Abstract
Actinidia chinensis is an important economic plant belonging to the basal lineage of the asterids. Availability of a complete Actinidia chloroplast genome sequence is crucial to understanding phylogenetic relationships among major lineages of angiosperms and facilitates kiwifruit genetic improvement. We report here the complete nucleotide sequences of the chloroplast genomes for Actinidia chinensis and A. chinensis var deliciosa obtained through de novo assembly of Illumina paired-end reads produced by total DNA sequencing. The total genome size ranges from 155,446 to 157,557 bp, with an inverted repeat (IR) of 24,013 to 24,391 bp, a large single copy region (LSC) of 87,984 to 88,337 bp and a small single copy region (SSC) of 20,332 to 20,336 bp. The genome encodes 113 different genes, including 79 unique protein-coding genes, 30 tRNA genes and 4 ribosomal RNA genes, with 16 duplicated in the inverted repeats, and a tRNA gene (trnfM-CAU) duplicated once in the LSC region. Comparisons of IR boundaries among four asterid species showed that IR/LSC borders were extended into the 5’ portion of the psbA gene and IR contraction occurred in Actinidia. The clap gene has been lost from the chloroplast genome in Actinidia, and may have been transferred to the nucleus during chloroplast evolution. Twenty-seven polymorphic simple sequence repeat (SSR) loci were identified in the Actinidia chloroplast genome. Maximum parsimony analyses of a 72-gene, 16 taxa angiosperm dataset strongly support the placement of Actinidiaceae in Ericales within the basal asterids.
Introduction
In plants, chloroplasts (cp) are key organelles for photosynthesis and are crucial in the biosynthesis of starch, fatty acids, pigments and amino acids [1]. Typically, cp genomes in angiosperms are highly conserved and have circular genomes ranging from 115 to 165 kb in length and consisting of a large-single-copy region (LSC; 80–90 kb) and a small-single-copy region (SSC; 16–27 kb), separated by an inverted repeat (IR) [2,3]. In contrast to nuclear and mitochondrial genomes, chloroplast genomes are largely conserved in gene content, organization and structure [3]. However, mutations, duplications, losses and rearrangements of genes have been observed in several angiosperm lineages [4].
Complete plastid genome sequences of vascular plants were first reported in tobacco [5]. Advances in next-generation sequencing technologies have enabled the rapid acquisition of whole cp genome sequences at low cost. At present, over 600 cp genome sequences are currently deposited at the National Center for Biotechnology Information (NCBI) including all of the major lineages of the plant kingdom. To date, only three complete cp genomes have been sequenced for representatives of the basal asterids: Ardisia polysticta (Myrsinaceae) [6], Camellia sinensis (Theaceae) [7], and Vaccinium macrocarpon (Ericaceae) [8]. More cp genome sequences from additional taxa of the basal asterids are needed for understanding phylogenetic relationships among angiosperms [7].
Kiwifruit is an important fruit tree in the Actinidiaceae family of the asterids. This family includes 3 genera, i.e., Actinidia, Clematoclethra and Saurauia [9]. Actinidia, comprising 74 species, is widely distributed in Eastern Asia from just south of the Equator in the tropics to cold temperate regions as far north as 50° latitude [10]. Actinidia chinensis and A. chinensis var deliciosa, from which most commercial kiwifruit varieties have been developed, have received considerable attention over the last forty years [10,11].
As an important crop plant grown for fresh fruit, kiwifruit is cultivated in 14 countries. The world kiwifruit acreage was 166,000 hectares and annual kiwifruit production was around 2 million metric tons in 2012 [12]. Bacterial canker of kiwifruit, caused by Pseudomonas syringae pv. actinidiae (Psa), is currently the major cause of losses in kiwifruit production worldwide [13]. As an environmentally friendly approach, genetic engineering would be very useful to develop a method of disease resistance to Psa. Compared to nuclear genome engineering, chloroplast genetic engineering often gives high expression levels [14,15], which holds great promise for breeding kiwifruit cultivars with disease resistance. However, the lack of complete chloroplast genome sequences is one of the major limitations of extending this technology to most crops [15]. Hence, complete chloroplast genome sequences of kiwifruit are needed.
