Impact Factor 4.106 | CiteScore 4.47
More on impact ›

Original Research ARTICLE

Front. Plant Sci., 06 August 2019 | https://doi.org/10.3389/fpls.2019.00986

Alignment of Rutaceae Genomes Reveals Lower Genome Fractionation Level Than Eudicot Genomes Affected by Extra Polyploidization

Jiaqing Yuan1,2, Jinpeng Wang1,2, Jigao Yu1,2, Fanbo Meng1,2, Yuhao Zhao1,2, Jing Li1,2, Pengchuan Sun2, Sangrong Sun1,2, Zhikang Zhang1,2, Chao Liu1,2, Chendan Wei1,2, He Guo1,2, Xinyu Li1,2, Xueqian Duan1, Shaoqi Shen1, Yangqin Xie1, Yue Hou1, Jin Zhang1, Tariq Shehzad3* and Xiyin Wang1,2*
  • 1School of Life Sciences, North China University of Science and Technology, Tangshan, China
  • 2Center for Genomics and Computational Biology, North China University of Science and Technology, Tangshan, China
  • 3Plant Genome Mapping Laboratory, University of Georgia, Athens, GA, United States

Owing to their nutritional and commercial values, the genomes of several citrus plants have been sequenced, and the genome of one close relative in the Rutaceae family, atalantia (Atalantia buxifolia), has also been sequenced. Here, we show a family-level comparative analysis of Rutaceae genomes. By using grape as the outgroup and checking cross-genome gene collinearity, we systematically performed a hierarchical and event-related alignment of Rutaceae genomes, and produced a gene list defining homologous regions based on ancestral polyploidization or speciation. We characterized genome fractionation resulting from gene loss or relocation, and found that erosion of gene collinearity could largely be described by a geometric distribution. Moreover, we found that well-assembled Rutaceae genomes retained significantly more genes (65–82%) than other eudicots affected by recursive polyploidization. Additionally, we showed divergent evolutionary rates among Rutaceae plants, with sweet orange evolving faster than others, and by performing evolutionary rate correction, re-dated major evolutionary events during their evolution. We deduced that the divergence between the Rutaceae family and grape occurred about 81.15–91.74 million years ago (mya), while the split between citrus and atalantia plants occurred <10 mya. In addition, we showed that polyploidization led to a copy number expansion of key gene families contributing to the biosynthesis of vitamin C. Overall, the present effort provides an important comparative genomics resource and lays a foundation to understand the evolution and functional innovation of Rutaceae genomes.

Introduction

The genus Citrus L., belonging to the subfamily Aurantioideae in the family Rutaceae, comprises many important fruit-producing plants. Citrus is grown in at least 114 countries (Talon and Gmitter, 2008; Liu et al., 2012), and widely cultivated citrus species include sweet orange [C. sinensis (L.) Osbeck], mandarin clementine (C. clementina hort. ex Tanaka), pummelo (C. grandis Osbeck or C. maxima Merr.), grapefruit (Citrus paradisi Macf.), lemon [Citrus limon (L.) Burm. f.], and papeda (Citrus ichangensis Swingle) (Barrett and Rhodes, 1976; Moore, 2001). With a long cultivated history, citrus plays important roles for its values from daily life to commercial activity, providing rich vitamins, antioxidant compounds for healthy diets and various flavorings such as beverages (Cheong et al., 2012; Liu et al., 2012; Singh et al., 2014).

Citrus has undergone a complicated history of inbreeding and artificial breeding (Scora, 1975; Barrett and Rhodes, 1976; Nicolosi et al., 2000; Wu et al., 2014, 2018; Curk et al., 2016). Mainly for their economic importance, genome sequences of citrus plants and a close Rutaceae relative have been deciphered, including sweet orange, clementine, pummelo, papeda, citron, and atalantia (Xu et al., 2013; Wu et al., 2014; Wang et al., 2017b). The high-quality clementine genome sequence produced by the International Citrus Genome Consortium (ICGC: http://www.citrus.genome.ucr.edu/) includes 301.4 Mb with 1,398 scaffolds and L50 reached to 31.4 MB (Wu et al., 2014). The draft genome of sweet orange was released with total contig length about 320.5 Mb and 4,811 scaffolds (>500 b p) (Xu et al., 2013). The other 4 genomes were released by the same research group, including a highest-quality assembled pummelo genome with total scaffold length of about 301.95 Mb positioned to 117 scaffolds, and draft genomes of papeda, citron, and atalantia, which were not assembled to the chromosomal level yet (Wang et al., 2017b).

Polyploidization is widespread during the evolution of land plants (Soltis and Soltis, 1999; Adams and Wendel, 2005; Maere et al., 2005; Soltis et al., 2009). A core-eudicot-common hexaploidy (ECH) (Bowers et al., 2003) was revealed from the sequence of the Arabidopsis genome (The Arabidopsis Genome Initiative, 2000), and clearly deciphered with the availability of the grape genome (Jaillon et al., 2007). The ECH was also described with citrus genomes (Xu et al., 2013), tripling all chromosomes and all genes in their common ancestral genome (Soltis and Soltis, 1999; Aury et al., 2006; Soltis et al., 2009; Wang et al., 2018). After the ECH, ancestral genomes experienced extensive gene loss, genomic fractionation, and chromosomal rearrangement, most likely before the split of eudicot plants and continuing at much lower levels in each new species (Wang et al., 2005; Freeling et al., 2008; Buggs et al., 2012; Sankoff and Zheng, 2012). The extant Rutaceae genomes formed with at least 10 chromosome fusions and breakages after the ECH, in each of which thousands of ECH-duplicates or paralogous genes were preserved (Xu et al., 2013). These paralogous genes in Rutaceae plants often have their orthologs preserved, and non-orthologous paralogs from different plants are specifically called outparalogs.

