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Int. J. Mol. Sci. 2013, 14(8), 15330-15347; doi:10.3390/ijms140815330
Abstract: Hexaploid wheat displays limited genetic variation. As a direct A and B genome donor of hexaploid wheat, tetraploid wheat represents an important gene pool for cultivated bread wheat. Many disease resistant genes express conserved domains of the nucleotide-binding site and leucine-rich repeats (NBS-LRR). In this study, we isolated a CC-NBS-LRR gene locating on chromosome 7B from durum wheat variety Italy 363, and designated it TdRGA-7Ba. Its open reading frame was 4014 bp, encoding a 1337 amino acid protein with a complete NBS domain and 18 LRR repeats, sharing 44.7% identity with the PM3B protein. TdRGA-7Ba expression was continuously seen at low levels and was highest in leaves. TdRGA-7Ba has another allele TdRGA-7Bb with a 4 bp deletion at position +1892 in other cultivars of tetraploid wheat. In Ae. speltoides, as a B genome progenitor, both TdRGA-7Ba and TdRGA-7Bb were detected. In all six species of hexaploid wheats (AABBDD), only TdRGA-7Bb existed. Phylogenic analysis showed that all TdRGA-7Bb type genes were grouped in one sub-branch. We speculate that TdRGA-7Bb was derived from a TdRGA-7Ba mutation, and it happened in Ae. speltoides. Both types of TdRGA-7B participated in tetraploid wheat formation. However, only the TdRGA-7Bb was retained in hexaploid wheat.
NBS-LRR genes are one of the largest families of resistance genes (R gene) in plants. They encode proteins that have a central nucleotide-binding site (NBS) and a C- terminal leucine-rich repeat (LRR) . In the Arabidopsis genome there are 200 NBS-LRR class homologues . In the rice genome, there are 600 NBS-LRR class homologues . Based on the secondary structure of the N-terminus, NBS-LRR proteins are subdivided into two classes: one class carries an N-terminal Toll-interleukin 1 receptor (TIR) domain (TIR-NBS-LRR), and the other has a putative coiled-coil domain (CC-NBS-LRR). Only CC-NBS-LRR is present in monocotyledonous plants . The function of NBS-LRR genes is to participate in plant resistance to pathogens by directly/indirectly interacting with the pathogen’s effectors. The relatively conserved domain of NBS has ATP or GTP binding activity and plays a significant role in plant defense signaling . The LRR domain is a major determinant of resistance specificity, and acts as a versatile structural framework for the formation protein-protein interactions with pathogen effectors .
It appears that many NBS-LRR genes are tightly linked in clusters within plant genomes. These clusters of genes and the repeat structure in the LRRs domain provide a greater possibility for recombination and gene conversion, and contribute to a faster generation of novel resistance alleles. At the same time, some pseudogenes are produced by recombination or mutation, but they still have the NBS structure and also are expressed in the plant before accumulating enough mutation in their promoter. Most of them are expressed constitutively at a very low level with a variety of tissue specificities and are not induced by treatment with defense signals .
Disease responses caused by the NBS-LRR gene change plant metabolism and consume high energy levels . It is also believed that there are fitness costs associated with the expression of NBS-LRR genes and activation of defense response pathways in the absence of pathogens . It has often been observed that activation of a defense-related gene caused a defect in plant growth [10,11]. Some of the NBS-LRR genes might lose function due to mutations in the absence of pathogenic stress situations; non-functional genes can also promote new functional genes through intragenic recombination . Population genetic studies showed that due to the balancing selection mechanism, NBS-LRR genes and its mutant forms widely existed in natural populations of plants . The plant balances the penalty and the necessity of a resistance gene by death and reuse of NBS-LRR genes. NBS-LRR genes undergo alternative splicing . Different splicing products collaboratively play a role in the disease resistance process .
