Figures
Abstract
Costaria costata is a commercially and industrially important brown alga. In this study, we used next-generation sequencing to determine the complete plastid genome of C. costata. The genome consists of a 129,947 bp circular DNA molecule with an A+T content of 69.13% encoding a standard set of six ribosomal RNA genes, 27 transfer RNA genes, and 137 protein-coding genes with two conserved open reading frames (ORFs). The overall genome structure of C. costata is nearly the same as those of Saccharina japonica and Undaria pinnatifida. The plastid genomes of these three algal species retain a strong conservation of the GTG start codon while infrequently using TGA as a stop codon. In this regard, they differ substantially from the plastid genomes of Ectocarpus siliculosus and Fucus vesiculosus. Analysis of the nucleic acid substitution rates of the Laminariales plastid genes revealed that the petF gene has the highest substitution rate and the petN gene contains no substitution over its complete length. The variation in plastid genes between C. costata and S. japonica is lower than that between C. costata and U. pinnatifida as well as that between U. pinnatifida and S. japonica. Phylogenetic analyses demonstrated that C. costata and U. pinnatifida have a closer genetic relationship. We also identified two gene length mutations caused by the insertion or deletion of repeated sequences, which suggest a mechanism of gene length mutation that may be one of the key explanations for the genetic variation in plastid genomes.
Citation: Zhang L, Wang X, Liu T, Wang H, Wang G, Chi S, et al. (2015) Complete Plastid Genome of the Brown Alga Costaria costata (Laminariales, Phaeophyceae). PLoS ONE 10(10): e0140144. https://doi.org/10.1371/journal.pone.0140144
Editor: Hector Escriva, Laboratoire Arago, FRANCE
Received: June 9, 2015; Accepted: September 21, 2015; Published: October 7, 2015
Copyright: © 2015 Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All plastid sequences files are available from the NCBI GenBank database (accession number KR336545).
Funding: This work was supported by the Special Fund for Agro-scientific Research in the Public Interest (Grant No. 201203063), Project of Shandong Province Science and Technology Development Program (Grant No. 2014GGE29091) and the Fundamental Research Funds for the Central Universities (Grant No. 201362040).
Competing interests: The authors have declared that no competing interests exist.
Introduction
Costaria costata is an annual marine alga that belongs to the class Phaeophyceae, order Laminariales, and family Costariaceae. It grows naturally along the northern coast of the Pacific Ocean. In Asia, it is mainly distributed in the coastal waters of Japan and the Korean Peninsula [1], and has been newly cultivated in Korea [2]. C. costata propagates rapidly and therefore plays a central role in the restoration of marine pastures and construction of sea forests. In addition to its dietary value for marine animals such as abalone and sea urchins, C. costata is also important for the seaweed industry because it is used in the extraction of alginate, mannitol, and seaweed starch [3, 4]. C. costata is not distributed in China. However, because it has significant economic value and can potentially be cultivated, it was introduced in China in 1992. Sinc then, experiments have been carried out to optimize indoor cultivation [5]. In 2007, C. costata was successfully reproduced and bred in the sea areas of Dalian in the Liaoning Province. Currently, small-scale farming of C. costata is carried out in the sea areas of both Dalian and Rongcheng in North China.
The study of C. costata gradually intensified in recent years, mainly because this alga contains unique and abundant biologically active substances and sulfated fucan [6]. Previous research has shown that its dietary fiber has significant hypolipidemic effects [7]. However, with the exception of species taxonomy, population structure analysis, and its mitochondrial genome [8–11], little information about the molecular biology of C. costata has become available to date. Prior research has been restricted mainly to methods that use normal molecular markers, such as restriction fragment length polymorphism and small-subunit ribosomal DNA.