The availability of citrus and related genomes provides valuable opportunities to understand their biology and evolution. However, a cross-genome characterization and comparison of genome fractionation, e.g., gene retention and loss, shared orthology among Rutaceae plants after the ECH or after their split, has not been available. Here, we aim at inferring gene collinearity within and between genomes of five citrus and one Rutaceae relative with grape as the outgroup reference, constructing intra- and inter-genomic homology due to polyploidization and speciation, and producing lists of orthologs, paralogs and outparalogs (Figure 1). Moreover, by exploring the above genome alignment, we can deduce pan-family genome fractionation. Further, we can deduce how polyploidization affected copy number variation of gene families, exemplified by vitamin C genes. Overall, the present effort provides an important comparative genomics resource for further biological exploration in Rutaceae and beyond.

FIGURE 1
www.frontiersin.org

Figure 1. Species and gene phylogenetic tree. (A) Phylogenetic tree of Vitis vinifera (V), Atalantia buxifolia (A), Citrus ichangensis (I), Citrus medica (M), Citrus grandis (G), Citrus clementine (C), and Citrus sinensis (S). The core eudicot-common hexaploidy is represented by a blue hexagon. (B) Gene tree to show paralogs within each genome, V1,V2, and V3 produced by the ECH, also happened in citrus genomes.

Materials and Methods

Genetic Material

Citrus and grape genome data and their gene annotations were downloaded from the websites respectively, displayed in Supplementary Table 1.

Synonymous Nucleotide Substitutions

Synonymous nucleotide substitutions at synonymous sites (Ks) were estimated by using the Nei-Gojobori approach (Nei and Gojobori, 1986) implemented in the Bioperl Statistical module.

Genomic Homology

BLASTP 2.7.1+ (Altschul et al., 1990) was used to find putative homologous genes (E-value <1e-5, a parameter set to control the similarity between two protein datasets). A loose E-value will not jeopardize the analysis of genomic homology in consideration of divergent evolutionary rates among genes. Credible gene homology will be further supported by gene collinearity, as described later. Genome homology dotplots were produced with a custom in-house program using BLASTP 2.7.1+ results as inputs.

With the putative homologous genes as input information, we ran ColinearScan 1.0.1 to infer collinear genes that help reveal homologous blocks within and between genomes (Wang et al., 2006). Based on similarity (Ks and collinearity gene density) between homologous blocks, we found orthologous and paralogous correspondence between different genomes. Orthologous correspondence shares more collinear genes and smaller Ks values than paralogous correspondence. The correspondence information was used to construct collinear gene tables by filling collinear genes inferred. The collinear gene table was used furthermore to infer gene loss, retention, translocation, etc.

Pseudo-Chromosome Reconstruction

Firstly, we selected the sequences of sweet orange gene to do BLASTN 2.7.1+ searches against scaffolds of citron, papeda, and atalantia, respectively (Altschul et al., 1990). Then, scaffolds were ordered as to their best matched sweet orange genomic segments.

Kernel Function Analysis of Ks

To exhibit the enrichment of Ks, we performed a kernel function analysis of the Ks distribution of collinear genes within a genome or between genomes. With Ks values assumed to follow a normal distribution, Matlab R2014a was adopted to display the distribution of Ks. Then, a curve fitting tool cftool was used to obtain the proper curves by adjusting related parameters, with the popular Gaussian equation. We adjusted the R-square close to 1, the SSE and RMSE as small as possible and the coefficients with 95% confidence bound, and finally determined the goodness of fit.

Evolutionary Dating Correction

Assuming a normal distribution of Ks values, the principle curve was used to represent the corresponding evolutionary event. More detailed methods can be found in our previous publications (Wang et al., 2017a, 2018), with the equations, below, modified due to the lack of an additional polyploidization in citrus plants after the ECH. Considering ECH-related Ks peaks of studied species, we adopted grape as the standard for being the slowest in all studied plants, and corrected the evolutionary rates of the Rutaceae plants. The Maximum likelihood estimate μ can be inferred from the Ks average. Supposing a grape duplicated gene pair to have Ks value that is a random variable XG~(μG,σG2), and for a duplicated gene pair in another genome to have Ks of Xi~(μi,σi2), we determine the relative difference as:

r=(μi-μG)/μG.

To get the corrected Xicorrection ~ (μicorrection, σ2i-correction), we defined the correction coefficient as:

μi-correctionμi=μGμi=λi,

and μi-correction=μGμi×μi=11+r×μi.

λi=11+r

then,

Xi-correction~(λiμi,λi2σi2)

To calculate Ks of homologous gene pairs between two Rutaceae plants, i, j,supposing the Ks distribution is Xij~(μij,σij2), we adopted the algebraic mean of the correction coefficients from two plants,

λij=(λi+λj)/2,

then,

Xij-correction~(λijμij,λij2σij2).

Specifically, when one plant is grape, for the other plant, i, we have,

XiG-correction~(λiμiG,λi2σiG2)

Multiple Sequence Alignment and Evolutionary Tree Construction

The original family genes involved in the Vitamin C pathway in sweet orange were downloaded (http://citrus.hzau.edu.cn/orange/). With these 101 genes as reference, we inferred homologous genes in the other Rutaceae plants and grape (Supplementary Table 2). Then, we combined BLASTP 2.7.1+ (score ≥ 150 and identity ≥ 50%) and HMMER 3.0 (http://hmmer.org/) to refine the inference. Sequences were aligned using Clustal X version 2.0 (Larkin et al., 2007). Phylogenetic trees of the genes involved in the Vitamin C pathway were constructed by using MEGA 7 (the Neighbor-joining method and the Bootstrap value: 1,000) (Kumar et al., 2016) and IQTREE 1.6.8 (default running with all protein test models and the Bootstrap value: 1,000) (Hoang et al., 2017; Kalyaanamoorthy et al., 2017) was used for large families.