Common wheat is one of the three major cereal crops of the world and feeds about 40% of the world population . There are diploid, tetrploid and hexaploid wheats in Triticum. Allohexaplioid wheat (AABBDD, 2n = 6x =42) includes six species: T. spelta, T. macha, T. sphaerococcum, T. compactum, T. vavilovii, T. aestivum. Tetraploid wheat (AABB) includes eight species: T. dicoccoides, T. turigidum, T. carthlicum, T. dicoccum, T. durum, T. turanicum, T. polonicum, T. paleocolchicum . Common wheat arose from the spontaneous hybridization of the tetraploid wheat T. turgidum L. (AABB, 2n = 4x = 28) with the diploid goatgrass Aegilops tauschii Coss. (DD, 2n = 2x =14) . Tetraploid wheat arose from the spontaneous hybridization of the Triticum urartu (AA, 2n = 2x = 14) with the diploid Aegilops speltoides (SS, 2n = 2x = 14) . Newly formed allopolyploids are often characterized by limited genetic variation, which is called “polyploidy bottleneck” . However, R genes are expected to be variable to cope with rapidly evolving pathogens. Tetraploid wheat can be use as a gene pool for common wheat.
There are many reports about cloning plant NBS-LRR genes, functional analysis, genomic distribution, and phylogeny analysis [21–23]. However, analysis of wheat NBS-LRR genes focuses on important functional resistance gene cloning [24–26]. It still remains largely unknown about the structure and evolution of NBS-LRR genes in wheat. In this paper, we cloned an NBS-LRR gene TdRGA-7Ba from tetraploid wheat Italy 363. Analysis of the sequence of TdRGA-7B from different ploidy wheats showed that it was greatly narrowed down in polymorphism during allopolyploidization.
2.1. Amplification and Cloning of TdRGA-7Ba from Italy 363
Using a pair of primers PM3b-1880F and Pm3b-3040R, a band of approximately 750 bp was amplified by PCR assay using the cDNA of Italy 363. The fragment was inserted into PGEM-T cloning vector, and twenty clones were subsequently sequenced. A homology search was carried out for these sequences using the nucleotide BLAST search available from NCBI. One sequence was found to have >90% sequence similarity with the Pm3 like genes. In this paper, we focused only on this sequence and named it as TdRGA-7Ba.
We obtained the full-length sequence of TdRGA-7B using a combination of 5′-RACE and 3′-RACE (Figure 1a). The TdRGA-7Ba gene ORF extends 4014 bp long, and has a GC content of 46%. It encodes a protein of 1336 amino acids. As compared with the cDNA sequence, the TdRGA-7Ba gene consists of 3946 bp and 68 bp exons and a 206 bp intron from the start to the stop codon plus a 26 bp 5′ UTR and a 370 bp 3′ UTR. At 27 bp after the position of the stop codon, there is a 103 bp intron in the 3′ UTR. Blast analysis revealed that the amino acid sequence of TdRGA-7Ba had high similarity with other NBS-LRR proteins. It shared 44.7% identity over wheat powdery mildew resistance protein of PM3B (AAQ96158), and 16.0% identity to rice bacterial blight resistance protein XA1 (BAA250 68), and 15.5% homology with the Arabidoposis Pseudomonas syringae resistance protein RPM1 (NP187360). Analysis by the protein prediction websites InterProScan ( http://www.ebi.ac.uk/Tools/InterProScan) and Pfam ( http://pfam.sanger.ac.uk/search) revealed that TdRGA-7BA contained the full NBS domain Kinase 1a, Kinase 2 and Kinase 3 at the central part, and 18 LRR repeats at the C-terminal part. Analysis by the COILs software program ( http://www.ch.embnet.org/software/COILS_form.html) revealed that there was a coiled-coil domain at the N-terminus. Therefore, TdRGA-7Ba is a CC-NBS-LRR gene (Figure 1b).
2.2. Expression Analysis of the TdRGA-7Ba
To detect the expression pattern of the TdRGA-7Ba in Italy 363, primer pair R-EX-F and R-EX-R were designed to amplify gene products from Italy 363 cDNA, and the PCR products were then cloned in the TA-vector and sequenced. Sequence analysis showed that the products had only one single sequence type and was not different from the original sequence. This result suggested that the primer pair could test the expression levels of TdRGA-7Ba.
Transcription levels showed that TdRGA-7Ba was present in all tested organs: root, leaf, culm and spikelet, but was expressed at higher level in the leaf, and at lower levels in the root and spikelet (Figure 2a). One week seedlings of Italy 363 were inoculated with the powdery mildew isolate E18, and harvested for RNA isolation at 0, 6, 12, 16, 24, 48, 96 h and 7 days later. Expression tests showed there was no difference in expression between the samples (Figure 2b). This observation indicated that TdRGA-7Ba was not induced by the powdery mildew isolate E18. It resembled most NBS-LRR genes, which were not induced by treatment with defense signals .
