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Article

Genome-Wide Distribution of Novel Ta-3A1 Mini-Satellite Repeats and Its Use for Chromosome Identification in Wheat and Related Species

by
Tao Lang
1,
Guangrong Li
1,*,
Zhihui Yu
1,
Jiwei Ma
1,
Qiheng Chen
1,
Ennian Yang
2 and
Zujun Yang
1,*
1
Center for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China
2
Crop Research Institute, Sichuan Academy of Agricultural Sciences, Chengdu 610066, China
*
Authors to whom correspondence should be addressed.
Agronomy 2019, 9(2), 60; https://doi.org/10.3390/agronomy9020060
Submission received: 14 January 2019 / Revised: 28 January 2019 / Accepted: 28 January 2019 / Published: 29 January 2019
(This article belongs to the Special Issue Chromosome Manipulation for Plant Breeding Purposes)
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Abstract

:
A large proportion of the genomes of grasses is comprised of tandem repeats (TRs), which include satellite DNA. A mini-satellite DNA sequence with a length of 44 bp, named Ta-3A1, was found to be highly accumulated in wheat genome, as revealed by a comprehensive sequence analysis. The physical distribution of Ta-3A1 in chromosomes 3A, 5A, 5B, 5D, and 7A of wheat was confirmed by nondenaturing fluorescence in situ hybridization (ND-FISH) after labeling the oligonucleotide probe. The analysis of monomer variants indicated that rapid sequence amplification of Ta-3A1 occurred first on chromosomes of linkage group 5, then groups 3 and 7. Comparative ND-FISH analysis suggested that rapid changes occurred in copy number and chromosomal locations of Ta-3A1 among the different species in the tribe Triticeae, which may have been associated with chromosomal rearrangements during speciation and polyploidization. The labeling and subsequent use of Ta-3A1 by ND-FISH may assist in the precise identification and documentation of novel wheat germplasm engineered by chromosome manipulation.

1. Introduction

Repetitive DNA often constitutes the majority of grass genomes, but these repeated segments vary extensively from species to species in absolute amounts, sequences, and dispersion patterns [1]. Due to the rapid evolution and characteristic genomic distribution patterns, repetitive sequences have been useful for phylogenetic analysis and chromosomal identification, as well as for studying nuclear architecture [2,3]. According to the length of the repeated units and array size, tandem repeated DNA sequences can be classified into three groups, including microsatellites, mini-satellites, and satellite DNA. The mini-satellites (10–60 bp) were first described by Jeffreys et al. [4], and are usually defined as the repetition in tandem of a short (6- to 100-bp) motif spanning 0.5 kb to several kilobases [5,6]. Mini-satellites were first characterized in the human genome [4], where they share a common motif known as the core sequence [7], and were subsequently discovered in a variety of plant species [8,9,10,11]. A remarkable advance in the knowledge of repetitive sequences has occurred in recent years because of the introduction of next-generation sequencing technologies [12]. Bioinformatic pipelines or web servers have provided computational facilities for the identification of mini-satellites for next-generation sequence data [13,14,15]. The availability of genome sequences allows the development of site-specific mini-satellites, as has been reported for diploid and polyploid plant species [16,17,18,19].
Bread wheat, Triticum aestivum L., consists of three closely related subgenomes (A, B, D), and these genomes contain a high proportion (>85%) of repetitive DNA [20,21]. Universal repetitive sequences and genome-specific repetitive sequence families have been identified in Triticeae species [22]. The mini-satellite sequences in wheat and related species have been referred to as “variable number tandem repeats” (VNTRs). The identified mini-satellite sequences in T. aestivum, T. durum Desf., T. monococcum L., Aegilops speltoides Tausch, and Ae. tauschii Coss. have shown a high degree of polymorphism among the various genomes [23,24]. Probes and markers for mini-satellites have been successfully used for DNA fingerprinting [11]. Extensive analysis of such mini-satellite tandem repeats is potentially useful for combining genomic and cytogenetic studies of wheat chromosomes.
The recent completion of the genomic sequencing of T. aestivum cv. Chinese Spring (International Wheat Genome Sequencing Consortium, [25]), and also the A genome donor (Triticum urartu Thumanjan ex Gandilyan) [26], the D genome progenitor (Ae. tauschii) [27], and the tetraploid wheat, Triticum dicoccoides Schrank ex Schübl. (AABB genomes [28]), provide opportunities for the localization of repetitive sequences to chromosome physical regions. Lang et al. [29] first constructed a database of repeats according to unit size, array number, and physical coverage length of TRs in the wheat genome. The comparison of tandem repeats, including satellite repeats, at genome-wide levels may potentially shed new light on our understanding of genomic amplification through evolutionary processes [3,29,30].
The principal aim of the present study is to describe the physical location and sequence variations of a novel mini-satellite repeat, Ta-3A1, between wheat and its ancestors by genome-wide analysis. Fluorescence in situ hybridization by Ta-3A1 for chromosome identification and evolution of wheat and related species is also discussed.