Results

Inference of Gene Collinearity Within and Among Genomes

Gene collinearity in extant genomes, describing genes to have preserved ancestral order in ancient genomes, is key to deciphering the complexity of plant genomes and understanding their evolutionary history. Here, we inferred collinear genes within each Rutaceae genome, and between any two of them. Further, we inferred collinear genes in grape, as the outgroup reference, and between grape and each Rutaceae plant. Numbers of homologous blocks containing collinear genes were shown in Supplementary Tables 3, 4. Since citron, papeda and atalantia were assembled only to the scaffold level, we mapped their scaffolds onto sweet orange pseudo-chromosomes to construct their own likely pseudo-chromosomes. These constructed pseudo-chromosomes are helpful in inferring gene collinearity, though they cannot fully reflect the gene content and structure of the actual chromosomes. There are 3,666 to 4,932 collinear genes (Supplementary Table 4) in a genome, forming 2,110 to 2,856 paralogous pairs, inferred from 176 to 307 homologous blocks with 4 or more collinear genes (Supplementary Table 3). The longest homologous block is between pummelo chromosomes Cg5-Cg9, containing 106 gene pairs. For longer blocks with 20 or more genes, fewer collinear genes were inferred in papeda (921 from 5 blocks) and citron (721 from 2 blocks) possibly due to poor assembly (Supplementary Tables 3, 4). Comparatively, grape has 176 blocks (including 2,116 gene pairs formed by 3,666 genes), fewer than those within a Rutaceae genome (Supplementary Tables 3, 4).

The collinearity between genomes (intergenomic) is higher (more conserved) than within a genome (intragenomic), consistent with speciation following genome duplication and showing well-preserved ancestral Rutaceae, even eudicot, genome structure in extant plants. As to blocks with 4 or more genes, sweet orange has 3,792 collinear genes within its genome and shares 10,342–14,120 collinear genes with other citrus genomes (Supplementary Table 4). Even with atalantia and grape, sweet orange shares 12,789 and 9,108 collinear genes, respectively, much more than its intragenomic collinear gene number. The longest block between citrus and grape is located between citrus chromosome 3 and grape chromosome 18, while the longest block appears between atalantia chromosome 5 and grape chromosome 7. Apparently, clementine and pummelo have the best collinearity, involving 15,716 (64.52%) and 15,474 (55.18%) genes, respectively. Notably, the longest homologous block appeared between pummelo and clementine with 1,356 genes. Similarly, sweet orange has the second longest homologous block with clementine, involving 1,328 collinear genes (Supplementary Table 4).

More specific statistics regarding orthologous, paralogous and outparalogous genes, gene pairs and gene blocks were displayed in Supplementary Tables 3, 4.

Distinguishing Orthology From Outparalogy

Here, we used the grape genome to distinguish orthologous and outparalogous regions between different genomes. Without considering lineage-specific gene losses or duplications, we would expect that a grape gene (or chromosomal region) had one best matched or orthologous Rutaceae gene (chromosomal region), and two secondary or outparalogous genes (chromosomal regions). Specifically, we illustrated the principle with three grape chromosomes (Vv6, Vv8, and Vv13), being ECH-produced homoeologs/paralogs (Jaillon et al., 2007; Jiao et al., 2011; Wang et al., 2017a), to find their respective orthologous and outparalogous regions in the sweet orange (Cs) genome (Supplemental Figure S1). As to gene collinearity and sequence divergence (measured by using synonymous nucleotide substitution rates, or Ks), Vv6 is orthologous to most of Cs8 (including 347 collinear genes with median Ks = 0.92), and complemented by several smaller fragments in Cs1, Cs2, Cs3, Cs6, and Cs9 (including 8, 92, 21, 21, and 40 collinear genes, respectively), while Vv8 and Vv 13 are mainly orthologous to Cs6 (514 collinear genes with Ks = 0.88) and Cs7 (446 collinear genes with Ks = 0.935), respectively complemented by fragments from other grape chromosomes. Non-orthologous alternative correspondence means outparalogy, often having fewer or extensively diverged collinear genes. For example, for outparalogous correspondence, Vv6-Cs3 share only 5 collinear genes and Vv6-Cs5 share 6 collinear genes; though Vv6-Cs6 share 90 collinear genes, far fewer than Vv6-Cs8 (347) and much more diverged (Ks = 0.93). Likewise, Vv8 and Vv13 also had a similar phenomenon, with orthologous regions much better preserved than outparalogous regions.

Eventually, we managed to distinguish orthologous and outparalogous regions between grape and each Rutaceae plant, and similarly we inferred orthologous and outparalogous regions between any two Rutaceae plants.

Table 1 summarizes the number of duplicate genes in relation to the ECH. In grape, 1,289 paralogous gene pairs, involving 2,364 extant genes, were inferred to be produced by the ECH, accounting for 54.53% of all inferred collinear genes. In citrus genomes, clementine has 1,817 ECH-produced gene pairs (3,368 genes) from 86 blocks; sweet orange has 962 gene pairs (1,850 genes) from 54 blocks; pummelo has 1,402 gene pairs (2,604 genes) from 77 blocks, and citron and papeda has 39 paralogous blocks (471 gene pairs with 943 genes) and 43 paralogous blocks (443 gene pairs with 853 genes). The citrus relative, atalantia has 54 paralogous blocks with 790 gene pairs and 1,511 genes.

TABLE 1
www.frontiersin.org

Table 1. Number of duplicated genes within a genome related to the ECH.

The reason why the paralogous genes of citron, papeda, and atalantia appear to retain fewer ECH-related collinear genes is likely the unfinished positioning of the genes to chromosomes and relatively poor assembly.

Multiple Genome Alignment and Genomic Fractionation

To explore genome structural changes in the Rutaceae, using the above-distinguished orthology and outparalogy between genomes, we built multiple genome alignments represented with a table of orthologous and paralogous genes (Supplementary Table 5). In the table, 21 columns can be divided into three collinear gene groups (7 × 3 = 21), corresponding to tripled genes in the ECH. The first column is filled with grape gene IDs (24,283 ones) in their chromosomal order and chromosome by chromosome, and the following six columns are assigned to each of the six studied Rutaceae plants for each collinear gene group. In each column, a cell is filled with a collinear gene ID, or a dot meaning no inferred collinear correspondence. Within each group, the collinear genes in the compared genomes are orthologous, while the relationship of collinear genes between groups can be classified into two types, paralogous genes within the same species and outparalogous ones between different species. We showed the collinearity among these compared species in Supplementary Figure S2.

