Molecular cytogenetic characterization of Dasypyrum breviaristatum chromosomes in wheat background revealing the genomic divergence between Dasypyrum species
© Li et al. 2016
Received: 3 December 2015
Accepted: 19 January 2016
Published: 25 January 2016
The uncultivated species Dasypyrum breviaristatum carries novel diseases resistance and agronomically important genes of potential use for wheat improvement. The development of new wheat-D. breviaristatum derivatives lines with disease resistance provides an opportunity for the identification and localization of resistance genes on specific Dasypyrum chromosomes. The comparison of wheat-D. breviaristatum derivatives to the wheat-D. villosum derivatives enables to reveal the genomic divergence between D. breviaristatum and D. villosum.
The mitotic metaphase of the wheat- D. breviaristatum partial amphiploid TDH-2 and durum wheat -D. villosum amphiploid TDV-1 were studied using multicolor fluorescent in situ hybridization (FISH). We found that the distribution of FISH signals of telomeric, subtelomeric and centromeric regions on the D. breviaristatum chromosomes was different from those of D. villosum chromosomes by the probes of Oligo-pSc119.2, Oligo-pTa535, Oligo-(GAA)7 and Oligo-pHv62-1. A wheat line D2139, selected from a cross between wheat lines MY11 and TDH-2, was characterized by FISH and PCR-based molecular markers. FISH analysis demonstrated that D2139 contained 44 chromosomes including a pair of D. breviaristatum chromosomes which had originated from the partial amphiploid TDH-2. Molecular markers confirmed that the introduced D. breviaristatum chromosomes belonged to homoeologous group 7, indicating that D2139 was a 7Vb disomic addition line. The D2139 displayed high resistance to wheat stripe rust races at adult stage plant, which may be inherited from, D. breviaristatum chromosome 7Vb.
The study present here revealed that the large divergence between D. breviaristatum and D. villosum with respected to the organization of different repetitive sequences. The identified wheat- D. breviaristatum chromosome addition line D2139 will be used to produce agronomically desirable germplasm for wheat breeding.
The genus Dasypyrum (or Haynaldia) consists of only two diploid species, the annual Dasypyrum villosum and perennial D. breviaristatum . The genomes of diploid D. villosum and D. breviaristatum were assigned the symbols V and Vb, respectively [2, 3]. Based on the sequences comparison of nr5S DNA multigene family, Baum et al.  suggested that the genome constitution of 4x D. breviaristatum should be considered as an allotetraploid VVVbVb. Dasypyrum species possess agronomically important genes such as disease resistance, high protein quality and drought tolerance, all of which represent valuable resources for global wheat breeding . The species D. villosum has been extensively hybridized with wheat for at least 6 decades, and several disease resistance genes have been successfully transferred to wheat [5–7]. Above all, over 20 elite cultivars carrying the wheat- D. villosum chromosome T6AL · 6VS translocation with powdery mildew resistance gene Pm21 have been released into agricultural production in China [8, 9]. Given the widespread success of this introgression from D. villosum, researches have been conducted with a similar aim to transfer useful genes from D. breviaristatum into wheat. Subsequently, the wheat- D. breviaristatum partial amphiploid  and wheat- D. breviaristatum introgression lines with multiply disease resistances have developed [11, 12].
Molecular and cytogenetic methods have been previously employed to assess the level of chromosomal divergence of these two Dasypyrum species [13, 14]. A large number of interspecific and intraspecific chromosome variations and significant genomic diversification were observed among different Dasypyrum accessions, probably due to the out-crossing characteristic of these two Dasypyrum species . Each pair of Dasypyrum chromosomes were transferred into a wheat background after intergeneric hybridizations. The wheat- Dasypyrum chromosome addition lines with different Dasypyrum species or accession origins allow comparison of the different Dasypyrum genomes in wheat backgrounds. In the present study, fluorescent in situ hybridization (FISH) was carried out to characterize differences between D. breviaristatum and D. villosum chromosomes by comparing karyotypes between the wheat- D. breviaristatum partial amphiploid TDH-2 and Triticum turgidum - D. villosum amphiploid TDV-1, The FISH and molecular markers were applied to identify new wheat- D. breviaristatum addition line with stripe rust resistance, which will be a useful germplasm for wheat genetics and breeding.