2. Materials and Methods

2.1. Plant Materials

Common wheat cv. Chinese Spring (CS), Thinopyrum intermedium (Host) Barkworth & D.R. Dewey, and Th. ponticum (Podp.) Z.-W.Liu & R.-C.Wang were provided by Prof. Bikram S. Gill, Wheat Genetic and Genomic Resource Center, Kansas State University. Germplasm of Aegilops L. and Hordeum L. species were obtained from Prof. Eviatar Nevo at the Institute of Evolution, University of Haifa, Israel. The durum wheat—Dasypyrum villosum (L.) Borbás amphiploid was obtained from Prof. Huaren Jiang, Sichuan Agricultural University, China. Lines of tetraploid wheat, including T. carthlicum Nevski, T. abyssinicum L., T. durum, and T. dicoccoides, were provided by Dr. Cheng Liu, Crop Research Institute, Shandong Academy of Agricultural Sciences. Tetraploid Ae. tauschii (Zeng et al. 2012) [31], rye (Secale cereale L.), D. villosum L., hexaploid triticale cv. Currency, and the wheat—D. breviaristatum L. partial amphiploid [32] were maintained in our laboratory at the School of Life Science and Technology, University of Electronic Science and Technology of China. A list of accessions with their ploidy level and genome constitution are given in Table S1.

2.2. Identification of Tandem Repeats (TRs)

The wheat genome IWGSC RefSeq v1.0 assembly and genomic annotation was downloaded from (https://wheat-urgi.versailles.inra.fr/). The genome-wide analysis of the tandem repeats in wheat was conducted by the Tandem Repeat Finder (TRF) algorithm [33] using alignment parameters of 2, 7, and 7 for match, mismatch, and indels, respectively. The interpretation of TRs by number of copy, array, and cluster is illustrated in Figure S1. Tandem repeats annotated by TRF were divided into three classes according to the size of period distances (<20, 20–60, and >60). A nonredundant set of sequences was constructed using the program CD-HIT [34] at an 85% similarity level. The distribution and chromosomally enriched locations of the clusters of TRs in wheat genome were visualized with the assistance of a website, B2DSC (http://mcgb.uestc.edu.cn/b2dsc), according to the procedure of Lang et al. [29].

2.3. Fluorescence In Situ Hybridization (FISH)

Seedling roots from wheat and related species and wheat-alien derivatives were collected when they were about 2–3 cm long. Excised root tips were treated with nitrous oxide gas for 2 h under 1.0 MPa pressure. The treated root tips were fixed in 90% acetic acid for 10 min. After the roots were washed by distilled water, they were digested in 2% cellulase and 1% pectolyase (Yakult Pharmaceutical, Tokyo, Japan) for 55 min at 37 °C. The digested root sections were washed and then mashed to form a cellular suspension in 100% acetic acid. The cell suspensions were dropped onto glass slides for chromosome preparation according to Kato et al. [35]. The synthesized oligonucleotide probes Oligo-pSc119.2 with 5’ labeled by 6-carboxyfluorescein (6-FAM) and Oligo-pTa535 with 5’ labeled by 6-carboxytetramethylrhodamine (Tamra) were used for identifying the wheat chromosomes according to the description of Tang et al. [36]. The oligonucleotide probes were synthesized by Shanghai Invitrogen Biotechnology Co. Ltd. (Shanghai, China). The protocol of nondenaturing FISH (ND-FISH) employing synthesized probes was described by Fu et al. [37]. After ND-FISH, the chromosome squashes for sequential FISH for Oligo-3A1 labeled by 6-FAM were washed twice, each for 5 min with 0.1% Tween 20 in 2 × SSC, to remove the hybridization signals. FISH images were captured with an Olympus BX-51 microscope equipped with a DP-70 CCD camera operated by DP manager software (Olympus). Images were processed using Photoshop 3.0 (Adobe Systems Incorporated, San Jose, CA, USA).