Plastids are important photosynthetic organelles with their own genomes. Plastid DNA is compact and has a fast evolutionary rate, which make it an ideal tool for evolutionary and population studies. The rbcL, matK, and psbA plastid genes are good taxonomic barcodes that are often used for species identification [12]. In recent years, determination of the evolution rates of plastid genomes has become an active area of research [13]. Rates of nucleotide substitution provide appropriate windows of resolution for the study of plant phylogeny at deep evolutionary levels. A description of the molecular change based on the complete plastid genome is essential for a full understanding of the mechanisms of mutation and evolutionary change [14]. Plastids arose through a process of primary and secondary endosymbiosis [15]; thus, unraveling their origin and evolution has been a challenging scientific puzzle. Phylogenetic analysis at the whole plastid genome level provides a more comprehensive and accurate mean to clarify the evolution of plastids.
We determined the complete plastid genome sequence of the large brown alga C. costata with next-generation sequencing. The sequence represents the first fully characterized plastid genome from the newly identified family of Costariaceae. In addition, we explored the evolutionary position of this alga based on the plastid genomic data currently available for other algae and higher plants. Saccharina japonica and Undaria pinnatifida have been main cultivated large brown seaweeds in China for decades. C. costata has great potential to follow these species in large-scale farming. All three algae belong to the order Laminariales. The present study not only contributes to efforts to exploit the advantageous characteristics of brown algae but also provides a scientific basis for the development of new algal breeds and further exploration of new marine sugar resources.
Materials and Methods
DNA Extraction
Algal material was provided by the Culture Collection of Seaweed at Ocean University of China in Qingdao (sample number: 2012050110). Gametophytes of C. costata were cultivated at 8–12°C in sterilized filtered seawater under fluorescent light (3000 lux; 12 h light/dark cycles). The gametophytes were concentrated on filter paper and subsequently washed three times with sterilized filtered seawater. Total DNA was extracted from fresh drained material according to a modified cetyltrimethylammonium bromide method [16].
Genome Sequencing and Assembly
Approximately 5 μg of purified DNA was used for the construction of short-insert libraries following the manufacturer’s protocol (Illumina Inc., San Diego, CA, USA). The sequenced libraries included short pair-end libraries with insert lengths of 250 bp, 300 bp, and 500 bp. Library construction and sequencing were performed by the Beijing Genomics Institute (Shenzhen, China).
The raw sequence reads corresponding to the plastid DNA were detected based on their similarity to the plastid genomes of U. pinnatifida, S. japonica, Ectocarpus siliculosus, and Fucus vesiculosus by using the Basic Local Alignment Search Tool (BLAST) software [17, 18]. For the short insert libraries, a total of 2,096,479 raw reads corresponding to plastid DNA were obtained with an average read length of 101 bp. The raw data provided approximately 1600-fold coverage of the plastid genome. Subsequently, these plastid-related reads were assembled by using SOAPdenovo software [19] with default assembly parameters (SOAPdenovo all -s assembly.conf -o mysample -K 49 -p 8 &). All the assembled contigs were aligned and ordered with respect to the reference plastid genomes using MEGA 6.0 software [20]. The sequence of the circular genome was completed via manual assembly. Polymerase chain reaction amplification and Sanger sequencing with the primers listed in S1 Table were performed to fill in the gaps and confirm the four junction regions.
Annotation and Analyses
Protein-coding genes and open reading frames (ORFs) were identified with BLASTN and BLASTX searches of the National Center for Biotechnology Information database [21]. The ribosomal RNA (rRNA) genes were identified via sequence alignment with known plastid genes of S. japonica and U. pinnatifida. The transfer RNA (tRNA) genes were identified by using tRNAscan-SE1.21 software [22]. The physical map of the circular genome was drawn with OGDRAW software [23]. Sequence alignment was performed and base composition determined by using BioEdit software. Gene substitution rates were calculated with MEGA 6.0 software [20]. Co-linear analyses of the five plastid genomes were conducted with Geneious software (version R7 7.0.6) [24].