Comparative FISH karyotype of TDH-2 and TDV-1
FISH using probes Oligo-pSc119.2, Oligo-pTa535, Oligo-(GAA)7 were also carried out on the chromosomes of the Triticum turgidum cv. Jorc-69- D. villosum amphiploid TDV-1 (Fig. 1c and d). We found that the signals of probe Oligo-pSc119.2 were mainly located on terminal sites, while the hybridization signals of Oligo-pTa535 were distributed along the chromosome arms of D. villosum. The probe Oligo- (GAA)7 hybridized to 2V-7V of D. villosum chromosomes at their centromeric or sub-terminal regions. Moreover, we produced a high tandem repeat sequences probe Oligo-pHv62-1 as reported by Li et al. . FISH revealed that Oligo-pHv62-1 present in terminal or sub-terminal heterochromatic C-banding regions of D. villosum chromosomes in TDV-1, but was absent in D. breviaristatum chromosomes of TDH-2 (Fig. 1e and f). The comparative FISH karyotypes of the D. breviaristatum and D. villosum chromosomes allows easily to distinguish each individual Dasypyrum chromosome in wheat background.
FISH of wheat- D. breviaristatum addition line D2139
Molecular markers analysis
The primers used to localize the Vb7 specific amplification in D2139
Primer sequences (5’–3’)
Wheat bin map
Length of Vb7 bands
Agronomic traits and rust resistance analysis
With respect to the genomic relationship between two Dasypyrum species, D. breviaristatum and D. villosum, cytogenetic and molecular evidence has revealed the huge genetic divergence between the two species. Friebe et al.  established the C-banded patterns of D. villosum, and then Linde-Laursen and Frederiksen  observed extensive C-band karyotype differences between the two genomes. De Pace et al.  isolated a repeat sequence that was mapped further distally on D. villosum chromosomes using FISH compared to wheat chromosomes. Galasso et al.  found that the differentiated GISH patterns reflected the large genomic divergence between the D. villosum and D. breviaristatum chromosomes. Liu et al.  used FISH probed by a ribosomal DNA sequence and proposed a hypothesis that the diploid D. villosum and tetraploid D. breviaristatum evolved in parallel from an ancestral species. Recently, we used the pDbC2 probe to hybridize to tetraploid D. breviaristatum and diploid D. villosum chromosomes, and found more Ty3-gypsy retrotransposon copy numbers in centromeric regions of D. villosum than those in D. breviaristatum . In the present study, we compared D. breviaristatum and diploid D. villosum chromosomes through the distribution of FISH signals of Oligo-pSc119.2, Oligo-pTa535, Oligo-(GAA)7 by sequential multicolor-FISH (Fig. 1) and the molecular markers (Table 1) by PCR. The results suggested that strong evolutionary divergence involving copy number of repeated sequences and nucleotide sequence rearrangement may have occurred among Dasypyrum species during species evolution. Moreover, the Oligo-pHv62-1 can hybridize D. villosum chromosomes in TDV-1 (Fig. 1e). It confirmed that the high tandem repeat sequences present largely in telomeric heterochromatin regions of D. villosum as reported by Li et al. . However, FISH revealed that Oligo-pHv62-1 was absent in D. breviaristatum chromosomes of TDH-2 (Fig. 1f). This significant amplification of different types of repetitive sequences between the D. villosum and D. breviaristatum chromosomes may be related to adaptation of the plant species to their environments . The cytogenetic and molecular markers which are species-specific can be used to identify and characterize the introgression of D. villosum and D. breviaristatum chromosome segments into a wheat background.