Based on the homology table, we characterized genomic fractionation in each Rutaceae genome after its divergence from grape. With grape as the reference, we found 69 fragments (8,249 genes, 34.05% of the total) within sweet orange (Figure 2), 71 (9,670 genes, 39.91%) within clementine, and 71 (9,086 genes, 37.50%) within pummelo (Table 2). Using the constructed pseudo-chromosomes of three other Rutaceae plants, we inferred 72 fragments (5,341 genes, 22.04% of the total) within papeda, 77 (4,689 genes, 19.35%) within citron, and 82 (6,309 genes, 26.04%) within atalantia (Table 2). These findings show large-scale genomic fragmentation in Rutaceae plants (Supplementary Table 6). Additionally, we found that Rutaceae plants shared 87% (60 fragments) of collinear segments and breakage points with grape chromosomes, with sweet orange having the lowest (Figure 2), showing that most of the chromosomal rearrangement occurred before their divergence.

FIGURE 2
www.frontiersin.org

Figure 2. Genome homology between grape (V) and sweet orange (C). Best-matched genes from two genomes are colored in red, secondary matches in blue, and others in gray. The 19 grape chromosomes are shown in 7 colors, corresponding to their 7 ancestral proto-chromosomes before the ECH. Orthologous blocks were identified by solid-line rectangles. Bi-directional arrows link complementary correspondence showing inferred chromosome breakages during evolution of sweet orange.

TABLE 2
www.frontiersin.org

Table 2. Orthologous genes in citrus and their relative with grape as reference.

Gene collinearity due to gene loss and translocation before the radiation of the Rutaceae lineage was examined using sweet orange as the reference (Supplementary Table 7), with its 23,582 genes related to their orthologs and outparalogs from other Rutaceae plants, and paralogs in sweet orange itself. The lineage-specific gene content and genomic structural changes after the radiation of Rutaceae plants are illustrated in Supplemental Figure S3 with sweet orange as the outgroup. We counted the collinear genes with sweet orange as the reference–9 sweet orange chromosomes (23,582 genes) were mapped with 58 collinear fragments (13,848 genes, 58.72% of the total) in clementine; 85 (14,236 genes, 60.37% of the total) in pummelo; 49 (10,205 genes, 43.27% of the total) in citron; 68 (11,715 genes, 49.68%) in papeda; and 37 (12,643 genes, 53.61%) in atalantia (Table 3 and Supplementary Table 8). For example, sweet orange chromosome 1 was mapped with eight fragments in clementine; with two fragments each mapped to chromosomes 4 and 5, with three fragments each to chromosomes 1 and 3, with one fragment to chromosome 1 fragment being inverted.

TABLE 3
www.frontiersin.org

Table 3. Orthologous genes in citrus and their relative with sweet orange as reference.

Gene Loss and Retention

To better explain the collinearity in citrus genomes, we selected a partial segment of multiple gnome alignments to exhibit gene content changes (Supplementary Figure S4). Aligned homologous regions were selected from grape chromosomes 14, 1, and 17, best-matched/orthologous to local regions of Rutaceae chromosomes 6, 7 and 5, respectively. A region of 0.75 Mb on grape chromosome 14 (from 29.55 to 30.25 Mb) shares an appreciable number of orthologous genes (70 genes) with sweet orange chromosome 6 (31 genes, 20.52–20.96 Mb), the orthologous region in clementine chromosome 6 (31 genes, 24.92–25.39 Mb) and the orthologous region in pummelo chromosome 6 (29 genes, 23.07–23.50 Mb). Unlike the former ones, the above region on grape chromosome 14 shares a relatively short fragment on citron chromosome 6 (17 genes, 37.53–37.82 Mb), a dispersed orthology in atalantia (38 genes, 49.52–50.76 Mb) and papeda (30 genes, 42.12–42.60 Mb).

The first group taking grape chromosome 14 as the reference showed a higher collinear gene density than the other two groups of outparalogs that were more dispersed. In the second group of local alignments, the long region on grape chromosomes 1 (11.01–12.39 Mb) aligned with chromosome 7 in citrus and their relative, specifically located on sweet orange (12 genes, 1.62–2.11 Mb), clementine (11 genes, 23.62-24.03 Mb), pummelo (11 genes, 20.40-20.80 Mb), citron (8 genes, 5.31–5.64 Mb), papeda (9 genes, 2.51–3.35 Mb), and atalantia (8 genes, 23.41–23.78 Mb).

The last group of homologous regions produced by ECH showed a relatively regular alignment, with the region on grape chromosome 17 (6.17–6.61 Mb) corresponding to the regions on chromosome 5 (7 collinear genes located) in Rutaceae plants in a region about 2–6 Mb (7–9 genes) apparently located at the end of the chromosome. More detailed information about the local alignment among the compared species is displayed in Supplementary Figure S4.

Genomic fragmentation was accompanied by wide-spread gene losses or translocations. Using the grape genome as a reference, 37.5%-80.6% of genes were retained as collinear orthologs. For example, using grape chromosome 1 as outgroup, 65.2, 84.7, and 78.4% grape genes were found to have collinear counterparts in sweet orange, clementine, and pummelo, respectively (Supplementary Table 9). The other three Rutaceae plants have lower gene retention rates likely due to poor assembly. To better display the scale of gene retention, we depicted the retained genes within Rutaceae plants after the divergence with grape (Supplementary Figures S5, S6.)

