Skip to main content
Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2020 Jan 7;5(1):402–403. doi: 10.1080/23802359.2019.1704196

The complete plastid genome and phylogenetic analysis of Codium fragile

Xuli Jia a, Tao Liu a,b,, Ruoran Li b, Yuemei Jin a
PMCID: PMC7748513  PMID: 33366576

Abstract

Codium fragile, a nutrient-rich green algae that is both edible and medicinal, it is called a ‘rat tail’ because of its unique shape, it can reach up to a metre in length and has the functions of clearing heat and detoxifying, detumescence and water, and repelling insects. The plastid genome sequence of C. fragile is 83,422 bp. A total of 105 genes were determined, including 77 protein-encoding genes, 3 rRNA genes, and 25 tRNA genes. Phylogenetic analysis showed that C. fragile clustered together into a single branch with C. simulans and Codium sp. 'arenicola' as sister branches. The plastid genome analysis will help the understanding of Chlorophyta evolution.

Keywords: Codium fragile, plastid genome, phylogenetic analysis, Chlorophyta


Codium fragile is a popular, edible and medicinal green alga belonging to the family Codiaceae. It is widely distributed along the shores of East Asia, Oceania and Northern Europe (Chaiwat Monmai et al. 2019). It has also been used as an oriental medicine for the treatment of diseases, such as enterobiosis, dropsy, and dysuria (Lee et al. 2010). Codium fragile extracts have been demonstrated to possess thrombolytic, anticoagulant, antiplatelet (Choi et al. 2013), anti-inflammatory (Kang et al. 2012). However, genomic studies on this species are relatively limited. In this study, we sequenced, embeled and annotated the plastid DNA of C. fragile, conducted a systematic genome study to evaluate the evolutionary trend of plastid DNA, and studied the phylogenetic relationship between C. fragile and other green algae with red algae Gracilaria firma (NC_033877.1) served as the out-group.

The determination of the complete C. fragile plastid genome sequence by next-generation sequencing methods was conducted. The specimen was collected from China (Rongcheng, Shandong Province, 37°08′26.07″N, 122°26′45.39″E) and stored at the Culture Collection of Seaweed at the Ocean University of China (accession no. 2016070047). The total DNA was extracted using the modified CTAB method (Doyle and Doyle 1990). Paired-end reads (150 bp) were sequenced by using Illumina HiSeq system (Illumina, San Diego, CA). tRNAscan-SE Search Server (Schattner et al. 2005) were used to identified the tRNA genes. The other plastid genomic regions were annotated with Geneious R10 (Biomatters Ltd, Auckland, New Zealand), using the Codium sp. 'arenicola' (NC_037366.1) and C. simulans (NC_032043.1) plastid genome as reference sequences.

The complete C. fragile plastid genome is a circular DNA molecule measuring 83,422 bp in length with the overall G + C content of the complete plastid genome is 27.3% (GenBank accession no. MN733705). The plastid genome contains 105 genes, including 77 protein-coding genes, 3 rRNA genes (rnl rRNA, rns rRNA and rrn5 rRNA) and 25 tRNA genes. The nucleotide composition was 35.56% A, 12.93% C, 14.34% G, and 37.17% T. The length of the coding region was 70,700 bp, corresponding to 84.75% of the total length. Of the 77 protein-coding genes in C. fragile, 66 (85.71%) started with the initiation codon ATG and 11 (14.29%) started with the non-initiation codon ATG, 68 (88.31%) ended with the TAA stop codon, 4 (5.19%) with TAG (ycf12, cemA, chlB and psbZ) and 5 (6.49%) with TGA (chlL, atpI, rps2, rpl32 and ycf47).

Twenty-three shared plastid genome protein sequences from 17 green algae and 1 red algae including Codium fragile were used to conduct phylogenetic analysis by using MrBayes 3.1.2 software (Ronquist and Huelsenbeck 2003). Poorly aligned regions were removed by using the Gblocks server (Castresana 2000). According to their original class, Ulvophyceae clustered together into a single branch, Trebouxiophyceae and Chlorophyceae clustered together into another branch. Codium fragile showed a closer relationship with C. simulans and Codium sp. 'arenicola' in Ulvophyceae (Figure 1). This complete plastid genome analysis of C. fragile helps us better understand the evolutionary process of Chlorophyta.

Figure 1.

Figure 1.

Phylogenetic tree (Bayesian inference) based on complete plastid genomes of Chlorophyta. Support values for each node were calculated from Bayesian posterior probability (BPP). Asterisks following species names indicate newly determined plastid genomes.

Funding Statement

This work was supported by China-ASEAN Maritime Cooperation Fund.

Disclosure statement

No conflicts of interest for all the authors including the implementation of research experiments and writing this article were reported.

References

  1. Castresana J. 2000. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol Biol Evol. 17(4):540–552. [DOI] [PubMed] [Google Scholar]
  2. Monmai C, You S, Park WJ. 2019. Immune-enhancing effects of anionic macromolecules extracted from Codium fragile on cyclophosphamide-treated mice. PLoS One. 14(2):e0211570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Choi JH, Sapkota K, Park SE, Kim S, Kim SJ. 2013. Thrombolytic, anticoagulant and antiplatelet activities of codiase, a bi-functional fibrinolytic enzyme from Codium fragile. Biochimie. 95(6):1266–1277. [DOI] [PubMed] [Google Scholar]
  4. Doyle JJ, Doyle JL. 1990. Isolation of plant DNA from fresh tissue. Focus. 12:13–15. [Google Scholar]
  5. Kang CH, Choi YH, Park SY, Kim GY. 2012. Anti-inflammatory effects of methanol extract of Codium fragile in lipopolysaccharide-stimulated RAW264.7 cells. J Med Food. 15(1):44–50. [DOI] [PubMed] [Google Scholar]
  6. Lee JB, Ohta Y, Hayashi K, Hayashi T. 2010. Immunostimulating effects of a sulfated galactan from Codium fragile. Carbohydr Res. 345(10):1452–1454. [DOI] [PubMed] [Google Scholar]
  7. Ronquist F, Huelsenbeck JP. 2003. Mrbayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 19(12):1572–1574. [DOI] [PubMed] [Google Scholar]
  8. Schattner P, Brooks AN, Lowe TM. 2005. The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res. 33(Web Server issue):W686–W689. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Mitochondrial DNA. Part B, Resources are provided here courtesy of Taylor & Francis

RESOURCES