Rapid genomic and epigenomic changes have been commonly found in some newly synthesized wheat-alien amphiploids [25, 26]. Alterations of alien chromosomal structure in wheat background have also been described especially wheat-rye chromosome addition, substitution and translocation lines [27, 28]. However, the variations in the karyotype of wheat chromosomes have been less reported. Recently, Fu et al.  reported that pSc119.2 FISH signals could be observed at the telomeric regions of 3DS arms which was not observed in the current material, and structural variation and abnormal mitotic behavior of the 3D chromosome were detected in the selfed progeny of wheat “MY11”-rye 6R monosomic addition line. Furthermore, Fu et al.  reported the occurrence of 14 chromosomal rearrangements in wheat -rye hybrids. Our studies found that chromosomes 1B, 2B and 7A of the wheat- D. breviaristatum partial amphiploid TDH-2 (Fig. 1), and chromosomes 1D and 3D of the 7Vb addition lines D2139 (Fig. 2) showed apparent structural changes revealed by FISH patterns compared to the parental lines. Patokar et al.  characterized several novel wheat-Thinopyrum bessarabicum recombinant lines carrying intercalary translocations and did not report any observable wheat chromosomal rearrangements using FISH. It is likely that the distant species of genera Secale and Dasypyrum may induce such structural changes while present in a wheat background, while chromosomes derived from Thinopyrum species may not have the same effect due to their close relationship to wheat . Thus, we suggest that the introgression of chromosomes from closely related species may not lead to the significant structural changes of wheat chromosomes, although the introduction of closely related Aegilops chromosomes causes massive deletions of wheat chromosomes , which were mainly useful for physical mapping of genes. There is the other possibility that the recipient wheat genotype may also increase the chromosomal rearrangement with visible changes of representative repeats. Taking advantage of fast multicolor FISH methods , we recently identified some chromosomal changes in high yielding elite cultivars originating from wheat distant hybridization. The association between the visibly rearranged wheat chromosomes and the yield or disease resistances are being verified for breeding purpose.
D. villosum chromosomes are known to contain genetic variability of value for incorporation into wheat. At least three sets of D. villosum chromosomes addition lines in wheat background have been developed [34–36]. Novel genes including disease resistance and quality-related characters have been found in different wheat- D. villosum derived lines . With the aim to transfer novel genes from D. breviaristatum to wheat, we identified the two D. breviaristatum chromosomes addition lines Y93-1-A6-4 and Y93-1-6-6, which showed novel resistance to powdery mildew isolates and stem rust Ug99 (pathotype TTKSK) . Molecular marker and GISH analysis revealed that those introduced D. breviaristatum chromosomes were rearranged chromosomes involved groups 2, 6 and 7. Recently, Li et al.  reported a wheat - D. breviaristatum substitution line D11-5 possessing a pair of 2Vb chromosomes which had replaced wheat 2D. Based on the FISH analysis, we found that the 2Vb chromosome in line D11-5 was identical to chromosome Vb2 of TDH-2 (Fig. 1). We thus suggest that chromosome Vb2 can be provisionally assigned to linkage group 2, subject to confirmation using other genetic markers.
In the present study, we identified line D2139 which contained a pair of D. breviaristatum chromosomes confirmed herein to be “7Vb”. This disomic substitution line D2139 may be potentially useful germplasm for agronomic traits including enhance spike length and the stripe rust resistance from the D. breviaristatum 7Vb into the wheat genome using marker-assisted chromosome engineering . The divergence between the individual D. villosum 7V and D. breviaristatum 7Vb chromosomes was revealed by FISH and molecular markers in wheat background, which will provide the basis for future detailed comparative genomics analysis. Guo et al.  compared chromosomes 7el1, 7el2, 7E(e), and 7Ei derived from different Thinopyrum species by molecular and cytological methods. In a similar manner, we intend to create hybrid populations between wheat- Dasypyrum 7 V and 7Vb addition lines for further and direct localization of genes on these alien chromosomes.