To investigate potential mechanisms of genomic fractionation, we counted the number of removed genes (due to gene deletion or translocation) in each Rutaceae genome. We inferred that 3,765 genes were removed from the orthologous regions in sweet orange; and similar numbers were detected in other plants (4,221 in clementine, 4,143 in pummelo, 2,580 in citron, 2,788 in papeda, and 3,139 in atalantia). By checking the gap sizes between neighboring genes in collinearity, we found that most (87–96%) gene removal events involved 15 or fewer genes, with the majority of removals involving one or two genes in an event. A statistical fitness regression showed that gene removal patterns largely followed a geometric distribution (geometric parameter 0.4676–0.5396 and goodness of fit F-test p-value 0.8852–0.9356 to accept the fitness) (Figure 3). For example, we inferred that 10.22% (2,409) DNA fractionation events are small in scale, removing 1 or 2 genes at one time, and responsible for 63.98% of the removed (3,765) genes in sweet orange.

FIGURE 3
www.frontiersin.org

Figure 3. Near geometric distribution of continually lost or translocated genes between grape and Rutaceae plants. Vitis vinifera was compared to 5 citrus (Citrus sinensis, Citrus clementine, Citrus grandis, Citrus medica, and Citrus ichangensis) and one relative, Atalantia buxifolia. The x-axis represents numbers of continually lost or translocated genes in the inferred homologous regions. The y-axis represents the number of removed genes.

We also characterized gene loss and retention in Rutaceae plants with sweet orange as the reference (Supplementary Figures S7, S8). Compared to sweet orange, 76.0–82.6% orthologous genes were retained in clementine, and similar numbers in pummelo (78.6–84.2%). Much lower inferred retention rates in citron (52.2–67.6%), papeda (60.6–76.6%), and atalantia (61.6–79.6%) may be the result of insufficient genome assemblies (Supplementary Table 10). The number of continually removed genes in the other Rutaceae plants also approximately followed a geometric distribution, with parameters from 0.5991 to 0.6661, fitness values from 0.9908 to 0.9986, and p-values (F-test) from 0.9093 to 0.9635 (Supplementary Table 11). Events removing 1 or 2 genes accounted for most removal events [clmentine (77.30%), pummelo (79.82%), citron (70.16%), papeda (65.55%), and atalantia (74.43%)].

Evolutionary Divergence and Dating

By inferring Ks between paralogous and orthologous genes in collinearity, we estimated divergence time among Rutaceae plants. We found that the ECH Ks distributions in different Rutaceae plants had peak locations ranging from 1.252–1.301, with papeda at Ks = 1.252 (±0.343), and sweet orange at Ks = 1.301 (±0.343). This shows a <5% difference in evolutionary rates among Rutaceae plants. By contrast, Rutaceae plants evolved faster (18.90–23.55%) than grape with Ks peak of its paralogs at 1.053 (±0.29) (Supplementary Table 12 and Figure 4). Using grape as the reference, we aligned the Rutaceae Ks peaks to its peak and performed an evolutionary rate correction (See Methods for details). Then, using the corrected Ks, we assessed evolutionary dates of speciation events. The Ks peak of grape-Rutaceae orthologs was 0.744(±0.21). Assuming that the ECH occurred ~115–130 mya, the split of Rutaceae from grape and other eudicots was inferred to be 81.15–91.74 mya (Supplementary Table 13 and Figure 4). Rutaceae plants radiated <10 mya. For example, Atalantia buxifolia, belonging to the genus related to citrus, the divergent node with citrus appeared at 5.6–6.4 mya, while the remaining species split within the last 2 million years. Especially recent was the divergence time between sweet orange and clementine (1.1–1.2 mya), and pummelo and clementine (1.8–2.1 mya).

FIGURE 4
www.frontiersin.org

Figure 4. Dating evolutionary events within and among Rutaceae genomes. Distributions of Ks between intragenomic collinear genes are shown with solid curves and intergenomic ones with dashed curves. (A) Distributions before Ks correction. (B1,2) and (C1,2). Distributions of Ks after correction. Inferred times are shown beneath Time-axis.

Vitamin C Synthesis

We investigated how the ECH affected the copy number variation of genes involved in the biosynthesis of vitamin C. Using previously reported genes related to the biosynthesis of sweet orange vitamin C as seeds (Xu et al., 2013), we found their homologous genes in Rutaceae genomes with Blastp E-value <1e-5, score >150 and identity ≥50 (Altschul et al., 1990) (Supplementary Table 14). We identified total numbers of vitamin C gene homologs in Rutaceae plants ranging from 101 (sweet orange) to 143 (papeda). In grape, 53.39% (63) of vitamin gene homologs are ECH-related, showing that polyploidization increased vitamin C gene copy numbers. In citron (26 genes, 23.01%) and papeda (31, 24.41%), relatively smaller percentages of vitamin C genes are ECH-related, possibly underestimated due to incomplete genome assembly. For example, L-ascorbate peroxidase (APX) involves 4 ECH-related copies in every Rutaceae plant. The biggest subfamily, Putative pectinesterase/pectinesterase inhibitor (PME), has 35 genes in clementine, and 10 copies are ECH-related (~29%). The subfamilies, L-galactono-1,4-lactone dehydrogenase (GLOase) and L-galactono-1,4-lactone dehydrogenase (GalLDH) have no genes clearly related to ECH in Rutaceae plants, while in grape, they have ECH-related copies (Supplementary Table 14).

We constructed phylogenetic gene trees to help understand the evolution of genes involved in the biosynthesis of vitamin C. The trees displayed complicated relationships just like their ambiguous hybrid relationships among these compared Rutaceae plants (Supplementary Figures S9, S10). Here we show a gene tree of the subfamily within the Vitamin C pathway, nucleobase-ascorbate transporter (AAT) (Figure 5). The genes can be divided into several groups, and we selected 6 larger groups marked B1-B6. From B6, taking grape genes as an outgroup, we observed that the relationship of genes Vv10g21237- Ab2g28191- Ci2g041190- Cm2g243340- Cg2g043510- Cs2g0680- Cc2g02861 basically agrees with the phylogenetic tree of plants. We have to note that subtrees formed by Rutaceae genes displayed complex relationships among these plants, especially between citron and “the triangle” among sweet orange (Cs), clementine mandarin (Cc), and pummelo (Cg). Since the genetic hybridization within “the triangle,” the three citrus plants tend to run faster than the wild citrus, citron (Cm), which made certain subtrees inconsistent with their evolutionary relationship (Figure 5). More specific information is displayed in Supplementary Figures S9, S10.