2.4. Sequences Variation and Phylogenetic Analysis

The DnaSP version 6.0 [38] was used to compute DNA polymorphism and their variances. Multiple sequence alignments from different chromosomal regional accumulated Oligo-3A1 sequences were done using ClustalX [39] and were subsequently used for phylogenetic analyses. Maximum likelihood (ML) trees were constructed by MEGA7.0 [40], and the trees were displayed with FigTree v1.40 software (http://tree.bio.ed.ac.uk/software/figtree/). Clustered consensus sequences combined with the phylogenetic trees were displayed with the logos [41,42].

3. Results

3.1. Ta-3A1 Was One of the Top Accumulated TRs

A database of all the raw and filtered nonredundant TRs predicted for the IWGSC RefSeq v1.0 assembly by TRF is available at http://mcgb.uestc.edu.cn/tr [29]. The nonredundant TRs were classified into three classes based on their lengths of period distance (PD), specifically <20 bp, 20–60 bp, and >60 bp. The distribution of different PD sizes on individual chromosomes indicated that the copy numbers of TRs of <20 bp were more abundant than those with 20–60 bp and >60 bp (Figure 1). Interestingly, the TRs of 20–60 bp were highly accumulated within short regions of chromosomes 3A, 5A, 7A, 5B, and 5D. In order to determine the composition of the highly accumulated mini-satellite repeats in the five chromosomes, the TRs with a pattern size ≥20 bp, copy number ≥50, and percent match ≥80 were grouped. We found that a TR array with a length of 44 bp predominated (the consensus sequence was AATAATTTTACACTAGAGTTGAACTAGCTCTA TAAGCTAGTTCA). This predominating array was named TR-3A1 and consisted of 280 nonredundant arrays covering a length of 2,630,397 bp. Across all wheat chromosomes, the estimated total predicted copy number of TR-3A1 was 59,801, which was mainly distributed on the above five chromosomes with copy numbers of 14,987, 11,083, 7828, 8444, and 28,964 on chromosomes 3A, 5A, 7A, 5B, and 5D, respectively (Table 1).
The Ta-3A1 sequence was submitted as a query into the website B2DSC using default parameters (pident = 85 and qcovhsp = 80). An example of the entire genomic distribution, detailed chromosomal locations, as well as the sequence directional analysis of Ta-3A1 according to the website B2DSC appears in Figure 2. The predicted copy number and the estimated physical positions of Ta-3A1 (Figure 2a) resembled the 20–60 bp TR localizations in Figure 1, which suggested that Ta-3A1 was actually the principal predicted mini-satellite in wheat genome compared to the results of TR enrichment studies by Lang et al. [29]. The physical organization of Ta-3A1 on chromosome 5DS regions at 146–147 Mb (Figure 2b) and the head-to-head repeats of the 72.19 Mb region in chromosome 7A (Figure 2c) were indicated in detail.
Similarly, by using the B2DSC website, the copy numbers and physical locations of Ta-3A1 were also predicted for the sequenced genomes of wheat’s ancestral species, including the A genome of T. urartu [26], the D genome [27], and AABB genomes [28] (Table 1). Based on the comparison of overall genomic copy numbers of Ta-3A1 among those of the A, B, and D genomes, we found that the copy numbers on each of the corresponding chromosomes differed significantly, and the copy numbers increased from diploid to tetraploid to hexaploid wheat. The most abundant sites of Ta-3A1 were located on 5D of wheat, which was significantly higher than those on 5D of Ae. tauschii. It is likely that the copy numbers of Ta-3A1 largely increased during the polyploidization of wheat.