2.3. Chromosomal Assignment of TdRGA-7B Gene
To determine the chromosomal location of the TdRGA-7B sequence we amplified the specific band from genomic DNA of the diploid wheat and Aegilops speltoides using the primer pair of R-EX-F and R-EX-R. Only the B genome source of Aegilops speltoides could amplify the band. All the nulli-tetrasomic (NT) lines of Chinese Spring could amplify the band except Nulli-7B lines. The result showed that TdRGA-7B was located on chromosome 7B (Figure 3a).
2.4. Alternative Splicing of TdRGA-7Ba
When we amplified the full length of TdRGA-7Ba by using the primers RLF and RLR from cDNA of Italy 363, we found several short bands on the agarose gel (Figure 4a). All about 10 bands were cloned and sequenced, and six different lengths of fragments represented TdRGA-7Ba gene’s different splice variants. The longest fragment was 4137-bp and the shortest was 2179-bp (from the start codon to 226-bp after the stop codon, and included the intron in the 3′UTR) (Figure 4b). All the fragments included the CC and NBS domains, but the LRR domain varied for 0 to 18 repeats.
2.5. Genetic Variation and Phylogenetic Analysis of TdRGA-7B
In order to analyze the variation of the TdRGA-7B gene, 21 accessions of tetraploid wheat from all eight species with the AABB genome (Table 1) were performed PCR in order to detect the TdRGA-7B gene sequences by using the primers R-EX-F and R-EX-R. Comparison of the genomic sequences revealed two types of variation of the TdRGA-7B gene in tetraploid wheat. In 14 accessions, TdRGA-7B gene sequences were similar to it in Italy 363, which was named the TdRGA-7Ba type. However, in the other 6 accessions it had a 21 bp and 4 bp deletion at position +1670 and +1892. The 4 bp deletion results in the TdRGA-7B an in-frame premature termination at position +1957 within the transcript, thus becoming a pseudogene, which was named the TdRGA-7Bb type. The 6 materials with TdRGA-7Bb belonged to four species: T. dicoccoides, T. turanicum, T. durum, T. turanicum (Figure 5).
In order to further study the origin and evolution of the TdRGA-7B gene and the distribution in different ploidy wheat species, we detected TdRGA-7B variation in 20 accessions of the B genome donor Ae. speltoides and 18 accessions of hexaploid wheat. In Ae. speltoides, we found TdRGA-7Ba (16 accessions) and TdRGA-7Bb (4 accessions), but in 18 accessions representing all 6 species with the AABBDD genome of hexaploid wheat, all the samples were shown to be of the TdRGA-7Bb type. A phylogenic tree was constructed using MEGA5.1 software. These sequences were constructed with a black oat sequence (FJ829744) as the out-group, which was the most similar sequence with TdRGA-7B blasted in the NCBI program. The phylogenic tree indicated that TdRGA-7Ba genotypes were more divergent, while all TdRGA-7Bb genotypes were highly similar (Figure 6). Therefore, the TdRGA-7Bb type might have emerged relatively late in the process of evolution. In other words, it came from a deletion event in the TdRGA-7Ba gene.
2.6. The Development SSR Molecular Marker for TdRGA-7B
In the NBS domain of TdRGA-7B a trinucleotide repeat of AAG was different from 8 to 16 times in our materials. It can be used as gene-derived Simple Sequence Repeat (SSR) marker to track this gene. A pair of SSR primers R7B-SSR-F and R7B-SSR-R was designed based on the end sequence of the AAG repeats by on-line software primer 3.0. It could amplify a band from 422 to 446 bp length in different wheat materials (Figure 3b).
In this paper, we have cloned an NBS-LRR gene TdRGA-7B from tetraploid wheat Italy 363. It was located on chromosome 7B. There were many R genes assigned on chromosome 7B; such as powdery mildew resistance genes Pm5 [27–30] and Pm47 , yellow rust resistance genes Yr2  and Yr6 , stem rust resistance gene Sr17 and leaf rust resistance gene Lr14 . Therefore, in chromosome 7B of wheat, there might be an enrichment area of resistance genes. TdRGA-7B may be one of the resistance genes or located near those genes. We developed an SSR marker according to the TdRGA-7B sequence. The SSR marker can be used as a co-dominant marker in tracking itself and those genes near TdRGA-7B.
