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Int. J. Mol. Sci. 2013, 14(11), 23153-23159; doi:10.3390/ijms141123153

Tetra-Repeat Microsatellite Markers for the Masu Salmon (Oncorhynchus masou masou) and Its Application in Cross-Subspecies Amplification
Shoichiro Yamamoto 1,*, Tadahide Kurokawa 2, Masashi Sekino 3, Motoshige Yasuike 3 and Kenji Saitoh 3
National Research Institute of Aquaculture, Fisheries Research Agency, Nikko, Tochigi 321-1661, Japan
Tohoku National Fisheries Research Institute, Fisheries Research Agency, Shiogama, Miyagi 985-0001, Japan
National Research Institute of Fisheries Science, Fisheries Research Agency, Yokohama, Kanagawa 236-8648, Japan
Author to whom correspondence should be addressed; Tel.: +81-288-55-0055; Fax: +81-288-55-0064.
Received: 26 September 2013; in revised form: 11 November 2013 / Accepted: 12 November 2013 / Published: 21 November 2013


: We developed tetranucleotide-repeat microsatellite markers for the masu salmon (Oncorhynchus masou) complex. 454 pyrosequencing was used to discover repeat motifs, and seven polymorphic microsatellite-primer sets were identified. The number of alleles detected at each locus ranged from four to 24 and the expected heterozygosity varied from 0.57 to 0.92. Cross-subspecies amplification for O. m. masou, O. m. ishikawae and O. m. subsp. was successful. These microsatellites can be utilized in studies of genetic structure, genetic diversity, and intra- and inter-subspecific hybridization, making a contribution to conservation and management of the Oncorhynchus masou complex.
short tandem repeat; simple sequence repeat; 454 pyrosequencing; next-generation sequencer; Oncorhynchus masou

1. Introduction

The masu salmon (Oncorhynchus masou) subspecies-complex (Salmonidae) is widely distributed in Far East Asia [1] and consists of four subspecies [2,3]. The subspecies are based on zoogeographic patterns and morphological characteristics; O. m. masou (Japanese name: sakura-masu), O. m. ishikawae (amago), O. m. subsp. (biwa-masu), and O. m. formosanus. O. m. masou and O. m. ishikawae have allopatric distributions, and are distinguishable by the spot-color pattern on their lateral sides: the former has black-spots while the latter has red-spots with sparse black-spots. O. m. subsp. is endemic to the Lake Biwa basin, central Honshu Island, Japan. Mitochondrial DNA analysis indicated that O. m. subsp. has a sister relationship with O. m. masou and O. m. ishikawae [4]. O. m. formosanus, which is endemic to Taiwan, has the world’s southernmost distribution among the native salmonid fishes.

The masu salmon subspecies-complex supports important recreational and commercial fisheries throughout the Japanese archipelago. Hatchery-reared masu salmon have been released into many rivers in Japan to enhance the fish stocks available to local fishermen and recreational anglers. However, their genetic integrities and diversities have been ignored, resulting in accelerated hybridizations between wild and hatchery fish within the subspecies [5,6] and among subspecies [7,8]. In addition, habitat fragmentations by artificial damming occur frequently in Japanese rivers, causing reduced population sizes and genetic diversities of salmonid populations [5,9,10]. O. m. subsp. is “near threatened (NT)” on the red list of the ministry of the environment, Japan (2007) [11]. O. m. formosanus is listed as an endangered species by the Taiwanese government, and as a critically endangered species by the International Union for Conservation of Nature (IUCN) [1214].

Several dinucleotide-type microsatellite markers for masu salmon have been reported [15]. At present, however, we do not know whether these loci can be used across the masu salmon subspecies-complex. In addition, it will be useful to develop microsatellite markers with larger repeat motifs which allow easier genotyping than dinucleotide microsatellites. In this study, we performed 454 pyrosequencing [GS-FLX+ System, 454 Life Sciences by Roche Diagnostics (Branford, CT, USA)] to isolate novel microsatellite markers from the O. m. masou genome, and evaluated their potential for conservation genetic applications, such as cross-subspecies amplifications and population genetic analyses.

2. Results and Discussion

Seven polymorphic microsatellite loci were isolated and deposited in GenBank (AB851460-AB851466; Table 1). The number of alleles detected at each locus ranged from four (OMAS-10) to 24 (OMAS-4) and the expected heterozygosity varied from 0.57 (OMAS-10) to 0.92 (OMAS-5). The intrapopulation diversities differed, with the mean number of alleles per population varying between 4.43 (Miya River: O. m. ishikawae) and 11.29 (Chitose River: O. m. masou), and the expected heterozygosity varied between 0.60 (Miya River) and 0.80 (Chitose River; Table 2). Among 27 Hardy-Weinberg equilibrium (HWE) tests, where OMAS-10 marker in O. m. ishikawae was omitted due to no allelic variation, six were significant after the false discovery rate correction of significant level for multiple comparisons. The observed departures, however, were neither locus nor population specific; therefore, we could not determine the cause of the HWE deviations. No marker pair showed evidence of departure from linkage equilibrium, indicating no significant allelic association between the markers. These microsatellites represent useful tools for population genetic applications, such as stock identification in the Oncorhynchus masou complex.