3.2. Sequence Variability of Ta-3A1 on Different Chromosomal Regions

The monomer sequences within each of the Ta-3A1 arrays spanning over 200 copies were aligned according to their diagnostic physical positions. A total of 17 clustered physical regions among the 3A, 5A, 7A, 5B, and 5D chromosomes, which represented from 17% to 43% of the nonredundant sequences, were analyzed for sequence variation rates (Table 2). Interestingly, despite their different degrees of abundance, mean π values of Ta-3A1 monomers for each of the chromosome regions were roughly similar (from 9.3% in 5B to 19.4% in 3A). The higher nucleotide diversity values (π) on different chromosomes and different regions may suggest that the sequence variation and rearrangements of Ta-3A1 were due to recombination events, which may be an important force generating new monomers in chromosomes 3A, 5D, and 7A.
In order to reveal the evolutionary aspects of the overall Ta-3A1 monomer sequence variation, a phylogenetic tree of the representative Ta-3A1 satDNA in all the chromosome regions was constructed. A total of 216 representative Ta-3A1 monomer sequences predicted from the wheat genome were used for constructing the phylogenetic tree (Figure S2 and Figure 3). The results suggested that the monomers from chromosome 5D were separated first, the sequences of 5A, 5B, and 3A were categorized as the second subgroup, and the 7A sequences appeared in the third group. The sequences of chromosome 3A were mainly clustered in groups 6, 8, and 9. Combining the phylogenetic tree with the physical locations of the Ta-3A1 sequences (Figure 3), we found that the Ta-3A1 sequences from 5D distributed in most groups: However, the sequences in 5B were mainly concentrated on groups 3 and 4. This suggests that the Ta-3A1 on 5D evolved several times during sequence expansion and became more active than that of the 5B chromosome.

3.3. FISH of Oligo-3A1 in Wheat

Based on the sequences of the Ta-3A1, we produced a labeled oligo probe (Oligo-3A1) for revealing the chromosome organization of Ta-3A1 by ND-FISH analysis. Mitotic metaphase chromosomes from bread wheat, durum wheat, and some related species were prepared to study the hybridization patterns of Oligo-3A1. Sequential ND-FISH with Oligo-pTa535 and Oligo-pSc119.2 was performed for the identification of individual chromosomes of wheat [36]. As shown in Figure 4, the ND-FISH hybridization patterns of Oligo-3A1 in Chinese Spring wheat displayed strong signals on pericentromeric regions on 5DS, intercalaric regions of 5AL, 3AL, and 5BL, and subtelomeric regions of both arms on 7A. The chromosomal distribution of the FISH signals were consistent with the predicted copy numbers of each chromosome (Table 1).

3.4. FISH of Oligo-3A1 in Representative Triticeae Species

In order to shed light on the genetic divergence of Ta-3A1 on representing wheat ancestral species, the chromosome preparations from T. monococcum (A genome), Ae. longissima, Ae. searsii, Ae. speltoides (S genomes), and Ae. tauschii (D genome) accessions were carried out by ND-FISH analysis (Figure 5). The results showed that the signal strengths varied from faint to strong on 5Am and 3Am to 7Am in T. monococcum (Figure 5a,d). Strong hybridization signals appeared on long arms of 5S in Ae. speltoides (Figure 5b,e), but conversely on the short arms of 5Sl in Ae. longissima (Figure 5c,f) and 5Ss in Ae. searsii (Figure 5h,k). Relatively strong signals of Oligo-3A1 were observed on 5DS of Ae. tauschii (Figure 5j,m). Therefore, the strength of signals and the localization of chromosomes varied among the wheat A, B, and D ancestral genomes.
A total of each of 12 T. durum, six T. dicoccoides, three T. carthlicum, and two T. abyssinicum accessions were studied by ND-FISH using Oligo-3A1 (Figure 5m–r, Table 3). We observed that the signals on chromosomes 3A and 7A were stable, but the strength of signals on chromosomes 5A and 5B varied extensively. Nine accessions showed strong signals on 5BL and weak signals on 5AL, and the converse was noted in two accessions. The remaining accessions had equally strong hybridization signals on 5AL and 5BL. It is interesting to note that additional discrete signals were observed on chromosome 2BL of five T. durum lines, which were derived from International Maize and Wheat Improvement Center (CIMMYT) (Figure 5m,p). The highly polymorphic FISH patterns of Oligo-3A1 were observed among tetraploid wheat accessions.
Additionally, ND-FISH with Oligo-3A1 was also conducted on chromosome preparations of other related wild diploid or polyploid species and wheat-alien species amphiploids. The identification of individual chromosomes from Secale [37], Dasypyrum [43], and Thinopyrum [44] was achieved by Oligo-pSc119.2 and Oligo-pTa535. Barley chromosomes were completely devoid of any hybridization signals of Oligo-3A1, as were D. breviaristatum chromosomes in the wheat—D. breviaristatum amphiploid. The hybridization signals of Oligo-3A1 on rye chromosome 5R (Figure 5) and in triticale (Figure 6a,b) were relatively strong, while the signals on D. villosum 5V were weak in the durum wheat—D. villosum amphiploid (Figure 6e,f). Moreover, only two chromosomes of Th. ponticum (2n = 10x = 70) appeared to carry Oligo-3A1 signals on their long arms (Figure 6c,d), and only two pairs of chromosomes with Oligo-3A1 sites (one in short arms and the other in long arms) were observed for Th. intermedium (2n = 6x = 42) (Figure 6g,h). The distribution of Ta-3A1 was polymorphic for presence/absence in different genomes or species, which suggests that the major loci were probably lost during the evolution of this polyploidy species.

