Complete mitochondrial genome of Iksookimia hugowolfeldi and its phylogenetic position within genus Iksookimia

Abstract In this study, the complete mitochondrial genome sequences of Iksookimia hugowolfeldi, Korean loach species, was determined using next-generation sequencing analysis. The complete mitogenome of I. hugowolfeldi has 16,634 bp in length and consists of 13 protein-coding genes (PCGs), 22 tRNAs, two rRNAs, and one control region (D-loop). Both gene orders and characteristics were exactly accord with mitochondrial genome of other species those belong to the family Cobitidae. Phylogenetic analysis revealed that the establishment of taxonomic relationship between Iksookimia and Cobitis has still uncompleted because of the not distinguished as monophyletic status.

Genus Iksookimia belonging to family Cobitidae of order Cypriniformes has reclassified from Cobitis (Nalbant 1993). Iksookimia hugowolfeldi is one of the Iksookimia and known to as a Korean indigenous species (Kim 2009). This species has been confused with I. longicorpa because of similar morphological characteristics. However, in 1993, Nalbant T.T. found Yeongsan river-dwelling I. longicorpa group has several differences in morphological features and reported them as a new species named I. hugowolfeldi. Since the genus Iksookimia newly erected, the molecular studies have not conducted yet, whereas many studies have done in entire Cobitidae (Kim et al. 2000;Slechtov a et al. 2008;Kwan 2015). Therefore, we provide the complete I. hugowolfeldi mitogenome sequences (MN756662) for contributing the establishment of evolutionary relationship of Iksookimia.
The specimen was collected in Suncheon, Korea (35 01 0 20.04 00 N, 127 20 0 43.03 00 E) on 19 August 2019 and identified based on the morphological studies (Kim 1997(Kim , 2009). Voucher specimens (NSMK-FI00003) and mitochondrial DNA (mt-DNA) sample (NSMK-DN00003) were deposited in storage and freezer (-80 C) of Natural History Laboratory, National Science Museum (Daejeon, Korea), respectively. First, we isolated the mitochondria from caudal fin using Qproteome V R Mitochondria Isolation Kit (QIAGEN, Hilden, Germany). Then, we extracted DNA using DNeasy Blood & Tissue DNA isolation kit (QIAGEN). PCR product for next-generation sequencing (NGS) analysis was prepared using mitochondrial DNA by REPLI-g Mitochondrial DNA Kit (Qiagen). A genomic library was constructed using QIAseq FX single cell DNA library kit (QIAGEN) and used for NGS analysis in GnC Bio Co. (Daejeon, South Korea) followed by the Illumina Hi-Seq 2500 platform (San Diego, CA, USA).
The dataset for molecular phylogenetic analysis included 13 PCGs of five Iksookimia species. One relative species, Misgurnus mizolepis (MF579258) belonging to family Cobitidae, was used as outgroup. The maximum-likelihood analysis was conducted using PhyML 3.1 with GTR þ G model (Guindon et al. 2010). The bootstrap assembling was performed 1000 replication with rapid options.
In phylogenetic analysis, I. hugowolfeldi formed monophyletic clade. However, Cobitis and Iksookimia species were grouped with the state of undistinguished each genus (Figure 1). This result showed two genera have confusion in classification by the discordance between molecular relationship and morphological taxonomic status. Therefore, we suggested the taxonomical relationship between Iksookimia and Cobitis should be reestablished. Furthermore, we carefully supposed the consideration of Iksookimia as a synonym for Cobitis is necessary.

Disclosure statement
No potential conflict of interest was reported by the authors.