For the last three decades, numerous phylogenetic studies using chloroplast DNA sequence data have contributed to our understanding of the evolutionary relationships within the genus [16,17]. However, the interspecies relationships within the genus Actinidia remain largely controversial [10]. With the goal of developing molecular markers for further understanding phylogenetic relationships in Actinidia and chloroplast genome evolution in asterids, here we report the complete chloroplast genome sequences of A. chinensis and A. chinensis var deliciosa, the first cp genomes for the Actinidiaceae, obtained through de novo assembly of IIIlumina paired-end reads and produced by total DNA sequencing. Information on the complete chloroplast genome sequence will be instrumental for genetic engineering and breeding programs.
Materials and Methods
Plant materials
The genus Actinidia contains extensive natural ploidy variation with species known at four ploidy levels (diploid through octoploid). Four individuals, representing three ploidy levels of the Actinidia chinensis complex, including A. chinensis var. chinensis (2×) (accession number AC011), A. chinensis var. chinensis (4×) (accession number AC017), A. chinensis var deliciosa (4×) (accession number AD006) and A. chinensis var deliciosa (6×) (accession number AD019), were received from the National Actinidia Germplasm Repository of China (Wuhan, China). Approximately 100 g young leaf tissue per individual was harvested for extraction of genomic DNA.
DNA sequencing and genome assembly
Total DNA was extracted from young leaves with the DNeasy Plant Mini Kit (Qiagen, CA, USA). DNA was sheared by nebulization with compressed nitrogen gas, yielding fragments of 300 bp in length, and fragmentation quality was checked on a Bioanalyzer 2100 (Agilent Technologies). Paired-end libraries were prepared with the Mate Pair Library Preparation Kit (Illumina, San Diego, California, USA) in accordance with the manufacturer’s instructions. Genomic DNA was sequenced on a single lane with multiplexing on HiSeq2000 flow cell lanes (Illumina Inc.).
For each species, the raw reads were assembled into non-redundant contigs with Velvet1.2.07 [18], a de novo sequence assembly software package, with k = 30 and scaffolding contigs having a minimum length of 100 bp. All contigs were then mapped against the reference cp genome in Camellia sinensis [7] with BLAST (http://blast.ncbi.nlm.nih.gov/) similarity searches against the NCBI nr database by using the default search parameters. To identify the chloroplast contigs, all the returned contigs were blasted to the reference genomes. Primer walking and additional Sanger sequencing were then used to fill the gaps between the seven to twelve large contigs and to verify the junctions between the single-copy and the IRs regions (S1 Table).
Gene annotation
Initial gene annotation of the four chloroplast genomes was performed with Dual Organellar GenoMe Annotator (DOGMA; [19]). The tRNA genes were predicted with ARAGORN [20] and tRNAscan-SE [21]. The circular gene maps were drawn by the OrganellarGenomeDRAW tool (OGDRAW), followed by manual modification [22]. Comparison of Actinidia cp genome structures was performed by the mVISTA program in Shuffle- LAGAN mode [23] by using the annotation of Camellia sinensis as the reference.
Repeat structure
Size and location of both direct (forward) and inverted (palindromic) repeats in the Actinidia cp genome were determined by running REPuter [24] at a minimal repeat size ≥ 30 bp with a Hamming distance of 3.
Microsatellite (mono-, di-, tri-, tetra-, penta-, and hexanucleotide repeats) detection was performed by using MISA [25] with thresholds of nine repeat units for mononucleotide SSRs, five repeat units for di- and trinucleotide SSRs, and three repeat units for tetra-, penta- and hexanucleotide SSRs.