4. Discussion

With the recent development of next-generation sequencing technologies, an ever-increasing number of plant species have been studied and vast amounts of sequence data accumulated. Next-generation sequencing provides a convenient way to search for the presence of mini-satellite repeated sequences [14,15]. As a major class of repetitive DNA, mini-satellites consist of tandemly organized monomers. Zakrzewski et al. [16] isolated 517 novel repetitive sequences and used them for the identification of mini-satellite families in Beta vulgaris, and they revealed that mini-satellites are moderately to highly amplified by bioinformatic analysis and southern hybridization. Mogil et al. [15] identified five distinct, interleaved mini-satellite families in the pericentromeric regions of soybean (Glycine max) chromosomes, which were mediated by >3200 intact copies. The availability of a whole-genome assembly of wheat cv. Chinese Spring also provides opportunities to examine the distribution of retrotransposons [45] and of TRs [29] at a whole-genomic level. Our recent study predicted that TRs occupy about 3–5% of wheat chromosomes [29]. Overall, the total array number of TR mini-satellites (20–60 bp) was 1,453,457, and the total length of such mini-satellites reached 129,873,148 bp in the wheat genome by TRF [29]. Martienssen and Baulcombe [46] first identified mini-satellite arrays lying upstream of an alpha-amylase gene in hexaploid wheat. Somers et al. [24] amplified mini-satellite core sequences from wheat. However, these mini-satellite arrays in wheat represented moderately repeated families of less than 100 copies per array. Tang et al. [47] reported five probes with mini-satellite sequences among ND-FISH probes as predicted by TRF, and we predicted 120 to 260 copy numbers across specific chromosome regions with total lengths of under 20 kb by B2DSC web server. The present study found that Ta-3A1 represented the highest copy number of a mini-satellite yet reported, and it covered a total length of over 2 Mb and was mainly located on five chromosomes of wheat (Figure 1). Two copies of Ta-3A1-like sequences were found in the intron 2 of Bradi1g11210.1 and the intron 4 of Bradi3g03878.1 in the Brachypodium genome. Ta-3A1 was absent from the sequenced barley genome [48]. With regard to the accumulation of Ta-3A1 in pericentromeric regions of chromosome 5D, the observed high number may have been related to centromeric specific retrotransposons (Figure 7). Just how the extensive duplication of the Ta-3A1 sequence on 5D occurred, which resulted in such great copy numbers, is as yet unexplained and needs to be further investigated. A problem exists with the identification of the short tandem repeats, which are often reshuffled and diversified and are somehow able to escape computational detection. The quality of assembly of the wheat genome needs to be improved through the use of single-molecule sequencing, optical mapping, and chromosome conformation capture technologies [49,50]. The updated assembly of wheat genome will offer unprecedented insights into the detection of the structural features and relevant evolutionary characteristics of TRs, including mini-satellites.
The sequence dynamics of a specific satDNA family may differ across genomic regions [51], populations [52], species, or higher taxonomic groups [53,54,55,56]. Consequently, detailed characterization of satDNA families has revealed that evolutionary patterns are more complex than previously anticipated. The study of mini-satellite sequence elements is essential to our understanding of the nature and consequences of genome size variation between different species and for studying the large-scale organization and evolution of grass genomes [5]. With regard to the ancestral species of Hordeum separated by a time period ranging from 11.6 to 15.6 Mya [48], the Ta-3A1 sequence might not have been amplified at all since no signals were detectable in wild and cultivated barley species. The D. breviaristatum species was also devoid of Ta-3A1 hybridization sites. It is likely that D. breviaristatum may be one of the ancestral Triticeae species after barley separation, which is consistent with data from our previous studies on seed gliadin evolution [57]. Bread wheat can strongly adapt to different climates, and one of the key factors of this characteristic is the allohexaploid genome structure, which originates from two distinct polyploidization events [58]. In the present study, we found that the copy number of Ta-3A1 was largely amplified from T. urartu (AA), Ae. tauschii (DD), and allotetraploid T. turgidum (AABB) to common wheat (AABBDD). Moreover, Ae. speltoides is cytogenetically distinct from the S genomes of other diploid and polyploid Aegilops species based on C-banding and FISH [59,60]. We also showed that the FISH patterns of Ta-3A1 appeared on the long arm of 5S in Ae. speltoides and showed close resemblance to those of the B genome in wheat. Therefore, the study of the accumulation of mini-satellite sequences can shed light on wheat genome organization and, specifically, on the role of repetitive elements by using Ta-3A1 as an example.
The satDNA family is characterized by complex features, including large variations in copy number and long-range organization of repeat units, genome location and distribution, as well as interchromosomal and intrachromosomal recombination rates [53,61,62,63,64,65]. Fluorescence in situ hybridization (FISH) using the probes of repetitive DNA sequences was used to determine their physical locations on individual chromosomes of common wheat and its relatives [66,67]. In this current study, we also found that Secale, Dasypyrum, and Thinopyrum species displayed varied FISH patterns of Ta-3A1 hybridization (Figure 6). It is possible to deduce trends in the complexity of Ta-3A1 organization during the evolution of the Triticeae tribe from wild species to cultivated species. The variability of Ta-3A1 representing mini-satellites has been used in numerous studies to identify plant chromosomes. The Ta-3A1 probe has been used to precisely identify the chromosomal breakage points in wheat—Th. intermedium introgression lines [68,69]. FISH specific hybridization sites by Ta-3A1 on Secale, Dasypyrum, and Aegilops chromosomes can also trace specific chromatin in wheat-alien introgression lines. The combination of both molecular cytogenetics and genomic research on TRs, including mini-satellites, will significantly benefit future wheat breeding activities, which focus on chromosome manipulation and engineering [29].