FIGURE 5
www.frontiersin.org

Figure 5. Gene tree of Vitamin C related genes. The nucleobase-ascorbate transporter (AAT) gene family including 61 homologous copies in grape and Rutaceae plants was constructed. Numbers displayed in the nodes represent the percent bootstrap from 1,000 repetitions.

Discussion

Genome Fractionation

Polyploidization, at the whole genome level, increased gene content, subsequently even immediately followed by enormous genomic changes, e.g., chromosome fragmentation and/or rearrangement, potential gene deletion or relocation, gene mutation and origination of novel genes (Soltis and Soltis, 1999; Blomme et al., 2006; Soltis et al., 2009; Sankoff and Zheng, 2012). Comparing six Rutaceae plants and grape (preserving a relatively complete genome comparing with the ECH), we found frequent fractionations and rearrangements. That is, these Rutaceae genomes suffered appreciable changes after the divergence with grape. Unlike other extant plants that have experienced multiple rounds of polyploidization, Rutaceae have instead hybridized with their relatives since the ECH over 100 million years ago. The hybridization may also contribute to genome fractionation due to homologous recombination.

High Gene Retention Rate in Rutaceae

Large scale gene losses have been ascribed to polyploidization (Bowers et al., 2003; Town et al., 2006; Schnable et al., 2012), and previous studies found a gene loss rate of 70% within the cotton genome after decaploidy, showing genomic instability (Wang et al., 2016). Redundant copies of genes after polyploidization are often removed from the genome by fractionation (Langham et al., 2004; Schnable et al., 2012). However, with obvious deviation from a random distribution, gene losses could be more complex. Rutaceae plants may have suffered by recursive gene losses accompanied by fractionation, and the ongoing manner of gene loss appeared in extant species was reported (Scannell et al., 2006; Swanson-Wagner et al., 2010; Woodhouse et al., 2010). In this study, we found that the better assembled Rutaceae genomes had collinear gene retention rates up to 65% or more. Comparatively, plants with extra rounds of polyploidization tended to have less gene retention, e.g., upon to 31% in soybean, which was affected by two additional tetraploidization events after the ECH (Wang et al., 2017a), and 58.4% in watermelon, affected by one additional tetraploidization (Wang et al., 2018).

Divergent Evolutionary Rates

Considering the controversial origins of Rutaceae plants, we selected duplicated genes produced by polyploidization within a genome, or collinear orthologous genes between two different species, to deduce their evolutionary rates. Plants often evolve at very divergent rates. A previous study in cucurbits, using the above mentioned approach, proved that melon is the slowest at evolving, with watermelon and cucumber faster by 23.6 and 27.4% (Wang et al., 2018). Likewise with legumes, lotus evolves the slowest and peanut was nearly 25% faster (Wang et al., 2017a). The studied homologous blocks and the collinear genes residing in them are almost sure to have originated simultaneously, providing a good opportunity to evaluate divergent evolutionary rates among genomes. Here, with ECH-related duplicated genes in Rutaceae plants, we found Rutaceae plants varying by <5% in their evolutionary rates, and showing a 19–24% faster rate than grape. Divergent evolutionary rates may be related to their ecological niche, and their different evolutionary history. The actual biological mechanisms responsible for divergent evolutionary rates remain to be identified.

Data Availability

The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.

Author Contributions

XW and JW: conceptualization. JYuan and JW: formal analysis. JYu, FM, YZ, JL, PS, SSu, ZZ, CL, CW, HG, XL, XD, SSh, YX, YH, JZ, and TS: formal analysis. JYuan: data curation. JYuan and JW: writing—original draft. XW: writing—review and editing. XW: supervision.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We appreciate financial support from the Ministry of Science and Technology of the People's Republic of China (2016YFD0101001), China National Science Foundation (31510333 to JW and 3117022 to XW), Natural Science Foundation of Hebei Province (C2015209069 to JW), and the Graduate Student Innovation Fund of North China University of Science and Technology (2018S42 to JYuan). We thank the helpful discussion with researchers at the iGeno Co. Ltd., China. Requests for materials and home-made tools should be addressed to the corresponding author.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2019.00986/full#supplementary-material

References

Adams, K. L., and Wendel, J. F. (2005). Polyploidy and genome evolution in plants. Curr. Opin. Plant Biol. 8, 135–141. doi: 10.1016/j.pbi.2005.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Altschul, S. F., Gish, W., Miller, W., Myers, E. W., and Lipman, D. J. (1990). Basic local alignment search tool. J. Mol. Biol. 215, 403–410. doi: 10.1016/S0022-2836(05)80360-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Aury, J. M., Jaillon, O., Duret, L., Noel, B., Jubin, C., Porcel, B. M., et al. (2006). Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia. Nature 444, 171–178. doi: 10.1038/nature05230

PubMed Abstract | CrossRef Full Text | Google Scholar

Barrett, H. C., and Rhodes, A. M. (1976). A numerical taxonomic study of affinity relationships in cultivated citrus and its close relatives. System. Bot. 1, 105–136. doi: 10.2307/2418763

CrossRef Full Text | Google Scholar

Blomme, T., Vandepoele, K., De Bodt, S., Simillion, C., Maere, S., and Peer, Y. V. D. (2006). The gain and loss of genes during 600 million years of vertebrate evolution. Genome Biol. 7:R43. doi: 10.1186/gb-2006-7-5-r43

