Notoacmea concinna (NC) is, belonging to class Gastroda, family Acmaeidae, widely distributed along the coasts of the southern sea and Jeju Island in the Korea under the natural ecosystem. They mainly dwell in the rocky areas of the tidal zone. They have dense radial ribs and triangular pyramid of shell in shape. This shellfish eat sessile diatoms and microscopic algae.
Sulculus diversicolor supertexta (SDS) is, belonging to class Gastroda, family Haliotidae, widely distributed along the coasts of Jeju Island of Korea and the several sea areas in Japan. They mainly inhabit in the rocky shores of the low tidal zone to approximately 15 m in depth. This shell fish are reddish-brown in shell color with ridges and growth rings on shell surface. They also have green-brown stripes on dorsal surface of soft body and greenish-purple on pedal sole. They have 7–9 respiratory pores with flowing water in contrast to other abalones. Their larvae eat sessile diatoms, microscopic algae and some debris (Min, 2001).
Haliotis discus hannai (HDH) is, belonging to class Gastroda, family Haliotidae, widely distributed along the coasts of the Yellow Sea, southern sea and Jeju Island in the Korean Peninsula and the several sea areas in China and Japan under the natural ecosystem. Abalone mainly dwells in the rocky shores of the open sea with brown algae from the low tidal zone to approximately 20 m in depth. This shell fish are reddish-brown in shell color with ridges and growth rings on shell surface. They have also black and yellow stripes on dorsal surface of soft body and greenish-purple on pedal sole. Their sexual maturity is determined by the olive-green coloration of the ovary, and ivory-white of the testis. Adult abalone can eat green algae, Enteromorpha spp. and Ulva spp., brown algae, Undaria pinnatifida, Laminaria spp., Ecklonia cava, red algae, and others (Kafuku & Ikenoue, 1983).
As a rule, there are marked differences of the size, color and shape in three mollusk species according to the environmental conditions of habitat such as feed and winterization period. There is a need to understand the genetic traits and composition of their molluskin order to evaluate exactly the patent genetic effect. Our authors perform clustering analyses to elucidate the genetic distances among three malacological species of Notoacmea concinna and Haliotis discus hannai from Tongyeong and Sulculus diversicolor supertexta from Jeju Island of the Korean peninsula. However, these kinds of Korean mollusk, which are recognized important biometrically (Kim & Chung, 1985: Kim et al., 1994), geographically (Choe & Kim, 1988), reproductively (Kim et al., 2012) as well as biochemically (Mahmoud et al., 2010) are not genetically studied or researched like other shellfishes.
Therefore, in the present study, genomic DNAs isolated from three mollusk species were analyzed by 7 oligonucleotides decamer primers in order to make out the genetic distances of the three species by investigating their genetic similarity and diversity.
MATERIALS AND METHODS
Muscle tissues were collected separately from three mollusk species of Notoacmea concinna and Haliotis discus hannai from Tongyeong and Sulculus diversicolor supertexta from Jeju Island of the Korean peninsula, respectively, as shown in Fig. 1. PCR analysis was carried out on DNA samples extracted from a total of 21 individuals using seven decamer oligonucleotides primers. DNA extraction should be carried out according to the separation and extraction methods (Song & Yoon, 2013). After several washings, lysis buffer I (155 mM NH4Cl; 10 mM KHCO3; 1 mM EDTA) was added to the samples, and the mixture tubes were gently inverted. Ice-cold 70% ethanol was added, and then the samples were centrifuged at 19,621 g for 5 minutes to extract the DNA from the lysates. The concentration of the extracted genomic DNA was measured by optical density at 260 nm by a spectrophotometer (Beckman Coulter, Buckinghamshire, UK). The DNA pellets were incubation-dried for 2 hrs, held at –40°C until analysis and then dissolved in the TE buffer (10 mM Tris-HCl, pH 8.0; 1 mM EDTA).