Phylogenetic analysis
We sampled fifteen species representing the asteroid lineage of angiosperm to reconstruct a phylogeny of asterids with cp genes (S2 Table). The 72 protein-coding genes shared by the chloroplast genomes of 15 asterid members (S2 Table) were used for phylogenetic analysis. Arabidopsis thaliana was used as the outgroup. The sequences were aligned with MUSCLE [26] with the default settings and concatenated into a single alignment of 55,370 characters. Optimal trees were inferred with maximum parsimony (MP) and Maximum likelihood (ML) as implemented in PAUP* version 4.0b10 [27]. For all analyses, characters were equally weighted, gap regions were excluded in the phylogenetic analyses, and multistate characters were treated as uncertainties. Prior to the ML analyses, the Akaike information criterion (AIC) was employed to determine the best model and parameters settings with the program Modeltest 3.07 [28]. Analyses were performed with the following options implemented: heuristic search mode used 1000 random-addition sequence replicates holding 20 trees at each step, tree bisection-reconnection (TBR) branch-swapping, MULTrees in effect, and steepest descent off. Bootstraps analyses were employed with heuristic searches and 1000 replicates. Because the results from ML analyses were congruent with the results of the MP analyses, they are not presented here.
Results and Discussion
Genome sequencing and assembly
Illumina paired-end (300 bp) sequencing produced 310.9, 252.8, 274.9 and 286.8 Mb of data for A. chinensis (2×), A. chinensis (4×), A. chinensis var deliciosa (4×) and A. chinensis var deliciosa (6×), respectively. The N50 of contigs ranged from 9898 bp to 22,416 bp. A total of twelve, eight, fifteen and seven contigs with lengths of 131,930, 131,859, 130,725 and 131,916 bp were found to be derived from cpDNAs for A. chinensis (2×), A. chinensis (4×), A. chinensis var deliciosa (4×) and A. chinensis var deliciosa (6×), respectively. Four junction regions between IRs and SSC/LSC in each cp genome were confirmed by PCR amplifications and Sanger sequencing. The sequences of four chloroplast genomes were deposited in GenBank (accession numbers KP297242 through KP297245).
Organization of chloroplast genome
The nucleotide sequences of the four cp genomes range from 156,346 bp in A. chinensis (2×) to 157,375 bp in A. chinensis var deliciosa (6×) (Table 1). All four cp genomes share the typical quadripartite cp structure, with a pair of inverted repeats (IRs 24,013–24,391 bp) each separated by a SSC (20,332–20,336 bp) and a LSC (87,984–88337 bp) (Table 1). This structure agrees well with that based on restriction mapping of [29], although the total lengths slightly differ.
Table 1. Summary of chloroplast genome characteristics in Actinidia.
| A. chinensis (2×) | A. chinensis (4×) | A. chinensis var deliciosa (4×) | A. chinensis var deliciosa (6×) | |
|---|---|---|---|---|
| Size (bp) | 156346 | 156810 | 156741 | 157375 |
| LSC length (bp) | 87984 | 88337 | 88267 | 88261 |
| SSC length (bp) | 20336 | 20333 | 20332 | 20332 |
| IR length (bp) | 24013 | 24070 | 24071 | 24391 |
| Number of genes* | 113 | 113 | 113 | 113 |
| Protein-coding genes* | 79 | 79 | 79 | 79 |
| tRNA genes* | 30 | 30 | 30 | 30 |
| rRNA genes | 4 | 4 | 4 | 4 |
| GC content (%) | 37.2 | 37.2 | 37.2 | 37.2 |
* numbers refer to the number of different genes
When duplicated genes are counted only once, the Actinidia cp genomes contain 113 unique genes (unique ORFs were not taken into account) including 79 protein-coding genes, 30 tRNA genes and four rRNA coding genes (Fig 1 and Table 1). Four protein coding, four rRNA and eight tRNA genes are duplicated and located in the IR regions. Fourteen of the protein-coding genes and eight of the tRNA genes contain introns, 16 of which contain a single intron, whereas one (ycf3) has two introns (Table 2). The gene rps12 is trans-spliced; the 5’ end exon is located in the LSC region and the 3’ exon and intron are duplicated and located in the IR regions. Gene content is typical for the plastomes of the dicotyledonous angiosperms, being most similar to that of Camellia sinensis (Theaceae, [7]) as compared with those land plants sequenced. Most protein-coding genes have the standard AUG as the initiator codon [3], but ndhD has an initiator codon of ACG. The trnfM-CAU genes are duplicated in the LSC of the Actinidia chloroplast genome and separated by 14 bp with the same orientation. tRNA gene duplications have also been reported for black pine [30] and the green algae [31]. The overall GC content of the Actinidia chloroplast genome is 37.2%. The GC content of the Actinidia cp genome is close to that of Ardisia polysticta (37.07%) and other asterids [6].