3. Experimental Section

3.1. Isolation of Microsatellite Markers

Total genomic DNA from O. m. masou (blood cell) was extracted by proteinase K digestion, phenol/chloroform extraction, and ethanol precipitation. We prepared a shotgun library from 1.0 μg of genomic DNA following the 454-Roche protocol. Pyrosequencing was conducted on one-fourth picotiter plate. We searched for microsatellites and microsatellite-flanking PCR primer sequences using Auto-Primer [16]. A 454 run generated 175,689 sequence reads (63,019,585 bp) from ca. 5.0 × 105 beads with clonally amplified DNA, resulting in 1937 contigs and 129,759 singletons. Auto-Primer proposed 242 PCR primer sets for tetra-nucleotide microsatellites. We selected 18 primer sets designed for amplification of “perfect-type” tetra-nucleotide repeats (i.e., repeat arrays without interruption by a non-repeat element); 11 were rejected because of poor amplification or difficulty in allele scoring. The remaining seven sets were applicable for estimation of polymorphism (Table 1).

3.2. PCR Amplification and Genotyping

Three wild population samples (O. m. masou from the Chitose River, Hokkaido Island, Japan; O. m. ishikawae from the Miya River, central Honshu, Japan; and O. m. subsp. from Lake Biwa, central Honshu, Japan) and one hatchery-reared stock sample (O. m. masou from the Ohara River, northern Honshu, Japan) were used for polymorphism detection. After conjugating 6-FAM, HEX, NED or PET fluorescent dyes (Applied Biosystems, Life Technologies, Carlsbad, CA, USA) to the 5′-end of each forward primer, we performed multiplex PCR for the seven selected primer sets using a Qiagen multiplex PCR kit (Qiagen, Limburg, The Netherlands). The 10-μL reaction mixture contained 1× Qiagen multiplex PCR master mix, 0.2 μM of each primer, 2 μL of distilled water, and 1 μL of DNA solution. Amplifications were carried out in a GeneAmp PCR System 2700 thermal cycler (Applied Biosystems), according to the supplier’s instructions (Qiagen multiplex PCR kit; Qiagen): initial denaturation at 95 °C for 15 min; followed by 30 cycles of denaturation at 94 °C (30 s), annealing (60 °C, 90 s) and extension (72 °C, 60 s); with a final extension (60 °C, 30 min). PCR fragments and GeneScan 600LIZ size standards were resolved on an ABI PRISM 3730xl sequencer (Applied Biosystems, Life Technologies). Allele size was determined using GeneMapper v4.1 (Applied Biosystems, Life Technologies).

3.3. Data Analysis

Polymorphism statistics, including the observed/expected heterozygosities, were calculated in Arlequin v3.5 [17]. The Hardy-Weinberg equilibrium of markers/populations was tested using Fisher’s exact test with the Markov chain method (Markov chain steps: 105; Dememorization: 105). We also examined linkage equilibrium between markers (likelihood-ratio test: 104 permutations). Critical significance levels for multiple testing were adjusted following the false discovery rate [18].

4. Conclusions

We report the isolation and characterization of seven polymorphic microsatellite loci for the Oncorhynchus masou complex. All seven markers used were polymorphic. Cross-subspecies amplification for O. m. masou, O. m. ishikawae and O. m. subsp. was successful. These microsatellites can be utilized in studies of genetic structure, genetic diversity, and intra- and inter-subspecific hybridization, making a contribution to conservation and management of the Oncorhynchus masou complex.

Table 1. Tetra-nucleotide microsatellite markers for Oncorhynchus masou complex.
Table 1. Tetra-nucleotide microsatellite markers for Oncorhynchus masou complex.
MarkerMotif *1Primer sequences (5′-3′) *2Ta *3RA (bp) *4GenBank No.

*1Repeat counts are based on the individual from which the microsatellite-primer sequences were obtained;*2The forward primer of each primer set was 5′-end-labeled with 6-FAM (denoted as F-F), VIC (F-V), NED (F-N) or PET (F-P) fluorescent dye;*3Optimized annealing temperature.*4Range of allele sizes.

Table 2. Genetic diversity statistics for the three subspecies of Oncorhynchus masou.
Table 2. Genetic diversity statistics for the three subspecies of Oncorhynchus masou.
SubspeciesRiver/LakeStatistics of polymorphisms *1OMAS-3OMAS-4OMAS-5OMAS-7OMAS-10OMAS-14OMAS-18
Oncorhynchus masou masouChitose RiverHo0.860.930.730.900.500.670.31
HW_P0.120.01 *0.00 * *
Number of Alleles15171712387

Oncorhynchus masou ishikawaeMiya RiverHo0.460.830.750.24-0.600.15
HW_P1.000.00 *0.020.00 *-0.021.00
Number of Alleles5866123

Oncorhynchus masou subsp.Lake BiwaHo0.780.870.780.780.060.530.81
Number of Alleles914119277

Oncorhynchus masou masou (hatchery stock)Oohara RiverHo0.790.640.840.710.560.790.14
HW_P0.560.470.020.690.910.370.00 *
Number of Alleles7684343

Number of Alleles911118255

*1Ho: observed heterozygosity; HE: expected heterozygosity; HW_P: probability value of Hardy-Weinberg equilibrium (HWE) testing. Significant HWE departure after the false discovery rate correction of significance level for multiple comparisons is indicated by an asterisk; n: number of genotyped individuals.


We thank K. Kawamura, T. Kikko, S. Sato and A. Nawata for donating masu salmon samples. We also thank M. Yoshida and T. Ootsuka for their assistance with the DNA analysis. This study was supported by Grants-in-Aid for Scientific Research (Nos. 22510251 and 25450290 to S. Y., 25450295 to T. K.) from the Japan Society for the Promotion of Science.

Conflicts of Interest

The authors declare no conflict of interest.


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