PubMed Abstract | CrossRef Full Text | Google Scholar

Bowers, J. E., Chapman, B., Rong, J., and Paterson, A. H. (2003). Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events. Nature 422, 433–438. doi: 10.1038/nature01521

PubMed Abstract | CrossRef Full Text | Google Scholar

Buggs, R. J., Chamala, S., Wu, W., Tate, J. A., Schnable, P. S., Soltis, D. E., et al. (2012). Rapid, repeated, and clustered loss of duplicate genes in allopolyploid plant populations of independent origin. Curr. Biol. 22, 248–252. doi: 10.1016/j.cub.2011.12.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheong, M. W., Liu, S. Q., Zhou, W., Curran, P., and Yu, B. (2012). Chemical composition and sensory profile of pomelo (Citrus grandis (L.) Osbeck) juice. Food Chem. 135, 2505–2513. doi: 10.1016/j.foodchem.2012.07.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Curk, F., Ollitrault, F., Garcia-Lor, A., Luro, F., Navarro, L., and Ollitrault, P. (2016). Phylogenetic origin of limes and lemons revealed by cytoplasmic and nuclear markers. Ann. Bot. 117, 565–583. doi: 10.1093/aob/mcw005

PubMed Abstract | CrossRef Full Text | Google Scholar

Freeling, M., Lyons, E., Pedersen, B., Alam, M., Ming, R., and Lisch, D. (2008). Many or most genes in Arabidopsis transposed after the origin of the order Brassicales. Genome Res. 18, 1924–1937. doi: 10.1101/gr.081026.108

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoang, D. T., Chernomor, O., Von, H. A., Minh, B. Q., and Le, S. V. (2017). UFBoot2: improving the ultrafast bootstrap approximation. Mol. Biol. Evol. 35, 518–522. doi: 10.1093/molbev/msx281

PubMed Abstract | CrossRef Full Text | Google Scholar

Jaillon, O., Aury, J. M., Noel, B., Policriti, A., Clepet, C., Casagrande, A., et al. (2007). The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla. Nature 449, 463–467. doi: 10.1038/nature06148

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiao, Y., Wickett, N. J., Ayyampalayam, S., Chanderbali, A. S., Landherr, L., Ralph, P. E., et al. (2011). Ancestral polyploidy in seed plants and angiosperms. Nature 473, 97–100. doi: 10.1038/nature09916

PubMed Abstract | CrossRef Full Text | Google Scholar

Kalyaanamoorthy, S., Minh, B. Q., Tkf, W., Von, H. A., and Jermiin, L. S. (2017). ModelFinder: fast model selection for accurate phylogenetic estimates. Nat. Methods 14:6. doi: 10.1038/nmeth.4285

PubMed Abstract | CrossRef Full Text | Google Scholar

Kumar, S., Stecher, G., and Tamura, K. (2016). MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33, 1870–1874. doi: 10.1093/molbev/msw054

PubMed Abstract | CrossRef Full Text | Google Scholar

Langham, R. J., Justine, W., Molly, D., Cynthia, K., Goff, S. A., and Michael, F. (2004). Genomic duplication, fractionation and the origin of regulatory novelty. Genetics 166, 935–945. doi: 10.1534/genetics.166.2.935

PubMed Abstract | CrossRef Full Text | Google Scholar

Larkin, M. A., Blackshields, G., Brown, N. P., Chenna, R., Mcgettigan, P. A., Mcwilliam, H., et al. (2007). Clustal W and Clustal X version 2.0. Bioinformatics 23, 2947–2949. doi: 10.1093/bioinformatics/btm404

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y. Q., Heying, E., and Tanumihardjo, S. A. (2012). History, global distribution, and nutritional importance of citrus fruits. Compr. Rev. Food Sci. Food Safe. 11, 530–544. doi: 10.1111/j.1541-4337.2012.00201.x

CrossRef Full Text | Google Scholar

Maere, S., Bodt, S. D., Raes, J., Casneuf, T., Montagu, M. V., Kuiper, M., et al. (2005). Modeling gene and genome duplications in eukaryotes. Proc. Natl. Acad. Sci. U.S.A. 102, 5454–5459. doi: 10.1073/pnas.0501102102

PubMed Abstract | CrossRef Full Text | Google Scholar

Moore, G. A. (2001). Oranges and lemons: clues to the taxonomy of Citrus from molecular markers. Trends Genet. 17, 536–540. doi: 10.1016/S0168-9525(01)02442-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Nei, M., and Gojobori, T. (1986). Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol. Biol. Evol. 3, 418–426.

PubMed Abstract | Google Scholar

Nicolosi, E., Deng, Z. N., Gentile, A., Malfa, S. L., Continella, G., and Tribulato, E. (2000). Citrus phylogeny and genetic origin of important species as investigated by molecular markers. Theor. Appl. Genet. 100, 1155–1166. doi: 10.1007/s001220051419

CrossRef Full Text | Google Scholar

Sankoff, D., and Zheng, C. (2012). Fractionation, rearrangement and subgenome dominance. Bioinformatics 28, i402–8. doi: 10.1093/bioinformatics/bts392

PubMed Abstract | CrossRef Full Text | Google Scholar

Scannell, D. R., and Byrne, K.P.L.G.J. (2006). Multiple rounds of speciation associated with reciprocal gene loss in polyploid yeasts. Nature 440, 341–345. doi: 10.1038/nature04562

PubMed Abstract | CrossRef Full Text | Google Scholar

Schnable, J. C., Freeling, M., and Lyons, E. (2012). Genome-wide analysis of syntenic gene deletion in the grasses. Genome Biol. Evol. 4, 265–277. doi: 10.1093/gbe/evs009

PubMed Abstract | CrossRef Full Text | Google Scholar

Scora, R. W. (1975). On the history and origin of citrus. Bull. Torrey Bot. Club 102, 369–375. doi: 10.2307/2484763

CrossRef Full Text | Google Scholar

Singh, A., Maurya, S., and Singh, U. P. (2014). Chromatographic analysis of phenolic acids in the fruit pulp of some citrus varieties and their therapeutic importance in human health. Int. Annal. Adv. Sci. Res. 1, 150–154.

