Abstract
Okenia is a speciose genus of the family Goniodorididae with more than 50 valid species. The phylogenetic relationships within the genus are little known. The mitogenome is a good marker to understand the phylogenetic relationships of relative species. This study was performed to sequence the mitogenome of O. hiroi. The mitogenome of O. hiroi was 14,583 bp in size and was composed of 37 genes, including 13 protein-coding genes, two ribosomal RNA genes, and 22 tRNA genes. The nucleotide composition was 30.5% A, 13.6% C, 16.5% G, and 39.4% T. The phylogenetic analysis showed that O. hiroi is sister to Notodoris gardineri (Aegiridae). This study recorded the first mitochondrial genome sequence of the family Goniodorididae.
Keywords: Okenia, mitogenome, nucleotide composition, phylogeny
The genus Okenia is composed of small to medium-sized nudibranchs (Pola et al. 2019). Because of its diversity, many new species of the genus Okenia have been recently described (Gosliner 2004; Pola et al. 2019). Currently, the genus includes more than 50 valid species that are distributed from the Pacific Ocean to the north and south Atlantic Ocean (Pola et al. 2019; Horton et al. 2021). In addition, there are limited studies on the phylogeny of the genus (Pola et al. 2019). Okenia hiroi is a species of the genus Okenia. This species was described from Japan and reported from Korea and Hong Kong (Jung et al. 2014). The analyses of the mitogenome genes of O. hiroi might be useful for understanding molecular identification and phylogeny of the genus. Therefore, this study aims at sequencing and analyzing structure of the mitogenome of O. hiroi.
The specimen of O. hiroi was collected from Munamjin-ri, Korea (38°18′14.75′′N, 128°34′1.05) in June 2020. Following the collection, the specimen (voucher number: SMU00087) was preserved in absolute ethanol and deposited at the Department of Biotechnology, Sangmyung University, Korea. Total DNA was extracted from the foot of the specimen. The extracted DNA was checked for puriyand concentration using a MaestroNano spectrophotometer (Maestrogen, Hsinchu, Taiwan). After library preparation, mitogenome sequencing was performed with MGISEQ-2000 (MGI, Shenzhen, China). MITObim (Hahn et al. 2013) was used for sequence assembly and MITOS (Bernt et al. 2013) was used for sequence annotation. Mitogenome sequences representing different families of the suborder Doridina and two species of the suborder Cladobranchia available in GenBank were obtained for phylogenetic analysis. All 37 genes of the mitogenomes were used for tree reconstruction. The partition schemes and best-fit model were searched in PartitionFinder 2 (Lanfear et al. 2017). MrBayes version 3.2.7a was applied to investigate the phylogenetic position of O. hiroi (Ronquist et al. 2012). For analysis, 10,000,000 generations were run and sampling was conducted every 1,000 generations.
The mitogenome of O. hiroi (GeneBank accession number: MW408699) was 14,583 bp long and contained 13 protein-coding genes, two rRNA genes, 22 tRNA genes. The nucleotide composition of the mitogenome was 30.5% A, 13.6% C, 16.5% G, and 39.4% T, with an A + T content of 69.9%. The size of 13 PCGs ranged from 156 bp (atp8) to 1,623 bp (nd5). Of 13 PCGs, there were nine genes (cox1, cox2, cytb, nad1, nd2, nad4, nad4l, nd5, and nd6) encoded on the H-strand and four remaining genes (atp6, atp8, cox3, and nd3) encoded on the L-strand. The mitogenome contained two rRNA genes with the size of 747 bp and 1,103 for 12S rRNA and 16S rRNA, respectively. Of the 22 tRNA genes, tRNA-Ser was the shortest gene (58 bp) and tRNA-Asn and tRNA-Asp were the longest genes (69 bp).
There were 27 intergenic regions in the mitogenome of O. hiroi, ranging from 1 to 108 bp. The longest intergenic region (108 bp) was located between cox1 and tRNA-Val genes. Compared to the other available mitogenomes of nudibranchs, this is the longest intergenic region between cox1 and tRNA-Val genes so far recorded. Also, there were five overlapping regions in the mitogenome of O. hiroi. The longest overlapping region (20 bp) was located over nd1 and nd5 genes.
Figure 1 shows the phylogenetic position of O. hiroi in the suborder Doridina. As seen from Figure 1, all species of Doridina were clustered together. The phylogenetic tree indicated that O. hiroi formed a clade with Notodoris gardineri (Aegiridae). In term of systematics, both Goniodorididae and Aegiridae belong to the super family Onchidoridoidea (Bouchet et al. 2017). Previous study also revealed a close relationship between Goniodorididae and Aegiridae (Hallas et al. 2017). In the future study, additional mitogenomes of the family Goniodorididae should be generated to investigate the relationships within the family.
Figure 1.
Phylogenetic position of Okenia hiroi in the suborder Doridina. GenBank accession numbers are put next to the species names. Two species from the suborder Cladobranchia (Hermissenda emurai and Protaeolidiella atra) are used as the outgroup. Posterior probability values are shown at the nodes.
Funding Statement
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea Government (MSIP) [No. NRF-2018R1D1A1B07042858].
Disclosure statement
No potential conflict of interest was reported by the authors.
Data availability statement
The genome sequence data that support the findings of this study is openly available in GenBank of NCBI at (https://www.ncbi.nlm.nih.gov/) under the accession no. MW408699. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA693411, SRR13555242, and SAMN17386532, respectively.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The genome sequence data that support the findings of this study is openly available in GenBank of NCBI at (https://www.ncbi.nlm.nih.gov/) under the accession no. MW408699. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA693411, SRR13555242, and SAMN17386532, respectively.