In eukaryotes, alternative splicing (AS) contributes to the complexity and the diversity of gene expression . Alternative splicing has been investigated more comprehensively in human and animals. About 70%–80% of genes of humans have alternative splicing shown by microarray assay . It may change protein domain organization, protein activity and localization and might influence the interaction between protein subunits and protein post-transcriptional regulation. AS might also produce non-functional proteins . NBS-LRR genes have been reported to undergo alternative splicing . Some of the different splicing products collaboratively played a role in the disease resistance process . In our study, TdRGA-7Ba had 6 different AS, and all of them included the whole CC and NBS domains. The function of these splicing variants need further work to prove.
Hexaploid wheat was formed only about 10,000 years ago from a natural hybridization of tetraploid wheat with diploid goatgrass Aegilops tauschii. Newly formed allopolyploids are often characterized by limited genetic variation, called “polyploidy bottleneck” . However, R genes are expected to be variable in their ability to cope with rapidly evolving pathogens. Tetraploid wheat can be used as a gene pool for wheat. The main kinds of R genes are conserved in the NBS domains, which offers a way to isolate these types of sequence by PCR using degenerate primers designed based on the conserved domains. Using this approach, R Gene Analogs (RGAs) have been isolated extensively, such as in soybean , lettuce , barley , coffee , sunflower , strawberry , ginger  and cucumber . In wheat, an Mla homologue TaMla1 was cloned from Triticum monococcum and was proved to have the conserved function against powdery mildew . Many cloned RGAs are either closely linked to known R gene loci or arranged in clusters similar to R genes. However, few were focused on their evolution.
We tested the TdRGA-7B in dipoid, tetraploid and hexaploid wheat. Both the TdRGA-7Ba and TdRGA-7Bb types were detected in Ae. speltoides, which showed that the differentiation between TdRGA-7Ba and TdRGA-7Bb was before the formation of tetraploid wheat, which is 0.5 million years ago . The phylogenic tree indicated the TdRGA-7Bb to be assembled in one sub-branch, so we speculate that the formation of TdRGA-7Bb was the result of one single mutation. The fact that two types of TdRGA-7B are in the tetraploid wheat, demonstrates that both types of TdRGA-7B participated in the formation of tetraploid wheat. That is to say, at least two independent hybridization events happened at that time. However, only the TdRGA-7Bb type is in hexaploid wheat (AABBDD). This suggests that maybe only the TdRGA-7Bb participated in the formation of hexaploid wheat, or TdRGA-7Ba also participated to the process and then has been lost.
The reason of only TdRGA-7Bb existing in hexaploid wheat is speculated as follows: first, hybrid incompatibility. One of the hybrid incompatibilities is hybrid necrosis, and the resistance process to pathogen is in the content of hypersensitive necrosis. The resistance genes can induce necrosis in the hybrid as its by-product. Resistance genes recognize effectors of pathogen, so it is highly more likely to block the distant hybridization than other proteins by recognizing foreign proteins . An NBS-LRR-type disease resistance (R) gene was necessary and sufficient for induction of hybrid necrosis in intraspecific crosses of Arabidopsis thaliana . The functional TdRGA-7Ba might block the hybridization of tetraploid wheat and goatgrass and was excluded out of the hexaploid wheat. Second, fitness costs. Constitutively expressed NBS-LRR genes are not particularly useful in an environment without the existence of a counterpart pathogen, and hexaploid wheat often has gene functional redundancy because of tripled genomes. These genes tend to be lost or become pseudogenes to avoid a fitness cost to the host species . TdRGA-7Ba might have lost its value in hexaploid wheat and was thus evolutionarily excluded.
4. Experimental Section
4.1. Plant Materials T. durum
Italy 363 was kindly provided by Dr. Fangpu Han, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (Beijing, China). The wheat line Chancellor and the powdery mildew isolate E18 were kindly supplied by Dr. Xiayu Duan, Insitute of Plant Protection, Chinese Academy of Agricultural Sciences (Beijing, China). All other diploid, tetroploid and haxploid wheats (Table 1), Aegilops speltoides (the source of the B genome), diploid goatgrass Aegilops tauschii (the source of D genome) and the nulli-tetrasomic (NT) lines of Chinese Spring (CS) were collected by State Key Laboratory of Plant Cell and Chromosome Engineering (Beijing, China).
