- Research article
- Open Access
Evolution of ribosomal DNA-derived satellite repeat in tomato genome
- Sung-Hwan Jo†1, 3, 7,
- Dal-Hoe Koo†1, 6,
- Jihyun F Kim2, 3,
- Cheol-Goo Hur1, 7,
- Sanghyeob Lee1, 5,
- Tae-jin Yang4,
- Suk-Yoon Kwon1 and
- Doil Choi4Email author
© Jo et al; licensee BioMed Central Ltd. 2009
- Received: 25 November 2008
- Accepted: 08 April 2009
- Published: 08 April 2009
Tandemly repeated DNA, also called as satellite DNA, is a common feature of eukaryotic genomes. Satellite repeats can expand and contract dramatically, which may cause genome size variation among genetically-related species. However, the origin and expansion mechanism are not clear yet and needed to be elucidated.
FISH analysis revealed that the satellite repeat showing homology with intergenic spacer (IGS) of rDNA present in the tomato genome. By comparing the sequences representing distinct stages in the divergence of rDNA repeat with those of canonical rDNA arrays, the molecular mechanism of the evolution of satellite repeat is described. Comprehensive sequence analysis and phylogenetic analysis demonstrated that a long terminal repeat retrotransposon was interrupted into each copy of the 18S rDNA and polymerized by recombination rather than transposition via an RNA intermediate. The repeat was expanded through doubling the number of IGS into the 25S rRNA gene, and also greatly increasing the copy number of type I subrepeat in the IGS of 25-18S rDNA by segmental duplication. Homogenization to a single type of subrepeat in the satellite repeat was achieved as the result of amplifying copy number of the type I subrepeat but eliminating neighboring sequences including the type II subrepeat and rRNA coding sequence from the array. FISH analysis revealed that the satellite repeats are commonly present in closely-related Solanum species, but vary in their distribution and abundance among species.
These results represent that the dynamic satellite repeats were originated from intergenic spacer of rDNA unit in the tomato genome. This result could serve as an example towards understanding the initiation and the expansion of the satellite repeats in complex eukaryotic genome.
- Long Terminal Repeat
- Segmental Duplication
- Tomato Genome
- Satellite Repeat
- Long Terminal Repeat Retrotransposon
The large variety of genome sizes found throughout the plant kingdom is mainly attributed to species-specific differences in ploidy and repetitive DNA content . Repetitive DNA can be divided into two categories: interspersed repeats, which are individual repeat units that are distributed around the genome in an apparently random fashion, and tandem repeated DNA, whose repeat units are placed next to each other in an array. Several previous studies have uncovered interspersed repeats, the retrotransposons, which are usually the most abundant form of repetitive DNA in plants with large genomes [2, 3]. The transposition mechanism of these repeats has been well characterized with respect to interspersed repeats. Multigene families including ribosomal RNAs (rRNA) as well as noncoding sequences such as satellite DNA, minisatellite sequences and microsatellite sequences are often arranged in tandem arrays [4, 5]. Tandemly repeated DNA is primarily found at centromeres, subtelomeric regions, and heterochromatin. Recently, a number of new satellite repeats have been described in higher plants using cytological techniques [6–8].