Phylogenetic Analysis
Phylogenetic analysis was performed with plastid genomes from 43 taxa, including green algae, red algae, and brown algae, as well as two land plants. Cyanophora paradoxa was assigned as an outgroup. A list of 22 shared plastid genes were used for phylogenetic analysis (atpA, atpB, atpH, rbcL, petB, petG, psaA, psaB, psaC, psbA, psbB, psbC, psbD, psbE, psbF, psbL, psbN, rpl20, rps11, rps12, rps14, and rps19). Sequences were aligned with MEGA 6.0 software and edited manually. MrBayes v3.1.2 software [25] was used to investigate the evolutionary relationships based on 6,104 amino acids corresponding to the 22-protein dataset. Bayesian inference analysis was performed with two separate sequence analyses for four Markov chains (using default heating values), which were run for 500,000 generations, discarding the first 25% as burn-in [26]. The remaining trees were used to build a 50% majority rule consensus tree, accompanied by posterior probability values. FigTree v1.3.1 (http://tree.bio.ed.ac.uk/) was used to generate the phylogenetic trees.
Results and Discussion
Genome Organization and Comparison
The plastid DNA of C. costata is a 129,947 bp circular molecule. It contains a large single-copy (76,507 bp) and a small single-copy (42,622 bp) region separated by two inverted repeats (IRa and IRb: 5,409 bp), as shown in Fig 1. The overall A+T content is 69.13%, which is the second-lowest among the published Phaeophyceae plastid genomes to date (Table 1). The C. costata plastid genome contains 139 protein-coding genes including two ORFs, 27 tRNA genes, and six ribosomal RNA genes. None of the genes contains introns. The gene content and order are almost identical to those of the plastid genomes of S. japonica and U. pinnatifida; however, C. costata encodes fewer tRNAs. Similar to other reported species, the plastid genome of C. costata is compact, with an intergenic region that accounts for approximately 17.31% of the entire genome. Four pairs of genes overlap over 4 to 13 nucleotides.
Genes on the outside of the map are transcribed counterclockwise and those inside the map are transcribed clockwise. The innermost ring in gray represent the GC content.
In a comparison of the five known brown algal plastid genomes from Phaeophyceae, co-linear analysis showed that the protein-coding gene content and order in all three species from the Laminariales order are virtually identical (S1 Fig). All three have inverted repeats (IR) regions of similar length. Comparisons of plastid genome structures at the order level found significant differences between Laminariales, Fucales, and Ectocarpales but no apparent pattern in the overall genome structure. However, two long and conservative gene clusters with lengths of 30.7 Kb and 34.9 Kb containing 49 and 37 genes, respectively, were found among the five plastid genomes analyzed. In these gene clusters, the gene order of all five species is exactly the same, which demonstrates a conserved co-linear relationship between brown algal plastid genomes.
Codon Usage
The plastid genome of C. costata has three types of start codons. Whereas ATG is used for nearly all of the plastid genes, rps8 and psbF have GTG as the start codon. Remarkably, the same is true for U. pinnatifida and S. japonica (Table 2). In addition, ATT is the start codon for the atpA gene in C. costata and U. pinnatifida but not that in S. japonica. Three typical stop codons (TAA, TAG, and TGA) are found in the plastid genes of C. costata with preferences of 82.73% for TAA and 14.39% for TAG. The TGA stop codon is used only in the ycf24 gene, which also has a TGA stop codon in S. japonica and U. pinnatifida. The ycf40 gene in the U. pinnatifida plastid genome, also has a TGA stop codon.
ATG is the most commonly used translation initiation codon in all species studied thus far. Besides ATG, GTG serves as initiation codon in some bacterial and several red algal plastid genes [27]. Several examples exist in which the ATG start codon has mutated to ATT, which in turn stabilizes the binding of the initiator tRNAMet to the ribosome [28]. The plastid genomes of E. siliculosus and F. vesiculosus contain three and two genes, respectively, that have GTG start codon. In the five plastid genomes from Phaeophyceae, GTG start codon usage is concentrated in four genes (rpl3, rps8, rbcR, and psbF). The three plastid genomes from the same order of Laminariales show the same pattern of GTG start codon usage (see Table 2). Thus, the use of GTG as a start codon in these genes is strongly conserved.