4.2. DNA, RNA Extraction and cDNA Synthesis
All wheat seedlings were grown in a growth chamber under a 16 h/8 h, 20 °C/18 °C day/night cycle with 70% relative humidity. The one-week seedlings from all plant materials were harvested, frozen immediately in liquid nitrogen, and stored at −80 °C. Genomic DNA was extracted by the CTAB method . Total RNA was extracted from leaves and other organs by TRIZOL (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s instruction. The first strand cDNA was reverse transcribed using oligo(dT)18 primers (TaKaRa, Shiga, Japan) and transcriptase (M-MLV, Promega, Madison, WI, USA) at 42 °C for 1.5 h. Control reactions included a positive RT-PCR control with tubulin specific primers (tubF-345: 5′-TGAGGACTG GTGCTTACCGC-3′ and tubR-852: 5′-GCACCATCAAACCTCAGGGA-3′, which were designed according to Triticum aestivum alpha-tubulin cDNA (TAU76558) ) and used to amplify the cDNA, and a negative control with tubulin primers, which were used to amplify the RNA to test for genomic DNA contamination.
4.3. TdRGA-7Ba Sequencing and Analysis
The Pm3b sequence  was used to design primers PM3b-1880F (5′-TCACCTAAGGTACCTTG-3′), and PM3b-3040R (5′-TTGGTGCTTCGGGTA-3′). All primers were synthesized by the Invitrogen Company (Beijing, China). PCR reactions were performed in 50 μL mixtures containing 5 μL first strand cDNA as template, 5 μL 10× PCR buffer, 4 μL dNTPs (2.5 mmol/L), 1.25 μL each primer, 0.5 μL Taq DNA polymerase and 33 μL ddH2O. Amplification cycling conditions were the following: 95 °C for 5 min, 35 cycles of 94 °C for 30 s, 57 °C for 30 s, 72 °C for 2 min, with a final extension at 72 °C for 10 min. PCR products were separated by 1% agarose gel electrophoresis. Fragments were purified using a Gel Extraction Kit (TianGen, Beijing, China) and cloned into the pGEM-T plasmid vector (Promega, Madison, WI, USA) for subsequent sequence analysis.
The full-length cDNA sequence of TdRGA-7Ba was obtained by using the SMARTer™ RACE cDNA Amplification Kit (CLONTECH, Palo Alto, CA, USA). The experiments were carried out according to the product user manual. According to the sequence of the PCR fragment, gene specific primers (GSP) were designed. 5′-RACE PCR (Rapid Amplification of cDNA Ends) was performed with the general primer UPM and 5′ GSP (5′-TCACTGAGATCCTTCTTGTTTCCAAGG-3′), and 3′-RACE with general primer UPM and 3′-GSP (5′-GTTTATGAGCAATTGTGGAAAGTTGGTAG-3′).
The RACE sequences were constructed to full length TdRGA-7Ba cDNA by DNAMAN ( http://www.lynnon.com). According to the constructed sequence, primer pair RLF (5′-TCCTCTCCACCTTGCGAG-3′) and RLR (5′-GTGTCGCCGTGCCTCTTG-3′) were designed, and used to amplify the full length cDNA and DNA sequences from Italy 363. Conserved domain prediction in TdRGA-7Ba was performed using the InterProScan ( http://www.ebi.ac.uk/Tools/InterProScan) and pfam ( http://pfam.sanger.ac.uk/search) software programs. Coiled-coil regions were predicted by COILS ( http://www.ch.embnet.org/software/COILS_form.html) software program.
4.4. The Expression Pattern of TdRGA-7Ba
The expression pattern of TdRGA-7Ba was tested by semi-quantitative PCR. The gene specific primer pair R-EX-F (5′- ATGTGGATACTCTGGCTC -3′) and R-EX-R (5′- AGCTGGAGAGCTGTTATCC -3′) were designed according to the coding region of TdRGA-7Ba. PCR products of tubulin (TAU76558) in wheat were used as the internal control. The volume of PCR reaction was 50 μL with 5 μL first-strand cDNA as the template. Reactions were performed with EX Taq Polymerase (TaKaRa), using the following profiles: 94 °C for 5 min, 27–32 cycles of 30 s at 94 °C, 30 s at 58 °C, 1.5 min at 72 °C, and with a final extension 72 °C for 10 min. The tubulin PCR assay was performed by 27 cycles and the TdRGA-7Ba PCR assay was 32 cycles. The PCR products were separated on 1.0% (w/v) agarose gels.
