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Mitogenome Announcement

The complete mitochondrial genome of Pyropia pulchra (Bangiophyceae, Rhodophyta)

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Pages 3157-3158 | Received 09 Jul 2020, Accepted 11 Jul 2020, Published online: 12 Aug 2020

Abstract

Pyropia pulchra (Hollenberg) S.C. Lindstrom & Hughey is a foliose seaweed in Bangiales order distributed in North America. We assembled the complete mitochondrial genome sequence of Pyropia pulchra (33,190 bp), and annotated 26 protein-coding genes, 24 transfer RNAs, and 2 ribosomal RNAs. We analyzed a maximum likelihood tree using conserved 23 mitochondrial genes from Bangiales species. The mitochondrial phylogeny of Bangiales species shows a strong monophyletic relationship of genus Pyropia, and the taxonomic position of P. pulchra within the genus.

The red algal genus Pyropia J. Agardh belongs to Bangiales order (Bangiophyceae, Rhodophyta) that includes the valued marine aquaculture crop, worth over US $1 billion per year (Blouin et al. Citation2011; Kim et al. Citation2014). As the economic significance for cultivation, the cultivars are spread and mostly distributed in worldwide intertidal zones. The most Bangiales species are morphologically simple that are grouped into filamentous and foliose seaweeds, therefore there were many taxonomically cryptic species classified by molecular phylogenetic studies (Sutherland et al. Citation2011; Kucera and Saunders Citation2012; Harden et al. Citation2016; Koh and Kim Citation2018). Especially, diverse species were segregated from the previous larger and polyphyletic genus Porphyra (Milstein and de Oliveira Citation2005; Nelson et al. Citation2006; Blouin et al. Citation2011).

Pyropia pulchra (Hollenberg) S.C. Lindstrom & Hughey is one of the foliose Bangiales species mainly distributed in North America (British Columbia, California, Oregon; Kucera and Saunders Citation2012; Augytė and Shaughnessy Citation2014), and this species was discovered as a cryptic species from genus Porphyra based on molecular marker and plastid multigene phylogeny (Lee et al. Citation2016; Lindstrom and Hughey Citation2016). In the previous study, to construct the plastid genome of P. pulchra, the herbarium specimen of P. pulchra (UC1879714; the University of California at Berkeley, USA), collected at the type locality (Moss Beach, California, USA), was used for the genome sequencing, and they suggested a clear phylogenetic position of P. pulchra within the Bangiales (Lee et al. Citation2016). However, the phylogenetic position of P. pulchra using mitochondrial genome is still unknown.

To construct the mitochondrial genome of P. pulchra (UC1879714), we used the previously generated genome data of P. pulchra (Lee et al. Citation2016), and contigs of the mitochondrial genome were sorted by local BLAST search (e-value cutoff = 1.e–05). The consensus mitochondrial genome of P. pulchra (33,190 bp, GC = 30.7%; MT588076) was re-assembled from the sorted contigs, and confirmed by the read-mapping method using CLC Genomics Workbench (v5.5.1, CLC bio, Aarhus, Denmark). In the complete mitochondrial genome of P. pulchra, putative open-reading frames and conserved mitochondrial genes were manually predicted by BLASTx search (e-value cutoff = 1.e–05) with codon table 4 (The Mold, Protozoan, and Coelenterate Mitochondrial Code). Ribosomal RNAs (rRNAs) and transfer RNAs (tRNAs) were predicted by the RNAmmer 1.2 Server (Lagesen et al. Citation2007) and ARAGORN programs respectively (Laslett and Canback Citation2004). A total of 26 mitochondrial protein-coding genes, 24 tRNAs, and 2 rRNAs is annotated in the mitochondrial genome of P. pulchra (MT588076).

To construct the concatenated alignment of mitochondrial genes, conserved 23 protein-coding genes from 13 Bangiales and two outgroup species were used, and the genesets were aligned by MAFFT (v7.313; Katoh and Toh Citation2008) with default options. The Maximum Likelihood (ML) tree using the concatenated alignment was constructed by IQ-tree program (v1.6.12; Nguyen et al. Citation2015) with the options as follows: the gene partition information (-q), the model test (-m TEST), and ultrafast bootstrapping with 1000 replications (-bb 1000). The phylogenetic analysis shows a strong monophyletic relationship of genus Pyropia with high bootstrap supports (). In the ML tree, Pyropia nitida, P. endiviforlia, and P. kanakaensis are monophyly with P. pulchra (bootstrap support 100%), and this clade is clustered with the clade of P. perforata and P. haitanensis (bootstrap support 100%). The clade of P. tenera, P. yezoensis, and P. fucicola is located as a basal within the genus Pyropia (). There are relatively low bootstrap supports in the clades of genus Wildemania and Bangia (bootstrap support 50–56%; ). In addition, the clade of genus Porphyra in the mitochondrial phylogeny is located as basal within the Bangiales species () but in the plastid multigene phylogeny of Bangiales species, a clade of Wildemania schizophylla is located as a basal (Cao et al. Citation2018). To analyze a clear phylogenetic relationship of all genera within Bangiales, further study is required based on more mitochondrial genome data from the genera.

Figure 1. Maximum likelihood (ML) tree using 23 concatenated mitochondrial proteins from thirteen Bangiales and two florideophycean (outgroup) species.

Figure 1. Maximum likelihood (ML) tree using 23 concatenated mitochondrial proteins from thirteen Bangiales and two florideophycean (outgroup) species.

Acknowledgements

We thank Kathy Ann Miller (Herbarium, UC at Berkeley, USA) to provide the herbarium sample, and a special support from Hwan Su Yoon (Sungkyunkwan University, Suwon, Korea).

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The data that support the findings of this study are openly available in GenBank at https://www.ncbi.nlm.nih.gov/genbank/, reference number “MT588076”.

Additional information

Funding

This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) [2020R1C1C1010193].

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