The gDNA isolated from Cyclina sinensis from Gochang (GOCHANG), Incheon (INCHEON) and a Chinese site (CHINESE), were amplified by PCR. Here, the seven oligonucleotide decamer primers (BION-66, BION-68, BION-72, BION-73, BION-74, BION-76, and BION-80) were used to generate the unique shared loci to each population and shared loci by the three cyclina clam populations. As regards multiple comparisons of average bandsharing value results, cyclina clam population from Chinese (0.763) exhibited higher bandsharing values than did clam from Incheon (0.681). In this study, the dendrogram obtained by the seven decamer primers indicates three genetic clusters: cluster 1 (GOCHANG 01~GOCHANG 07), cluster 2 (INCHEON 08~INCHEON 14), cluster 3 (CHINESE 15~CHINESE 21). The shortest genetic distance that displayed significant molecular differences was between individuals 15 and 17 from the Chinese cyclina clam (0.049), while the longest genetic distance among the twenty-one cyclina clams that displayed significant molecular differences was between individuals GOCHANG no. 03 and INCHEON no. 12 (0.575). Individuals of Incheon cyclina clam population was somewhat closely related to that of Chinese cyclina clam population. In conclusion, our PCR analysis revealed a significant genetic distance among the three cyclina clam populations.

The authors have investigated three species of Clupeidae such as herring, Korean anchovy and large-eyed herring, belonging to the order Clupeiformes. The fish is also indigenous to some parts of the southern regions of the West Sea. Fishes are the most popular marine products in Korea because of their taste and nutritional value, and Koreans consume them in large quantities. Especially, Korean anchovy and large-eyed herring are widely distributed in the entirety of brackish-water habitats and seawater areas of the West Sea in the Korean Peninsula, as well as in several areas in China. However, in spite of their economic and scientific consequences, a little information currently exist regarding the physiological and ecological levels only of crab species in Korea. During the last two decades, environmental contamination and various environmental disruptions by industries and city sewage, have threatened the coastal fisheries, and then reduction of individual number of this fish is an increasing trend in the 2000s. This study attempt is to elucidate the genetic distances within and between herring, Korean anchovy and large-eyed herring population from the West Sea. Three species of herring (C. pallasii), Korean anchovy (C. nasus) and large-eyed herring (H. zunashi) were obtained in close vicinity to the West Sea in Korea. Three species of fish muscle was collected in sterile tubes, placed on ice immediately, and stored under refrigeration until needed. Genomic DNA was extracted and purified under the conditions described previously (Yoon and Kim, 2004). The degree of variability was calculated by use of the Dice coefficient (F), which is given by the formula: F = 2nab / (na+nb), where nab is the number of bands shared between the samples a and b, na is the total number of bands for sample a and nb is the total number of bands for sample b (Jeffreys and Morton, 1987; Yoke-Kqueen and Radu, 2006). Euclidean genetic distances within-and between-species were also calculated by complete linkage method with the help of the hierarchical dendrogram program Systat version 10. The genomic DNA isolated from herring (C. pallasii), Korean anchovy (C. nasus) and large-eyed herring (H. zunashi) in the West Sea, were amplified several times by PCR reaction. The dendrogram obtained by the seven primers indicates three genetic clusters as shown in Fig. 1. The hierarchical dendrogram indicates three main branches: cluster 1 (PALLASII 01, 02, 03, 04, 06 and 07), cluster 2 (NASUS 08, 09, 10 and 11), and cluster 3 (NASUS 12, 13 and 14, ZUNASHI 15, 16, 17, 18, 19, 20 and 21, PALLASII 05). The genetic distance among the three fish species ranged from 0.018 to 0.318. In three fish population, the shortest genetic distance displaying significant molecular difference was between individual PALLASII no. 03 and PALLASII no. 02 (0.018). Ultimately, individual no. 05 of the PALLASII herring was most distantly related to PALLASII no. 06 (genetic distance = 0.318). From what has been said above, the potential of this PCR analysis to identify diagnostic markers for the identification of three fish populations has been demonstrated. Generally speaking, this PCR analysis method has been applied to identify specific markers particular to line, species and geographical population, as well as genetic diversity/polymorphism in diverse species of organisms (McCormack et al. 2000; Yoon and Kim 2003).