Ribosomal DNA is one of the most well-characterized tandem arrays and is made up of genes that are transcribed into the components of the ribosome . The repeated unit consists of the 18S, 5.8S, and 25S rRNA genes, external transcribed spacers, internal transcribed spacers, and an intergenic spacer (IGS). The coding regions of rDNA are highly conserved among eukaryotic organisms, whereas the sequence of the noncoding IGS region varies broadly between even closely-related species. This observation has been explained by the model of horizontal or concerted evolution, originally proposed by Brown et al. . The identity of coding sequences from different species can be explained to have occurred through the maintenance of sequences with strong purifying selection. However, in plants, such as legumes , potato , and tobacco [7, 13], highly amplified satellite repeats with sequence homologous to the IGS subrepeats of rDNA have been reported to exist in dispersed patterns over several chromosomes. In these genomes, the IGS subrepeat-homologous satellite sequences occur in blocks independent of the rRNA gene cluster [12, 14, 15]. The satellite sequences described in plants often have erratic distributions and large differences in abundance, between even closely related species [7, 15]. The discovery of satellite repeats homologous to the IGS of 45S rDNA induced speculation that satellite repeats might be originated from 45S rDNA. The mechanism of satellite repeat generation has been explained by several hypotheses. (1) Satellite repeats could have arisen through repeated and random unequal crossing over , (2) by replication slippage and unequal crossing over with subsequent expansion , and (3) by the products of rolling circle replication of extrachromosomal circular DNAs that became re-inserted into the genome [18, 19]. The segmental duplication of large arrays of satellite repeats has also been proposed to be the primary mechanism responsible for their amplification, contributing to the rapid reshuffling of CentO satellites in rice centromere [20, 21]. However, to date, there is no clear explanation on how the sequence of the rDNA unit escaped from the highly efficient concerted evolutionary mechanisms that keep it so well conserved. To better understand the origins of satellite repeats, it is necessary to find and compare sequences from genomes in different stages along the path of satellite repeat generation . Here we report the discovery of a satellite repeat that is highly homologous to IGS of the 18S–25S rRNA genes in tomato. The comparison of sequences from several BAC clones containing rDNA in various stages of modification has provided a plausible explanation for how IGS homologous satellite repeats were developed from the well-conserved rDNA unit.
Cytological localization of 45S rDNA and IGS-homologous repeats in the tomato genome
In order to test our hypothesis, we performed FISH analysis with a tomato-specific IGS probe (pIGS) made from 483 bp of tomato sequence amplified from the type I subfamily IGS of 25-18S rDNA (Figure 1C). Like the tomato 45S rDNA probe and unlike the wheat 45S rDNA probe, the tomato type I IGS probe hybridized to loci on four chromosomes. FISH analysis on extended DNA fibers prepared from S. lycopersicum confirmed that there are two types of IGS organization in the tomato genome (Figure 1D). One is co-localized with the coding sequence of rRNA genes and the other is linearly stretched over a 300 kb region that lacks rRNA genes. Because FISH analysis had demonstrated that the HBa0007F24 clone is derived from the same chromosomes that hybridize to the tomato 45S rDNA probe, a probe was made from the partial 18S rDNA fragment of HBa0007F24 and tested in another FISH experiment (data not shown). This probe hybridized only to the NOR on the short arm of tomato chromosome 2. These data indicate that there is a single known canonical 45S rDNA block and three IGS homologous satellite repeats that are independent of rRNA genes in the S. lycopersicum genome.
Sequence analyses reveal that transition of rDNA is initiated in the NOR
To further characterize the IGS homologous repeat sequences in the tomato genome, we selected and sequenced the BAC clone, Sle0049A24 (28,040 bp), which has expanded IGS sequences at both ends, according to the results of a BLAST search of the BAC end sequence database (Figure 2C). The majority (85%, 23,858 bp) of the total 28,040 bp sequence of Sle0049A24 (GeneBank accession number: AC225927) is a long IGS stretch, which are 86% identical to subrepeat I. The remainder of the sequence (1,753 bp) is partial 25S rDNA and subrepeat II of IGS. The length of the repeated unit was well-conserved as 52–53 bp-long throughout the 21,607 bp of continuous subrepeat type I sequence.
LTR retrotransposons inserted in the 18S rDNAs were polymerized by uneven recombination
The retrotransposon encodes four proteins, retrotrans gag, reverstranscriptase, integrase core domain, chromatin organizing modifier, and has long terminal repeats (LTR) at both ends (Figure 3E). However, TRRT4 contains solo LTR, but does not encode the gag-pol gene, indicating that some of the sequence was lost through unequal recombination . The retrotransposon insertions vary in length, from 5,645 to 6,028 bp, and share 93.61% sequence identity with each other. The 18S rDNAs associated with the TRRTs have a similar degree of sequence identity to the canonical 18S rRNA gene (92–94% identity).
Because all of the retrotransposons were found at the same position, 781 bp of the 18S rDNA, with the same flanking sequences, we examined whether the TRRT transposed site-specific manner. Using the retrotransposon sequence as a query to search GeneBank (BLASTN), we identified two tomato BAC clones, C02HBa0155E05 and C06HBa0169D11, which have the same retrotransposon, but are not associated with rDNA. The flanking sequences of these retrotransposons were different from those of HBa0007F24. FISH analysis also demonstrated that the retrotransposon sequence is present on other chromosomes as various sizes of blocks supporting that the retrotransposon was not integrated in a site-specific manner (Figure 3A).