TAG is the second most commonly used stop codon, after TAA. The frequency of the TAG stop codon in the plastid genes of five species from Phaeophyceae is 9.46–17.27%. As reported previously, in some cases, especially in the mitochondrial genome, TGA encodes tryptophan instead of a stop codon [29]. In plastid genes, however, TGA is a normal stop codon, and in E. siliculosus and F. vesiculosus we identified five and nine genes, respectively, with TGA stop codons. By contrast, in the three species of Laminariales, only one or two genes have TGA stop codons (ycf24, ycf40). Thus, Laminariales species use few TGA stop codons, differing substantially from E. siliculosus and F. vesiculosus plastid genomes. Based on the differences in the start and stop codons in plastid genes, as well as the evolutionary relationships between the five species from Phaeophyceae, we inferred a possible evolutionary pattern for their plastid genes (Fig 2).
Red boxes above the line represent the genes and their start codons; blue boxes below the line represent the genes and their stop codons.
Gene Substitution Rates
We calculated and compared the gene substitution rates of all the three plastid genomes of Laminariales, and the results demonstrated that the nucleotide substitution rates of all 137 protein-coding genes ranges from 0 to 20.88% with an overall substitution rate of 9.55%. The petF gene has the highest substitution rate (20.88%), and the petN gene has the lowest substitution rate (0; S2 Table). Analysis of the amino acid substitution rates showed an overall substitution rate of 5.57% for all genes, which is lower than the rates at the nucleotide level and indicates a certain proportion of synonymous substitutions. The overall comparison between different Laminariales species showed that plastid gene variation between C. costata and S. japonica is lower than that between each of those species and U. pinnatifida. The results showed that C. costata and S. japonica have a closer relationship, which differs from the results of the phylogenetic relationship analysis.
The mitochondrial genomes of the three Laminariales species C. costata, S. japonica, and U. pinnatifida have been published [30–32]. Therefore, we also calculated and analyzed the gene substitution rates among them. The results showed that the mitochondrial gene substitution rates ranges from 7.46% to 28.20% at the nucleotide level. The rps11 gene has the highest substitution rate and the atp9 gene has the lowest substitution rate (S3 Table). The overall comparative analysis of the three mitochondrial genomes indicated that the lowest interspecies substitution rates is between S. japonica and C. costata, which is in line with the results of the plastid gene analysis. Analyses of both plastid and mitochondrial genes support a closer phylogenetic relationship between S. japonica and C. costata than between each of these species and U. pinnatifida. Despite the plastid genome having a conservative rate of evolution and stable gene content, comparative molecular analyses revealed complex patterns of mutational change. Previous research found the silent site substitution rate of the mitochondrion to be lower than those of the plastid and nucleus in land plants [33]. However, recent organelle genome analyses from lineages outside of land plants suggest the opposite, that the substitution rate of plastids is lower than that of their mitochondria [13]. The three species used in our research belong to Laminariales and are related close enough for substitution rate analyses. Our results support that the plastid substitution rate is lower than that of the mitochondrion in algae groups with primary or secondary plastids.
Gene Length Change
The results of a comparison of the genetic differences between three Laminariales plastid genomes demonstrated differences in ycf35 and rpoA gene length between species. These gene length differences are caused by simple sequence repeats or deletions. The rpoA gene in the C. costata plastid genome is 6 bp longer than those in S. japonica and U. pinnatifida owing to a GAAAAA simple sequence repeat. However, neither the ORF nor the overall structure of the gene was affected by this 6 bp duplication. It may have formed during the process of gene replication, and we can infer that the duplication occurred after the differentiation of the families Costariaceae and Alariaceae. For the ycf35 gene, an insertion or deletion of a simple sequence of ATT or AAT makes its gene length 3 bp shorter in U. pinnatifida than those in S. japonica and C. costata (Fig 3). Neither the 3-bp nor the 6-bp length change influences the corresponding gene frame, but the mutations result in differences in both gene length and sequence.