Fig 1. Gene maps of the Actinidia plastid genome.
Genes shown on the outside of the map are transcribed clockwise, while genes on the inside are transcribed counter-clockwise. Genes belonging to different functional groups are color-coded.
Table 2. List of genes encoded by the Actinidia chinensis plastome.
| Category | Group of gene | Name of gene |
|---|---|---|
| Photosynthesis | Photosystem I | psaA, psaB, psaC, psaI, psaJ, ycf3 a , ycf4 |
| Photosystem II | psbA, psbB, psbC, psbD, psbE, psbF, psbH, psbI, psbJ, psbK, psbL, psbM, psbN, psbT, psbZ | |
| NADH oxidoreductase | ndhA b , ndhB b , c , ndhC, ndhD, ndhE, ndhF, ndhG, ndhH, ndhI, ndhJ, ndhK | |
| Cytochrome b/f complex | petA, petB b , petD b , petG, petL, petN | |
| ATP synthase | atpA, atpB, atpE, atpF b , atpH, atpI | |
| Large subunit of rubisco | rbcL | |
| Self-replication | Large subunit ribosomal proteins | rpl2 b , rpl14, rpl16 b , rpl20, rpl22, rpl23, rpl32, rpl33, rpl36 |
| Small subunit ribosomal proteins | rps2, rps3, rps4, rps7 c , rps8, rps11, rps12 a , rps14, rps15, rps16 b , rps18, rps19 | |
| RNA polymerase subunits | rpoA, rpoB, rpoC1 b , rpoC2 | |
| Ribosomal RNAs | rrn16 c , rrn23 c , rrn4.5 c , rrn5 c | |
| Transfer RNAs | trnA-UGC b , c , trnC-GCA, trnD-GUC, trnE-UUC, trnF-GAA, trnG-GCC, trnG-UCC b , trnH-GUG c , trnI-CAU c , trnI-GAU b , c , trnK-UUU b , trnL-CAA c , trnL-UAA b , trnL-UAG, trnfM-CAU, trnM-CAU, trnN-GUU c , trnP-UGG, trnQ-UUG, trnR-ACG c , trnR-UCU, trnS-GCU, trnS-GGA, trnS-UGA, trnT-GGU, trnT-UGU, trnV-GAC c , trnV-UAC b , trnW-CCA, trnY-GUA | |
| Other genes | Translational initiation factor | infA |
| Maturase K | matK | |
| Envelope membrane protein | cemA | |
| Subunit of acetyl-CoA-carboxylase | accD | |
| c-type cytochrome synthesis gene | ccsA | |
| Proteins of unknown function | ycf1, ycf2 c | |
| Putative pseudogenes | ycf15 c |
aGene with two introns.
bGene with one intron.
cGenes located in the inverted repeats.
The overall sequence identity of the four Actinidia cp genomes was plotted with mVISTA with Camellia sinensis as a reference (Fig 2). The IRs show lower sequence divergence than that in the single-copy regions, possibly due to copy correction between IR sequences by gene conversion [32]. As expected, non-coding regions exhibit a higher divergence than coding regions, and the most divergent regions among the four cp genomes are localized in the intergenic spacers. Intergenic regions with high degrees of divergence included rps16-trnQ, petN-psbM, trnT-trnL, ndhD-ccsA, ndhI-ndhG, psbI-trnS, rrn5-ndhF, and trnH-psbA. Therefore, developing universal primers for these intergenic regions could aid in assessing phylogenetic relationships among Actinidia species.
Fig 2. Sequence identity plots between four sequenced chloroplast genomes, with Camellia sinensis as a reference.
The vertical scale indicates the identity percentage (50% to 100%). The horizontal axis corresponds to the coordinates within the chloroplast genome. Annotated genes are displayed along the top.