5. Conclusions

The mini-satellite sequences are abundantly distributed in the wheat genome, which served as powerful cytogenetic and genomic markers for germplasm enhancement and breeding practices. The present study identified a novel mini-satellite repeat Ta-3A1, and revealed its copy number and physical locations of Ta-3A1 among chromosomes of wheat and their ancestral genomes. The large sequence variation of Ta-3A1 displayed rapid evolution of mini-satellites occurred during speciation and polyploidization The Ta-3A1 based ND-FISH may be helpful for chromosome identification of wheat and related species, which can be directly used to wheat improvement by chromosome engineering.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4395/9/2/60/s1, Table S1: List of materials and their origins; Figure S1: The interpretation of TRs by numbers of individual copy, array, and cluster; Figure S2: Phylogenetic tree and sequence comparison of the Ta-3A1 repeats.

Author Contributions

Z.Y. (Zujun Yang) and G.L. designed the experiments. T.L., G.L., Z.Y. (Zhihui Yu), J.M. and Q.C. performed the experiments. Z.Y. (Zujun Yang), E.Y., and T.L. analyzed the data. Z.Y. (Zujun Yang) and G.L. wrote the paper.

Funding

This research was funded by the National Key Research and Development Program of China (2016YFD0102000), the Applied and Basic Project (2016JY0075) from the Science and Technology Department of Sichuan, China, and the National Natural Science Foundation of China (No. 31171542).

