015. pp. 30. Available online at http://www.globalengage.co.uk/ngs/posters15.pdf.