Duplication of the IGS between 25-18S rDNA sequences into the middle of 25S rRNA
The size and the number of deletion of each unit of 25S rDNA demonstrated that the deletions were accumulated (Fig 5A). For example, all units (II, III, IV, V, and VII) of 25S rDNAs in the BAC clone have a deletion of 81–82 bp at the same position 2,986–3,066 bp and the deletion frequency varies from 2 to 5. Unit IV has a single 82 bp deletion, while unit III has four such deletions. Following the number of deletions in each unit, the order of recombination can be deduced as: IV → V → III. These results indicate that 25S rDNAs harboring IGS were mainly multiplied by unequal recombination from a single variant rather than individual IGSs being recombined in parallel in their respective 25S rDNA sequences.
The duplicated IGS-like sequences in the 25S rDNA commonly contain conserved sub-family repeat sequences, namely type I subrepeat, AT rich regions, and type II subrepeat (Figure 5B). The length of IGS-like sequences inserted into 25S rDNAs varies from 1,476 bp to 2,074 bp and primarily depends on the length of the type II subrepeat, but not type I subrepeat. These data indicate that type I and type II subrepeats have been differentially regulated during molecular evolution.
Differential amplification between subfamily repeats in the rDNA intergenic spacer
To figure out the molecular mechanisms of the repeat proliferation, we performed phylogenetic analysis of 129 repeat monomers that were identified in expanded IGS in the unit IV of HBa0007F24 sequence (Figure 6C). By analyzing the most related monomers revealed by the Neighbor-Joining tree obtained (see Additional file 2), we identified 25 pairs of monomers that are arranged in four duplicated clusters of monomers. The data obtained demonstrated that segmental duplication was occurred among the amplified type I subrepeat.
Distribution of IGS-homologous repeats among closely-related tomato species
FISH analysis and the sequences of three BAC clones described in this study provide a good explanation on the origin and developmental procedures involved in the evolution of IGS-homologous satellite repeats because they contain both the original form and early stages of the variants in a genome. They also allow us to compare transitional sequences that make it possible to compare with previously proposed models.
Homogenization of the satellite repeat to single-type monomers seems to be actively conducted from the initial stage of the satellite repeat. Gene conversion and unequal crossover has been proposed as the mechanism for genome-wide homogenization of the satellite repeats [5, 16, 31]. Our results are consistent with the models in that both gene conversion and unequal crossover play a pivotal role in regional homogenization of the satellite repeats on initial step. Analysis of the duplicated IGS located in the 25S rDNA sequence indicated that the two subrepeats are differentially regulated in their copy number. While the type I subrepeat was conserved in copy number, the number of type II subrepeat sequence was decreased in different length between variants implying that repeated unequal crossover has occurred. Neighboring sequences of type I subrepeat such as 25S rDNA and the retrotransoposon may be deleted as a result of unequal crossover homogenizing the expanding repeat (Figure 2B). However, the replacement of the type II subrepeat to the type I subrepeat within the expanded IGS of 25-18S rDNA can be explained by gene conversion. Despite the amplification of copy number of type I subrepeats, the size of type I subrepeat monomers was relatively well conserved as 52–53 bp. It appears to be a common phenomenon for the size of satellite monomers to conserve nearly uniform within a genome [13, 32, 33], whereas the copy number of satellite monomers varies dramatically across species, within an organism, or on a specific chromosome between different subspecies or varieties [7, 21, 34].