Acknowledgments

We are thankful to Ian Dundas at the University of Adelaide, Australia, for the helpful comments on the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. The copy number and distribution of tandem repeats in wheat chromosomes 3A (a), 5A (b), 5B (c), 7A (d), and 5D (e). The copy number was predicted for wheat Chinese Spring genomic sequences v 1.0 at a web server at http://mcgb.uestc.edu.cn/BD2SC with default parameters.
Figure 1. The copy number and distribution of tandem repeats in wheat chromosomes 3A (a), 5A (b), 5B (c), 7A (d), and 5D (e). The copy number was predicted for wheat Chinese Spring genomic sequences v 1.0 at a web server at http://mcgb.uestc.edu.cn/BD2SC with default parameters.
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Figure 2. The predicted physical location of Ta-3A1 in wheat genome. The overview of Ta-3A1 on five chromosomes (a), copy number in a region of 5D (b), and an array of sequences on 7A (c) were indicated, respectively. The arrows represent the mini-satellite array, and green and red arrows show the minute and plus strand, respectively.
Figure 2. The predicted physical location of Ta-3A1 in wheat genome. The overview of Ta-3A1 on five chromosomes (a), copy number in a region of 5D (b), and an array of sequences on 7A (c) were indicated, respectively. The arrows represent the mini-satellite array, and green and red arrows show the minute and plus strand, respectively.
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Figure 3. Phylogenetic tree of Ta-3A1 repeats and their physical location on five wheat chromosomes.
Figure 3. Phylogenetic tree of Ta-3A1 repeats and their physical location on five wheat chromosomes.
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Figure 4. Nondenaturing fluorescence in situ hybridization (ND-FISH) patterns of Ta-3A1 repeats in wheat Chinese Spring: The probes Oligo-pSc119.2 (green) and pTa535 (red) (a), and sequential Oligo-3A1 (green) (b), were used for ND-FISH. The copy numbers predicted by web server page B2DSC and the copy number of Ta-3A1 at the specific region of each 1-Mb scale were illustrated in karyotypes of chromosomes (c). Bar indicated 10 μm.
Figure 4. Nondenaturing fluorescence in situ hybridization (ND-FISH) patterns of Ta-3A1 repeats in wheat Chinese Spring: The probes Oligo-pSc119.2 (green) and pTa535 (red) (a), and sequential Oligo-3A1 (green) (b), were used for ND-FISH. The copy numbers predicted by web server page B2DSC and the copy number of Ta-3A1 at the specific region of each 1-Mb scale were illustrated in karyotypes of chromosomes (c). Bar indicated 10 μm.
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Figure 5. Hybridization of the ND-FISH probes on chromosomes of T. monococcum (a,d), Ae. speltoides (b,e), Ae. longissima (c,f), Ae. searsii (g,j), Secale cereale (h, k), tetraploid Ae. tauschii (i,l), T. durum (m,p), T. carthlicum (n,q), and T. dicoccoides (o,r). The probes Oligo-pSc119.2 (green) and pTa535 (red) (a–c,g–i,o–p), and sequential Oligo-3A1 (green) (d–f,j–l,p–r) were used, respectively.
Figure 5. Hybridization of the ND-FISH probes on chromosomes of T. monococcum (a,d), Ae. speltoides (b,e), Ae. longissima (c,f), Ae. searsii (g,j), Secale cereale (h, k), tetraploid Ae. tauschii (i,l), T. durum (m,p), T. carthlicum (n,q), and T. dicoccoides (o,r). The probes Oligo-pSc119.2 (green) and pTa535 (red) (a–c,g–i,o–p), and sequential Oligo-3A1 (green) (d–f,j–l,p–r) were used, respectively.
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Figure 6. ND-FISH on chromosomes of hexaploid triticale (a,b), Thinopyrum ponticum (c,d), T. durum–Dasypyrum villosum amphiploid (e,f), and Th. intermedium (g,h). The probes Oligo-pSc119.2 and pTa535 (a,c,e,g) and sequential Oligo-3A1 (b,d,f,h) were used, respectively.
Figure 6. ND-FISH on chromosomes of hexaploid triticale (a,b), Thinopyrum ponticum (c,d), T. durum–Dasypyrum villosum amphiploid (e,f), and Th. intermedium (g,h). The probes Oligo-pSc119.2 and pTa535 (a,c,e,g) and sequential Oligo-3A1 (b,d,f,h) were used, respectively.