Google Scholar

Soltis, D. E., Albert, V. A., LeebensMack, J., Bell, C. D., Paterson, A. H., Zheng, C., et al. (2009). Polyploidy and angiosperm diversification. Am. J. Bot. 96, 336–348. doi: 10.3732/ajb.0800079

PubMed Abstract | CrossRef Full Text | Google Scholar

Soltis, D. E., and Soltis, P. S. (1999). Polyploidy: recurrent formation and genome evolution. Trends Ecol. Evol. 14, 348–352. doi: 10.1016/S0169-5347(99)01638-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Swanson-Wagner, R. A., and Eichten SR, S.K. (2010). Pervasive gene content variation and copy number variation in maize and its undomesticated progenitor. Genome Res. 20, 1689–1699. doi: 10.1101/gr.109165.110

PubMed Abstract | CrossRef Full Text | Google Scholar

Talon, M., and Gmitter, F. G. Jr. (2008). Citrus genomics. Int. J. Plant Genom. 2008, 1–17. doi: 10.1155/2008/528361

PubMed Abstract | CrossRef Full Text | Google Scholar

The Arabidopsis Genome Initiative (2000). Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408, 796–815. doi: 10.1038/35048692

CrossRef Full Text | Google Scholar

Town, C. D., Foo, C., Rama, M., Jonathan, C., Haas, B. J., Wortman, J. R., et al. (2006). Comparative genomics of Brassica oleracea and Arabidopsis thaliana reveal gene loss, fragmentation, and dispersal after polyploidy. Plant Cell 18, 1348–1359. doi: 10.1105/tpc.106.041665

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Sun, P., Li, Y., Liu, Y., Yang, N., Yu, J., et al. (2018). An overlooked paleo-tetraploidization in Cucurbitaceae. Mol. Biol. Evol. 35:242. doi: 10.1093/molbev/msx242

CrossRef Full Text | Google Scholar

Wang, J., Sun, P., Li, Y., Liu, Y., Yu, J., Ma, X., et al. (2017a). Hierarchically aligning 10 legume genomes establishes a family-level genomics platform. Plant Physiol. 174, 284–300. doi: 10.1104/pp.16.01981

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Guo, H., Wang, J., Lei, T., Liu, T., Wang, Z., et al. (2016). Comparative genomic de-convolution of the cotton genome revealed a decaploid ancestor and widespread chromosomal fractionation. New Phytol. 209, 1252–1263. doi: 10.1111/nph.13689

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Shi, X., Hao, B., Ge, S., and Luo, J. (2005). Duplication and DNA segmental loss in the rice genome: implications for diploidization. New Phytol. 165, 937–946. doi: 10.1111/j.1469-8137.2004.01293.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Shi, X., Li, Z., Zhu, Q., Kong, L., Tang, W., et al. (2006). Statistical inference of chromosomal homology based on gene colinearity and applications to Arabidopsis and rice. BMC Bioinform. 7:447. doi: 10.1186/1471-2105-7-447

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Xu, Y., Zhang, S., Li, C., Huang, Y., Cheng, J., et al. (2017b). Genomic analyses of primitive, wild and cultivated citrus provide insights into asexual reproduction. Nat. Genet. 49, 765–773. doi: 10.1038/ng.3839

PubMed Abstract | CrossRef Full Text | Google Scholar

Woodhouse, M. R., Schnable, J. C., and Pedersen, B. S. (2010). Following tetraploidy in maize, a short deletion mechanism removed genes preferentially from one of the two homeologs. PLoS Biol. 8:e1000409. doi: 10.1371/journal.pbio.1000409

CrossRef Full Text | Google Scholar

Wu, G. A., Prochnik, S., Jenkins, J., Salse, J., Hellsten, U., Murat, F., et al. (2014). Sequencing of diverse mandarin, pummelo and orange genomes reveals complex history of admixture during citrus domestication. Nat. Biotechnol. 32, 656–662. doi: 10.1038/nbt.2906

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, G. A., Terol, J., Ibanez, V., López-García, A., Pérez-Román, E., Borredá, C., et al. (2018). Genomics of the origin and evolution of Citrus. Nature 554, 311–317. doi: 10.1038/nature25447

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, Q., Chen, L. L., Ruan, X., Chen, D., Zhu, A., Chen, C., et al. (2013). The draft genome of sweet orange (Citrus sinensis). Nat. Genet. 45, 59–66. doi: 10.1038/ng.2472

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: rutaceae, whole-genome duplication, genome alignment, gene collinearity, duplicated genes, genome fractionation

Citation: Yuan J, Wang J, Yu J, Meng F, Zhao Y, Li J, Sun P, Sun S, Zhang Z, Liu C, Wei C, Guo H, Li X, Duan X, Shen S, Xie Y, Hou Y, Zhang J, Shehzad T and Wang X (2019) Alignment of Rutaceae Genomes Reveals Lower Genome Fractionation Level Than Eudicot Genomes Affected by Extra Polyploidization. Front. Plant Sci. 10:986. doi: 10.3389/fpls.2019.00986

Received: 04 April 2019; Accepted: 12 July 2019;
Published: 06 August 2019.

Edited by:

Michael Eric Schranz, Wageningen University & Research, Netherlands

Reviewed by:

Liangsheng Zhang, Fujian Agriculture and Forestry University, China
Eric Wade Linton, Central Michigan University, United States

Copyright © 2019 Yuan, Wang, Yu, Meng, Zhao, Li, Sun, Sun, Zhang, Liu, Wei, Guo, Li, Duan, Shen, Xie, Hou, Zhang, Shehzad and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Tariq Shehzad, shehzad@uga.edu; Xiyin Wang, wangxiyin@vip.sina.com

These authors have contributed equally to this work