As in the O. mykiss electrophoretic profiles of RNA, the signals of each RNA sample from 9 individual tissues such as liver, muscle, brain, heart, pituitary gland, kidney, intestine, spleen and gill similar to positive control were obtained. The tissue distributions of the complimentary DNA (cDNA) of O. mykiss four genes were analyzed using quantitative real-time PCR with primer sets for tissue expression analysis. In this rainbow trout species, author obtained bands of various sizes, ranged from 700 bp to 1,400 bp. A dissociation curve was made at the end of each run to make sure that there was no non-specific amplification. Supplementarily, the Ct of each DNA was compared. The Ct values of vinculin with rainbow trout tissues were determined in a manner similar to those for agouti-related protein (AgRP) and melanocortin receptors (MC4R I and MC4R II). Further, obtained Cts for standard curve of each DNA were affected by specific product (vinculin, AgRP and MC4R II genes). After several experiments with four individual genes of rainbow trout, author estimated a variation ratio of the mean Ct value of the DNA extracted using the comparative CTt method was 37.27, and the standard deviation was 5.33. The correlation coefficient between the Ct values and the concentration of cDNA was -0.98, -0.99, -0.91 and -0.86, respectively (vinculin, AgRP, MC4R I and MC4R II genes). Since this correlation showed high linearity, the straight line obtained was used as a standard for the O. mykiss tissues reared in aquarium. A PCR efficiency of 100% is ideally achieved when the slopes are close to the theoretical value of -3.31. According to quantification method, the results of quantification are strongly affected by the DNA fragmentation. The size of most DNA fragments obtained from various tissues of rainbow trout used in the experiment was approximately 100 bp. According to the four slopes, an efficiency of nearly 100% was estimated for four genes detection methods. Additionally, further analysis with more individuals and primers will be required to fully establish optimization in rainbow trout.

Hairtail, Trichiurus lepturus, ecologically warm water fish species, belonging to family Trichiuridae, widely distributed on the coast of the West Sea, South Sea and Jeju island in the Korean Peninsula and the several sea areas in China under the natural ecosystem. The food consumption of this species has increased considerably in various types of restaurants (including restaurants specializing in serving hairtails roasted and soy-sauce glazed cutlass fish with radish or other vegetables) for a long time. However, in spite of their economic and scientific consequences, a little information currently exist regarding the physiological and ecological levels only of hairtail species in Korea. Only the biological fisheries feature, distribution and migration of hairtail, Trichiurus lepturus, in Korean waters were in vestigated (Kimatal, 1998; Parketal, 2002). Lately, imported hairtail have been changed into endemic hairtail because of high margin. In the present study, to elucidate the genetic distances and differences among geographical hairtail, Trichiurus lepturus, populations, we performed a clustering analysis of two hairtail populations collected from Korea and China. Muscle tissues were collected separately from hairtail, Trichiurus lepturus, in dividuals from Korea in the Yellow Sea and China in the East Sea, respectively. RAPD-PCR analysis was performed on DNA samples extracted from a total of 44 (specimen numbers for duplicate experiments) individuals using eight arbitrarily selected primers of two decades of different decamer primers. Hairtail muscle was collected in sterile tubes, immediately placed on dry ice, and stored at －40℃ until the genomic DNA extraction. Genomic DNA was extracted and purified under the conditions described previously (Yoon and Kim, 2004). The degree of variability was calculated by use of the Dice coefficient (F), which is given by the formula: F = 2 nab/(na+nb), where nab is the number of bands shared between the samples a and b, na is the total number of bands for sample a and nb is the total number of bands for sample b (Jeffreys and Morton, 1987; Yoke-Kqueen and Radu, 2006). Euclidean genetic distances within- and between-populations were also calculated using the hierarchical dendrogram program Systat ver.10 (SPSS Inc., Chicago, IL, USA). The random primers OPA-07, OPA-20, OPB-14, OPB-15, OPB-17, OPB-18, OPD-16 and URP-07 showed common, polymorphic and specific bands produced using each primer to amplify genomic DNA isolated from the muscle of individuals. Accordingly, PCR analysis generated on the RAPD data showed that the geographic hairtail population from Korea in the West Sea was more or less separated from geographic hairtail population from China in the South Sea. The hierarchical dendrogram resulted from reliable four primers, indicating three genetic clusters composed of group 1 (Korean No. 1～11) and group 2 (Chinese No. 12～22). The genetic distances between two geographic populations ranged from 0.038 to 0.476. Individual No. 09 within hairtail population from Korea was genetically closely related with No. 06 (genetic distance = 0.104). The longest genetic distance (0.476) displaying significant molecular difference was also between individual No. 01 within hairtail population from Korea and No. 22 from Chinese. In the present study, RAPD-PCR analysis has revealed significant genetic distances between two hairtail population pairs. High levels of genetic polymorphisms and the existence of population differentiation between two hairtail populations showed RAPD-PCR approach is one of the suitable tools for individuals and/or population biological DNA studies.