In addition, we have postulated that satellite repeats sharing the same monomer can become separated from the original locus. The four signals detected with the pTa71 probe in S. lycopersicum var.cerasiforme and S. pimpinellifolium indicate that there are coding sequences of rRNA at those four loci. This situation can be explained if an rDNA block had moved to a new location outside of their original array, followed by coding region deletion and type I subrepeat amplification. However, it is more likely that the amplified IGS repeat sequence translocated outside of the rDNA array with partial coding regions attached, than that transposed sequences on multiple chromosomes independently developed satellite repeats. These assumptions are supported by our FISH results in that, with the exception of foci on the short arm of chromosome 2, very weak or no signal was detected with a partial 18S rDNA probe in S. lycopersicum var. cerasiforme and S. pimpinellifolium. Of course, rDNA coding sequence could be effectively eliminated in the satellite repeat of S. lycopersicum. In S. lycopersicum var.cerasiforme and S. pimpinellifolium, but not yet in S. lycopersicum, additional IGS-homologous satellite repeats may have been made from the original three IGS homologous satellite repeats lacking rRNA coding sequence.
Tandem repeat segments could be moved by recombinational excision of looped-out modified rDNA segments during meiotic unequal alignment of the rDNA repeating units and might re-integrate into a new location [17, 28]. Indeed, this mechanism of recombinational deletion of amplified repeats was discovered in the fourth unit of rDNA in the clone, HBa0007F24. Of course, unequal recombination or illegitimate recombination could also lead to the translocation of satellite repeats [16, 35].
Although the integration of mobile elements in rDNA loci has been reported in animal taxa, new insertions are rapidly eliminated from the rDNA locus by unequal crossover between sister-chromatids [35, 36] and that new insertions are subject to random crossovers. Strong selective pressure against inactive rDNA units eliminates these insertions from the loci [37, 38]. The LTR retrotransposon in plant genome appears to have adapted differently to survive in the rDNA locus. When the TRRT randomly inserted into the 18S rRNA gene, unequal recombination might have occurred to make the array uniform. However, instead of removing the TRRT from the rDNA, it increased the number of genes modified with the insert. Evidence of the effort to remove the TRRT is also present in the sequence: Solo LTR unaccompanied by the rest of the transposon genes may be a remnant of a retrotransposon that has been removed by unequal recombination . Similar constitution of sequence containing a rDNA variant and retrotransposons was found on the heterochromatin of Brassica rapa. . In addition, amplified satellite repeats with sequence homologous to the IGS subrepeat of rDNA have been reported in several plants [12–15], although the preferential amplification or elimination of a repeat is highly variable across species. For example, the 2D8 satellite repeat found in potatoes consists of ~3 kb monomers of AT-rich and GC-rich subrepeat clusters, showing high sequence similarity with type I and AT-rich regions of IGS in rDNA . The A1/A2 satellite repeat of tobacco has sequence similarity to regions downstream of the TIS of IGS .
We identified IGS-derived satellite repeats in tomato genome. By analyses of multiple transitional sequences, we clearly showed the origin and the growing procedure of the satellite repeat in tomato genome. Our results also suggested the molecular mechanisms of proliferation and homogenization of the satellite repeat in tomato genome by showing multiplication procedure of modified rDNA units and amplification/deletion of different subrepeats within the 45S rDNA.
Tomato plants (S. lycopersicum (LA3911), S. lycopersicum var. cerasiforme (LA4352), and S. pimpinellifolium (LA0417)) were grown in a controlled environment room at 26°C with 16 h light/8 h dark cycles.
All BAC clones used for FISH mapping were identified by screening a Heinz 608 BAC library, kindly provided by Drs. S. Tanksley and J. Giovannoni at Cornell University, Ithaca, NY, USA. BAC probes were labeled with digoxigenin-11-dUTP or biotin-16-dUTP by nick translation, according to the manufacture's protocol (Roche, Switzerland). Other DNA probes used for FISH analysis were: an rDNA probe, pTa71, containing the coding sequences for the 18S–25S rRNA genes from wheat , pIGS, TRRT, partial 18S rRNA. Probes were amplified from the clone, HBa0007F24 with the following primer pairs: partial 18S rRNA primer (F-AATGATCCTTCCGCAG GTTTACCT, R-GCTCTGTATACATTAGCATGGGATA), 25S rRNA primer (F-CGCCCTCCTACTCTTCGGGGCCTGG, R-CAGGTTAGGCGGCATTACCCGCTGA), Retrotransposon primer (F-AATGTA TACAGAGCATAGTGTGATGTCC, R-AGTGCTCAAAGAAAGCCTACTGTCACGG), and pIGS primer (F-CGACGTACCATTT GTGCTT, R-TTACCTATGGGCAGCACACATGGTC). PCR products were cloned using pGEM-T easy Vector system (Promega, Madison, WI) and sequenced.