Repeat structure
Mononucleotide microsatellite length polymorphisms have been used as markers in cp genomes for understanding cp evolutionary history due to their high rates of variability [33]. In our MISA analyses, 65 SSRs with a length of at least 10 bp in the Actinidia plastid genomes were detected, of which 61 are mononucleotide repeats, two are dinucleotide repeats, and two are trinucleotide repeats. No pentanucleotides or hexanucleotides were found. Sixty homopolymer loci are composed of A/T repeats, whereas only one is composed of C repeats. All of the dinucleotides are composed of multiple copies of AT/TA repeats. SSR loci are mostly present in noncoding regions. Of the 65 loci, 27 were polymorphic (Table 3). Hence, the plastid genome sequences of Actinida will be useful in developing lineage-specific cpSSR markers, which are widely used in population-genetic and evolutionary studies of plant.
Table 3. Polymorphic microsatellites in the chloroplast genome of Actinidia.
| Unit | SSR type | Location |
|---|---|---|
| A | (A)n | trnK-rps16, rps16-trnQ, trnS-trnR, atpF intron, atpH-atpI, psbZ-trnG, ycf3-trnS, trnT-trnL, ycf4-cemA, petA-psbJ, psbE-petL |
| T | (T)n | rps16-trnQ, trnT-trnL, ndhC-trnV, accD-psaI, psaI-ycf4, rps8-rpl14, rpl16 intron |
REPuter [24] identified a total of 34 pairs of repeats (30 bp or longer) with a sequence identity greater than 90% in the Actinidia cp genome, of which 29 are forward and 5 are inverted repeats (Table 4). Searches for shorter and/or more divergent repeats would likely identify many additional repeated sequences. The repeats range from 30 to 79 bp in length, and are repeated from two to nine times. Most of the repeated sequences occur in regions of noncoding DNA, whereas some were found in protein-coding regions (e.g. ycf2). A substantial number of repeated sequences identified in chloroplast genomes, especially in intergenic spacer regions, have been reported in a number of angiosperm lineages, including other asterids (e.g. [7]).
Table 4. Repeated sequences in the Actinidia chloroplast genomes.
| No. | Size (bp) | Type | Repeat number | Location | Region |
|---|---|---|---|---|---|
| 1 | 79 | F | 2 | trnfM-CAU | LSC |
| 2 | 76 | F | 2 | IGS (rps12/psbT) | LSC |
| 3 | 76 | F | 2 | IGS (rps12/psbT) | LSC |
| 4 | 68 | F | 2 | IGS (rbcL/accD) | LSC |
| 5 | 57 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 6 | 56 | F | 2 | IGS (rps12/psbT) | LSC |
| 7 | 54 | F | 2 | IGS (rbcL/accD) | LSC |
| 8 | 49 | F | 3 | IGS (trnH-GUG/trnI-CAU) | IRa,b |
| 9 | 48 | P | 1 | CDS (rps18) | LSC |
| 10 | 47 | P | 1 | IGS (petB/petD) | LSC |
| 11 | 47 | F | 2 | IGS (rps12/psbT) | LSC |
| 12 | 44 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 13 | 42 | F | 4 | IGS (rps12/trnV-GAC), ndhA intron | IRa,b |
| 14 | 41 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 15 | 40 | F | 9 | IGS (trnN-GUU/ycf1) | IRa,b |
| 16 | 39 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 17 | 38 | F | 3 | IGS (rps15/trnN-GUU) | IRa,b |
| 18 | 37 | F | 2 | IGS (trnH-GUG/trnI-CAU) | IRa,b |
| 19 | 37 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 20 | 36 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 21 | 35 | F | 2 | CDS (ycf2) | IRa,b |
| 22 | 35 | F | 2 | IGS (trnN-GUU/ ycf15) | IRa,b |
| 23 | 34 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 24 | 34 | F | 2 | CDS (rps18) | LSC |
| 25 | 34 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 26 | 33 | F | 2 | CDS (ycf2) | IRa,b |
| 27 | 33 | P | 1 | IGS (accD/psaI) | LSC |
| 28 | 32 | F | 2 | IGS (trnH-GUG/trnI-CAU) | IRa,b |
| 29 | 32 | F | 2 | IGS(rrn4.5/rrn5), | IRa,b |
| 30 | 32 | F | 2 | IGS (rps15/trnN-GUU) | IRa,b |
| 31 | 31 | F | 2 | IGS (rps12/psbT) | LSC |
| 32 | 30 | F | 2 | CDS (ycf2) | IRa,b |
| 33 | 30 | P | 1 | trnS-GCU | LSC |
| 34 | 30 | P | 1 | CDS (rps18) | LSC |
F: Forward; P: Inverted; IGS: Intergenic spacer; CDS: protein-coding regions.