Amplification products were separated by electrophoresis in 1.4% agarose gels (Bioneer Corp., Daejeon, Korea) with TBE (0.09 M Tris, pH 8.5; 0.09 M borate; 2.5 mM EDTA), using 100 bp DNA ladder (Bioneer Corp., Daejeon, Korea) as DNA molecular weight marker and detected by staining with ethidium bromide. Seven primers, BION-55 (5’- GTCACGGACG-3’), BION-50 (5’-CAAGCGAGGA-3’), BION-75 (5’-GAGGTCCACA-3’), BION-35 (5’-AGCG GCTAGG-3’), BION-61 (5’-GACCGCTTGT-3’), BION-69 (5’-GCATCCACCA-3’) and BION-66 (5’-TGGTGG ACCA-3’) were shown to generate the unique shared loci to each species and shared loci by the three species which could be clearly scored. PCR was performed using Programmable DNA Thermal Cycler (MJ Research Inc., Waltham, MA, USA). Similarity matrix including bandsharing values (BS) between different individuals in the three mollusk species was generated according formula of Jeffreys & Morton (1987), Yoke-Kqueen & Radu (2006) and Yoon & Kim (2004). A hierarchical clustering tree was constructed using similarity matrices to generate a dendrogram, which was facilitated by the Systat version 10 (SPSS Inc., Chicago, IL, USA).
RESULTS AND DISCUSSION
Genomic DNAs isolated from three mollusk species obtained in Tongyeong and Jeju Island, were amplified at several times by PCR reactions. The amplified products were separated by agarose gel electrophoresis (AGE) with oligonucleotide decamer primers and stained by ethidium bromide. The complication of the banding patterns was diverse spectacularly between the primers and two localities, as shown in Fig. 2. Based on the average bandsharing values of all samples, the similarity matrix ranged from 0.597 to 0.879 in the NC species, from 0.648 to 0.907 in the SDS species and from 0.694 to 0.884 in the HDH species, as illustrated in Table 1. The bandsharing value between individuals no. 08 and no. 09 was 0.907, which was the highest value identified within the SDS species. Accordingly, in this study, the size of the DNA fragments varied wildly, from 100 to 1,600 bp. 236 specific loci, with an average of 56.3 per primer, were identified in the NC species. 142 specific loci, with an average of 44.7 per primer, were identified in the SDS species, as illustrated in Table 2. Many researchers studied the sizes of DNA fragments in the PCR profiles of five species of Eastern Pacific abalone (genus Haliotis) (Muchmore et al., 1998), blacklip abalone (Haliotis rubra) (Huang et al., 2000), the brittle star (Amphiura filiformis) (McCormack et al., 2000), turtle leg (Pollicipes mitella) (Song & Yoon, 2013) and marsh clams (Corbicula spp.) (Yoon & Kim, 2003). Especially, 126 numbers of shared loci by the three species, with an average of 18 per primer, were observed among the three species, as illustrated in Table 3. The decamer primer BION-50 generated 49 unique loci to each species in the HDH species. Especially, the decamer primer BION-75 generated 7 unique loci to each species, which were identifying each species in the SDS species. Interestingly, the primer BION-50 detected 42 shared loci by the three species, major and/or minor fragments of sizes, which were identical in all samples. As regards average bandsharing value (BS) results, individuals from HDH species (0.829) exhibited higher bandsharing values than did individuals from NC species (0.780) (P< 0.05), as illustrated in Table 4.
In this study, the dendrogram obtained by the seven decamer primers indicates three genetic clusters: cluster 1 (CONCINNA 01~CONCINNA 07), cluster 2 (SUPERTEXTA 08~SUPERTEXTA 14), cluster 3 (HANNAI 15~HANNAI 21), as shown in Fig. 3. The shortest genetic distance that displayed significant molecular differences was between individuals 08 and 09 from the SDS species (genetic distance = 0.041), while the longest genetic distance among the twenty-one individuals that displayed significant molecular differences was between individuals NC no. 05 and HDH no. 21 (genetic distance = 0.627). Comparatively, individuals of HDH species were fairly closely related to that of SDS species, as shown in the hierarchical dendrogram of genetic distances. PCR fragments discovered in this study may be useful as a DNA marker. In invertebrates, cluster analysis of the pairwise population matrix, generated from genetic data, showed that geographically close populations tended to cluster together in the blacklip abalone (Huang et al., 2000). The potential of oligonucleotides amplified polymorphic DNAs to identify diagnostic markers for species and population identification in shellfish (McCormack et al., 2000; Kim et al., 2004; Park et al., 2005; Song & Yoon, 2013) has also been well established. Three mollusk species can be clearly distinguished by PCR-based approach. Therefore, this method can also be applied to other species of mollusk and make technically-convenient the analysis of many samples in a short time. In general, the species classification of three mollusk species is based on morphological variations in shell type, shell color, shell length, feet length and shell body weight (Chenyambuga et al., 2004). It is assumed that differences in such traits reflect distinct origins or genetic individuality (Chenyambuga et al., 2004). In future, additive researches should be in progress for more insightful species identifycation in Korean three mollusk species.