Fluorescence in situhybridization (FISH)
The FISH procedure applied to both mitotic and meiotic chromosomes was the same as previously reported by Koo et al. . In brief, chromosomal DNA on the slides was denatured with 70% formamide at 70°C for 2.5 min, followed by dehydration in a 70%, 85%, 95%, and 100% ethanol series at -20°C for 3 min each. The probe mixture, containing 50% formamide (v/v), 10% dextran sulfate (w/v), 5 ng/μl salmon sperm DNA and 500 ng/μl of labeled probe DNA, was heated at 90°C for 10 min then kept on ice for 5 min. Twenty microliters of this mixture was applied to the denatured chromosomal DNA and covered with a glass cover-slip. Slides were then placed in a humid chamber at 37°C for 18 h. Probes were detected with avidin-FITC and anti-digoxigenin Cy3 (Roche, Switzerland). Chromosomes were counterstained with 1 μg/μl DAPI (Sigma). The signals were detected with a Cooled CCD Camera (CoolSNAP, Photometrics, Pleasanton, CA). Images were processed with software (Meta Imaging Series™ 4.6) using Leica epi-fluorescence microscope equipped with FITC-DAPI two-way or FITC-rhodamine-DAPI three-way filter sets (Leica, Japan). The final printed images were prepared with Adobe Photoshop 7.0.
Leaf nuclei were prepared, as described by Jackson et al. . A suspension of nuclei was deposited at one end of a poly-L-lysine coated slide and permitted to air dry for 10 min. STE lysis buffer (8 μl) was pipetted on top of the nuclei and the slide incubated at room temperature for 4 min. A clean cover-slip was used to slowly drag the contents along the slide. The preparation was air dried, fixed in ethanol:glacial acetic acid (3:1) for 2 min, and baked at 60°C for 30 min. The DNA fiber preparation was incubated with a probe mixture, covered with a 22 mm × 40 mm cover-slip, and sealed with rubber cement. The slide was placed in an 80°C oven in direct contact with a heated surface for 3 min, transferred to a wet chamber, which was pre-warmed in an 80°C oven for 2 min, and transferred to 37°C overnight. Post-hybridization washing stringency was the same as for FISH on chromosome spreads. Signal detection was performed according to Koo et al. .
BAC sequencing and sequence assembly
A shotgun sequencing library was constructed in the pUC118 vector for average insert sizes of 3–5 kb. BigDye Terminator chemistry v3.1 (ABI, Foster City, CA) was used for the sequencing reactions. The sequences were analyzed using an ABI3730XL automatic DNA sequencer (ABI, Foster City, CA). All of the initial sequence data obtained were analyzed with the Phred/Phrap/Consed processing . Base-calling and assembling for the individual sequences were conducted through the Phred/Phrap software. The value of the Phred scores of the sequences was 30 or higher. The completely assembled sequence was edited using Consed. Sequence editing for consensus contig formation was generated by visual confirmation, using the Sequencher 4.1.5 program (Gene codes Corp., Ann Arbor, USA)
Putative genes were primarily identified using BLASTN and BLASTX searches of GenBank http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/blast/Blast.cgi. The consensus sequence of IGS monomers previously reported by Schmidt-Puchata et al.  was used to search against the BAC sequences, HBa007F24, SLe089P21, and Sle049A24 by BLAST. Tandem repeats were identified using Tandem Repeat Finder  and edited manually in DNAMAN (Lynnon Corporation, Quebec, Canada). The monomers were extracted from IGS unit IV of HBa007F24 and then aligned using ClustalX . The alignments were edited manually if necessary. The Neighbor-Joining trees were built using the Kimura two-parameter method . MEGA 4 was employed to calculate pairwise transition and transversion mutations .
This work was supported by grants from Crop Functional Genomics Center (CG1221) of the 21st Century Frontier Research Program funded by MOEST of the Korean government. We thank to Solanaceae Genome Network (Drs. Jim Giovanoni and Steve Tanksley) at Cornell University for providing all the tomato BAC resources.
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