The availability of plastid genome sequences should provide valuable information for plastid genetic engineering [14,15]. Plastid transformation is based on homologous recombination between the vector and plastid genome sequences. Thus, knowledge of the nucleotide sequence of chloroplast genome would be helpful to identify the optimal intergenic spacers for transgene integration and to develop species-specific cp transformation vectors. In the present study, the direct or palindromic repeat sites found in the LSC region of the Actinidia cp genome represent potential site-specific recombination sites that could be used in the development of a kiwifruit-specific chloroplast vector.
ClpP lost in the Actinida cp genome
Gene loss and gene transfer to the nucleus is a common feature of cp genomes [34,35]. For instance, the rpl22 gene of Fagaceae [36] and Fabaceae [37], the infA in rosids [38], the rpl32 gene in Populus and Salicaceae [39,40], and accD in Trifolium [41] have been transferred to the nuclear genome. The clpP gene, which encodes the Proteolytic subunit of Clp-protease with over 200 amino acids, is widely distributed among the cp genome of various land plant species [42]. The clpP gene encoded in the Camellia sinensis chloroplast genome are absent in the Actinida cp genome [7]. The close relationship of these two plant families indicates that this difference reflects a relatively recent event, either gene loss or functional transfer to the nucleus.
Among the angiosperm plastids investigated thus far, clpP is also partially or completely missing from the plastid genome of Passiflora (Passifloraceae, [43]), Trachelium caeruleum (Fabaceae, [44]), Scaevola (Goodeniaceae) [42] (Wicke et al., 2011), and Vaccinium macrocarpon (Ericaceae, [8]). The availability of the sequenced A. chinese nuclear genome gave us opportunity to search for these missing genes by using the C. sinensis chloroplast-encoded proteins. Fourteen gene fragments encode the ATP-dependent clp-protease proteolytic subunit were annotated in the kiwifruit genome (http://bioinfo.bti.cornell.edu/cgi-bin/kiwi/home.cgi). In this study, two fragments (135 and 198 bp) from kiwifruit genome CDS sequences were found to have 77% and 89% similarity to clpP encoded in the cpDNA of C. sinensis, which suggests clpP has probably been replaced by a copy of the same gene that was transferred to the nucleus during chloroplast evolution, but this needs to be further explored.
IR contraction
The IR boundaries were compared among four families in the asterids, including Actinidia (Actinidiaceae), Vaccinium macrocarpon (Ericaceae) [8], Ardisia polysticta (Myrsinaceae), [6] and Camellia sinensis (Theaceae) [7]. The cpDNA of Actinidia is collinear with the previously published plastomes of Ardisia polysticta and Camellia sinensis in gene order and overall homology. Fig 3 shows the detailed comparison of the IR/single copy (SC) boundaries between four representative members of basal asterids (Camellia, Ardisia, Vaccinium, and Actinidia). In the angiosperms, the downstream sequences of IRb/SSC are conserved, with the ndhF gene adjacent to it. In the Actinidia, Camellia and Ardisia cp genomes, the IR expands into the ycf1 gene and inserts the ycf1 pseudogene at the IRb/SSC border, whereas ycf1 is lost in Vaccinium. For Camellia and Ardisia, the IRa/LSC junction is found within rps19 and pseudogenes of rps19 are located at the IRa/LSC boundary. However, in Actinidia the rps19 gene does not extend into the IR region, and thus the rps19 pseudogene is not observed. The IR extends into the psbA gene and inserts a short psbA pseudogene at the IRb/LSC border, which is similar to that of Vaccinium.
Fig 3. Comparison of the border positions of LSC, SSC, and IR regions in four basal asterid species.
Boxes above the main line represent the genes at the IR/SC borders. The pseudogenes at the borders are shown by ψ.