4.5. Chromosomal Assignment of TdRGA-7B Gene Sequence
The TdRGA-7B specific PCR band was used to test the existence of TdRGA-7B in Chinese Spring, T. urartu Thum, Aegilops speltoides (Tausch) Gren. and a series of Chinese Spring nulli-tetrasomic (CS-NT) lines. The PCR assay was performed by using the primers of R-EX-F and R-EX-R. The Products were separated on 1.0% (w/v) agarose gels.
4.6. Phylogenetic Analysis of TdRGA-7B
The TdRGA-7B fragment was amplified by the primer pair R-EX-F and R-EX-R from every material described in Table 1. Every material was performed PCR assay with tree times separately and at least three clones were sequenced from every PCR product to reduce experimental error. Phylogenetic trees were constructed from CLUSTALW alignments of the genomic DNA sequences of TdRGA-7B using the Maximum-Likelihood method available in the Mega5.1 software program ( http://www.megasoftware.net/). Confidence values for nodes were calculated using 1000 bootstraps.
4.7. The Development of the SSR Molecular Marker for TdRGA-7B
In the NBS domain of TdRGA-7B a trinucleotide repeat of AAG was different from 8 to 16 times in our materials. A pair of SSR primer R7B-SSR-F (5′-GAAAGACCACGTTAGCAC-3′) and R7B-SSR-R (5′-TTCCCAAACATCATC CAG-3′) were designed based on the end sequence of the AAG repeat by using an on-line software primer 3.0. The volume of the PCR reaction samples was 20 μL with 2 μL of DNA as template. Reactions were performed with EX Taq Polymerase (TaKaRa), using the following profiles: 94 °C for 5 min, 40 cycles of 30 s at 94 °C, 30 s at 58 °C, 30 s at 72 °C, and with a final extension of 72 °C for 10 min. The products were separated on 8% polyacrylamide gels.
In the current work, we cloned an NBS-LRR gene TdRGA-7Ba from tetraploid wheat cultivar Italy 363. Analysis of the sequence of TdRGA-7B from different ploidy wheat showed that there were two types of TdRGA-7B in dipoid and tetraploid wheat, but only the mutated TdRGA-7Bb type existed in all six species of hexaploid wheats (AABBDD). TdRGA-7Bb is a mutant of TdRGA-7Ba and was formed in Ae. speltoides. Two types of TdRGA-7B participated in the formation of tetraploid wheat, but only the TdRGA-7Bb form was retained in hexaploid wheat. This gene is greatly diminished in polymorphism during allopolyploidization.
We would like to thank Bujun Shi (Australian Centre for Plant Functional Genomics, the University of Adelaide, Australia), Daowen Wang (Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, China) for constructive suggestions on this study. We would also like to thank Hongjie Li (Institute of Crop Science, Chinese Academy of Agricultural Sciences, China) for kind assistance with the powdery mildew inoculation. This work was generously supported by the Ministry of Science and Technology of China (Grant numbers: 2011BAD07B02 and 2009CB118300).
Conflict of Interest
The authors declare no conflict of interest.
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|Species||Source designation||Genome||Genotype||GenBank accession No.|
|Ae. speltoides var ligustica||PI542240||BB||TdRGA-7Ba||KF146824|
|Ae. speltoides var ligustica||PI542241||BB||TdRGA-7Bb||KF146825|
|Ae. speltoides var. ligustica||PI542253||BB||TdRGA-7Ba||KF146827|
|Ae. speltoides var ligustica||PI554305||BB||TdRGA-7Ba||KF146834|
|Ae. speltoides var ligustica||PI560527||BB||TdRGA-7Ba||KF146835|
|T. durum||Italy 363||AABB||TdRGA-7Ba||KC990538|
|T. aestivum||Chinese Spring||AABBDD||TdRGA-7Bb||KF146875|
The RM accessions are from Chinese Crop Germplasm Resources Information Network, China;the CItr and PI accessions are from USDA-ARS, The Germplasm Resources Information Network (GRIN), USA; the TRI accessions are from Genebank Information System of the IPK Gatersleben, Germany; the KU accessions are from the National BioResource Project-wheat, Japan.
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