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Figure 7. The genome collinearity of pericentromeric regions of chromosome 5D between Ae. tauschii and wheat Chinese Spring (CS).
Figure 7. The genome collinearity of pericentromeric regions of chromosome 5D between Ae. tauschii and wheat Chinese Spring (CS).
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Table
Table 1. The predicted copy numbers of Ta-3A1 on sequenced Triticum urartu, Aegilops tauschii, T. dicoccoides, and T. aestivum genomes.
Table 1. The predicted copy numbers of Ta-3A1 on sequenced Triticum urartu, Aegilops tauschii, T. dicoccoides, and T. aestivum genomes.
SpeciesChromosomeCopy NumberSpeciesChromosomeCopy Number
3A14,987T. urartu3A2304
5A11,083 5A1199
T. aestivum7A7828 7A835
5B8444T. dicoccoides3A2765
5D28,964 5A16,482
7A6449
Ae. tauschii5D5404 5B2200
Table
Table 2. Nucleotide polymorphism of the repeat features of Ta-3A1 in wheat genome.
Table 2. Nucleotide polymorphism of the repeat features of Ta-3A1 in wheat genome.
ChromosomePhysical Location (bp)NSπHd ± SDTajima’s D
3A484,160,160–484,477,359674160.1310.925 ± 0.007−1.865 *
486,643,172–486,682,396370240.1470.987 ± 0.002−1.851 *
525,926,313–525,999,776356220.1270.965 ± 0.005−2.014 *
526,002,472–526,436,8421065170.1500.959 ± 0.004−1.648
536,013,749–536,065,681280220.1440.981 ± 0.003−1.991 *
577,811,191–577,988,203685240.1550.991 ± 0.001−1.719
578,013,600–578,743,842282150.1940.713 ± 0.006−0.916
5A420,664,083–420,976,973403140.1590.520 ± 0.010−0.998
5B412,801,830–414,820,389280690.1300.765 ± 0.007−1.456
441,918,962–442,205,867616220.1270.973 ± 0.004−1.920 *
5D109,229,486–109,417,074908190.1290.948 ± 0.005−1.843 *
139,568,074–144,410,834352930.0930.263 ± 0.010−1.276
146,286,068–146,411,073762210.1490.980 ± 0.003−1.765
146,494,968–147,180,961292490.1190.693 ± 0.010−1.519
147,436,033–147,525,419570220.1430.983 ± 0.003−1.883 *
7A72,124,011–72,576,5731466140.1200.866 ± 0.008−1.743
695,384,113–695,559,280621220.1280.970 ± 0.004−1.942 *
Number of monomeric repeats sequenced (N), number of variable sites (S), nucleotide diversities (π), and haplotype diversity (Hd). Standard deviation (SD), The estimates of the number of segregating sites and the average number of nucleotide differences correlated under the neutral model (Tajima’s D). * showed significant difference at p < 0.05.
Table
Table 3. The differential hybridization patterns of Ta-3A1 among tetraploid wheat.
Table 3. The differential hybridization patterns of Ta-3A1 among tetraploid wheat.
SpeciesOriginAccessions5B5A2BL
T. dicoccoidesJapanH137++++
T. dicoccoidesIsraelH141+++++
T. dicoccoidesSyriaH177+++++
T. dicoccoidesSyriaH179 +++
T. dicoccoidesChinaH171+++
T. dicoccoidesIsraelH283++++
T. carthlicumTurkeyH149++
T. carthlicumTurkeyH94++
T. carthlicumUSAAS311++++
T. abyssinicumEthiopiaH129++
T. abyssinicumEthiopiaH131++
T. durumCIMMYTH281 H322 H268 H242+++++
T. durumCIMMYTH246++++++
T. durumCIMMYTH261+++++++
T. durumCIMMYTH242++++
T. durumCIMMYTH259++++++++
T. durumIsraelH319 H305 H299 ++++
T. durumIsraelLangdon+++
The strength of Ta-3A1 hybridization signals indicated by + (weak), ++ (medium), +++ (strong).

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Lang, T.; Li, G.; Yu, Z.; Ma, J.; Chen, Q.; Yang, E.; Yang, Z. Genome-Wide Distribution of Novel Ta-3A1 Mini-Satellite Repeats and Its Use for Chromosome Identification in Wheat and Related Species. Agronomy 2019, 9, 60. https://doi.org/10.3390/agronomy9020060

AMA Style

Lang T, Li G, Yu Z, Ma J, Chen Q, Yang E, Yang Z. Genome-Wide Distribution of Novel Ta-3A1 Mini-Satellite Repeats and Its Use for Chromosome Identification in Wheat and Related Species. Agronomy. 2019; 9(2):60. https://doi.org/10.3390/agronomy9020060

Chicago/Turabian Style

Lang, Tao, Guangrong Li, Zhihui Yu, Jiwei Ma, Qiheng Chen, Ennian Yang, and Zujun Yang. 2019. "Genome-Wide Distribution of Novel Ta-3A1 Mini-Satellite Repeats and Its Use for Chromosome Identification in Wheat and Related Species" Agronomy 9, no. 2: 60. https://doi.org/10.3390/agronomy9020060

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