Compared to other species, the length of the IRs in the kiwifruit cp genome is fairly low; for example, in Theaceae, the size of the IR regions range from 26,025 bp to 26,057bp [7]; and in the basal asterids, such as Ericaceae, the length of the IRs are 34,232 bp [8]. The IR sequence in Actinidia is about 2 kb smaller than that in Ardisia cpDNA [6]. Hence, there has also been contraction of the IR in Actinidia at the IR/SSC boundary relative to the IRs in Camellia and Ardisia. However, size variation by contractions within IR sequences contributes little to overall size variation between cp genomes of different taxa in asterids.
Phylogenetic analysis
To gain an insight into the position of the Actinidia within the asterids, we generated data sets of 72 protein-coding genes from the completely sequenced chloroplast genomes of 15 asterids and one outgroup (S2 Table). The 72 genes contain 8,671 potentially parsimony-informative and 9,342 uninformative nucleotide characters. Parsimony analyses yielded a singe most-parsimonious tree (MPTs) with a length of 35,711, a consistency index of 0.66 and a retention index of 0.44 (Fig 4). The MP bootstrap tree resolved 16 nodes, of which 12 had strong bootstrap support (BS) of 99–100%, one had moderate support of 63%, and three had weak support at 5–30%. The results strongly support the position of the Actinidiaceae within Ericales, the basal position of Ericales within asterids, and the subdivision of euasterids into euasterids I (Gentianales, Lamiales, Solanales) and euasterids II (Apiales, Asterales). The phylogenetic trees in this study also indicates a close relationship between the Actinidiaceae and the Ericaceae, with high bootstrap support (100%). These results agree with data confirmed by phylogenetic methods based on 3 coding and 3 non-coding chloroplast DNA markers [45] and 78 orthologous chloroplast genes [6]. However, interrelationships among six families (Sarraceniaceae, Actinidiaceae, Roridulaceae, Clethraceae, Cyrillaceae, and Ericaceae) within the ericoid group based on these markers remain unresolved. The sequenced cp genomes provide large amounts of genetic information for improving resolution in phylogenetic studies. Thus, expanded taxon sampling will be required to acquire the accurate relationship in asterids.
Fig 4. Phylogenetic position of Actinidia as inferred by MP analyses of 72 protein-coding genes.
The MP tree has a length of 35,711, with a consistency index of 0.66 and a retention index of 0.44. Numbers above the lines indicate the maximum parsimony bootstrap value > 50% for each clade. The position of Actinidia is shown in boldface.
Conclusions
The complete chloroplast sequence of Actinidia of the basal asterid was obtained with Illumina sequencing technology and Sanger sequencing. This is the first chloroplast genome sequenced in the Actinidiaceae family. The chloroplast genome of Actinidia has a very similar size and organization to those of other sequenced angiosperms. However, IR contraction was observed in Actinidia by comparing its cp genome with those of others in the asterids. Furthermore, we found that the clpP gene was lost in the Actinidia chloroplast genomes and may have been transferred to the nucleus during chloroplast evolution. The abundant and variable cpSSR loci identified in Actinidia will be useful in characterizing the population genetics of Actinidia. The phylogenetic relationships yielded by a dataset of sequences of 72 shared protein-coding genes of Actinidia and 14 other asterids genomes strongly support the placement of Actinidiaceae in Ericales within the basal asterids. Our data presented in this paper should provide important information to facilitate plastid genetic engineering of kiwifruit. For instance, the complete DNA sequence of chloroplast genomes of Actinidia is helpful to identify the optimal intergenic spacers for transgene integration and to develop kiwifruit-specific chloroplast vector.
Supporting Information
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(DOCX)
Acknowledgments
We wish to thank Peter W. Fritsch and Lei Gao for their valuable comments on the manuscript. This work was partly supported by the Natural Scientific Foundation of China (31370251) and Fund of Science and Technology Service, Chinese Academy of Sciences (KFJ-EW-STS-076).
Data Availability
The sequences of four chloroplast genomes were deposited in GenBank (accession numbers KP297242 through KP297245).
Funding Statement
This work was partly supported by the Natural Scientific Foundation of China (31370251) and Fund of Science and Technology Service, Chinese Academy of Sciences (KFJ-EW-STS-076).
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Associated Data
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Supplementary Materials
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Data Availability Statement
The sequences of four chloroplast genomes were deposited in GenBank (accession numbers KP297242 through KP297245).