The lines correspond to the amino acid triplet codon of each gene for three species, and the dash (–) represents the deletion of a base.
Simple sequence repeats, also called microsatellites, are an important source of gene recombination and variation [34]. In this study, we identified two gene length changes caused by insertion or deletion of a 3-bp or 6-bp repeat sequence in two plastid genes. These changes do not alter the original gene reading frame. Previous studies have shown that duplication or deletion of short repeated sequences are usually generated during the genome replication process, which cause gene length mutation [35]. All results and analyses of gene length changes in this study were verified and validated by polymerase chain reaction amplification and Sanger sequencing. Our results revealed a mechanism of gene length mutation that may be one of the most important sources of genetic variation in the plastid genome.
Phylogenetic Analyses
The phylogenetic tree with posterior probabilities based on 22 plastid protein-coding genes is presented in Fig 4. All taxa are clearly separated into two groups; one group consists of the green algae, Charophyta and land plants and represents the green plastid lineage branch. The other group represents the red plastid lineage that includes Porphyridium purpureum (emerging at the base of this branch), as well as red plastids and red-derived plastids. The red-derived plastid subgroup includes Haptophyta, Cryptophyta, and Heterokontophyta. Among the sub-branches of five brown algae belonging to the class Phaeophyceae, F. vesiculosus is the most isolated branch, followed by E. siliculosus. All three species from the order Laminariales form a clade, in which C. costata and U. pinnatifida receive a relatively high posterior probability that support a close relationship and are further grouped with S. japonica. This result does not correspond to the results of the gene substitution rates analysis performed in this study, and this inconsistency may be caused by the use of different data including only 22 protein-coding genes. In summary, all of our phylogenetic analyses support the conclusion that “primary” plastids are of both red and green lineage [36]. Nevertheless, in the red plastid lineage, P. purpureum was designated the most isolated branch and shows only a limited genetic relationship with other species. Considering that this plastid is a unicellular marine red alga and its gene order differs from that of other Rhodophyta, P. purpureum may represent a novel evolutionary plastid group [37].
In China, S. japonica and U. pinnatifida are currently the most important cultivated brown seaweeds farmed on a large scale. However, the use of single aquaculture species has seriously limited the development of the Chinese seaweed industry. Decades of simple and single breeding methods have gradually reduced the biodiversity of coastal aquaculture waters, and it is challenging to use cultivated seaweeds in the restoration of coastal ecosystems. C. costata is mainly distributed in the colder waters of the North Pacific, and normally grows attached to rocks. According to the results of this study, C. costata is closely related to S. japonica and U. pinnatifida phylogenetically. Therefore, it is almost impossible for C. costata to grow wildly in the temperate waters in China or damage the oceanic ecological balance and marine environment. Similar to S. japonica when first introduced in China, C. costata is a new type of large brown seaweed that has now been proven to be able to grow and reproduce in Dalian sea areas. It is urgent to accelerate the scientific study of the breeding and large-scale farming of this new species, which will be of great importance in the further development of the seaweed industry in China.
Supporting Information
S1 Fig. Comparison of five large brown algal plastid genomes from Phaeophyceae with Geneious software.
The shadow indicates the two conserved gene clusters.
https://doi.org/10.1371/journal.pone.0140144.s001
(TIF)
S1 Table. Sequences of the primers designed for gap filling and assembly validation.
https://doi.org/10.1371/journal.pone.0140144.s002
(PDF)
S2 Table. Substitution rates of 137 shared protein-coding genes among three plastid genomes from Laminariales.
https://doi.org/10.1371/journal.pone.0140144.s003
(PDF)
S3 Table. Substitution rates of 35 shared protein-coding genes among three mitochondrial genomes from Laminariales.
https://doi.org/10.1371/journal.pone.0140144.s004
(PDF)
Author Contributions
Conceived and designed the experiments: TL LZ. Performed the experiments: LZ. Analyzed the data: LZ XMW HYW. Contributed reagents/materials/analysis tools: HYW GLW SC CL. Wrote the paper: LZ.
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