In summary, the different FISH patterns between D. breviaristatum and D. villosum chromosomes were observed clearly by using different repetitive sequences as probes, which allows to identify the individual Dasypyrum chromosomes in wheat background. The changes of FISH patterns of wheat chromosomes were induced by the induction of D. breviaristatum to wheat. The D. breviaristatum specific molecular markers can be used to assign the homologous group of D. breviaristatum to wheat. We identified wheat- D. breviaristatum chromosome 7Vb addition line with novel stripe rust resistances will be potential useful for wheat breeding. The molecular and cytogenetic markers will assist to trace the D. breviaristatum chromatin in wheat background.
D. breviaristatum accession PI 546317 was obtained from the National Small Grains Collection at Aberdeen, Idaho, USA. The wheat– D. breviaristatum partial amphiploid TDH-2 (genome AABBVbVb) was as described by Yang et al. . The accession of Dasypyrum villosum TA10220 and the Chinese Spring- D. villosum chromosome 7 V addition line TA7683  were obtained from Dr. Bernd Friebe of Wheat Genetic and Genomic Resources Center at Kansas State University, Manhattan, KS, USA. The T. turgidum cv. Jorc-69- D. villosum amphiploid TDV-1 (genome AABBVV) was developed and provided by Prof. Hua-Ren Jiang at Sichuan Agricultural University, China . Line D2139 was obtained from a BC1F5 generation of the crosses between wheat cultivar ‘Mianyang 11’ (MY11) and TDH-2.
Fluorescence in situ hybridization (FISH)
Seedling root tips were collected and then treated with nitrous oxide followed by enzyme digestion, using the procedure of Han et al. . The synthesized oligo-nucleotide probes Oligo-pSc119.2, Oligo-pTa535, Oligo-(GAA)7 were used for identifying the wheat chromosomes according to the description of Tang et al. . A new probe, Oligo-pHv62-1 (5’ CGAAGGATTG AAAAAAGGAA CAATTTCGCA CTTACAGCTC AAAAATATA TGGGACA 3’) was synthesized and labeled at 5’ 6-carboxyfluorescein (FAM) based on high tandem repeat sequences pHv62 in D. villosum as reported by Li et al. . The protocol of non-denaturing FISH by the synthesized probes was described by Fu et al. . Photomicrographs of FISH chromosomes were taken with an Olympus BX-51 microscope equipped with a DP-70 CCD camera.
Molecular marker analysis
DNA was extracted from young leaves of D. breviaristatum, TDH-2, TDV-1, lines D11-5 and CS . PCR-based Landmark Unique Gene (PLUG) primers were designed according to Ishikawa et al. . Polymerase chain reaction (PCR) was performed in an Icycler thermalcycler (Bio-RAD Laboratories, Emeryville, CA) in a 25 μl reaction, containing 10 mmol Tris–HCl (pH 8.3), 2.5 mmol MgCl2, 200 μmol of each dNTP, 100 ng template DNA, 0.2 U Taq polymerase (Takara, Japan) and 400 nmol of each primer. The cycling parameters were 94 °C for 3 min for denaturation; followed by 35 cycles at 94 °C for 1 min, 55 °C for 1 min, 72 °C for 2 min; and a final extension at 72 °C for 10 min. The amplified products were separated by 8 % PAGE gel as described by Hu et al. .
Disease resistance screening
Wheat- D. breviaristatum derivative lines were evaluated for adult-plant resistance to Pst strains CYR32 and CYR33 during the 2013 and 2015 cropping seasons as described by Li et al. .
We particularly thank Dr. I. Dundas at University of Adelaide, Australia, for reviewing the manuscript. We thank the National Natural Science Foundation of China (No. 31171542), and Sichuan wheat breeding community for the financial support.
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