2013
DOI: 10.3390/ijms141123153
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Tetra-Repeat Microsatellite Markers for the Masu Salmon (Oncorhynchus masou masou) and Its Application in Cross-Subspecies Amplification

Abstract: 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 st… Show more

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Cited by 4 publications
(2 citation statements)
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“…For the 38 populations, selected mainly by sample size within populations (Table ), microsatellite DNA analysis was carried out using 13 loci: OMAS‐3, OMAS‐4, OMAS‐5, OMAS‐10, OMAS‐18 (Yamamoto, Kurokawa, Sekino, Yasuike, & Saitoh, ), OMM‐1311, OMM‐1344 (Palti, Fincham, & Rexroad, ), Ssa‐197 (O'Reilly, Hamilton, McConnel, & Wright, ), One‐111 (Olsen, Wilson, Kretschmer, Jones, & Seeb, ), Omy‐325 (Olsen, Wenburg, & Bentzen, ) Oma‐02, Oma‐3ke and Ots‐520 (Noguchi, Ikeda, Nakajima, & Taniguchi, ). After conjugating 6‐FAM, HEX, NED or PET fluorescent dyes to the 5′ end of each forward primer with tailed reverse primer (Thermo Fisher Scientific, Inc.), we analysed three multiplex PCR sets (Set‐A: OMAS‐3, OMAS‐4, OMAS‐5, OMAS‐10 and OMAS‐18; Set‐B: Oma‐02, Oma‐3ke, Ots‐520, Omy‐325 and OMM‐1311; Set‐C: OMM‐1344, One‐111 and Ssa‐197) using a Type‐it Microsatellite PCR Kit (Qiagen, Inc.).…”
Section: Methodsmentioning
confidence: 99%
“…For the 38 populations, selected mainly by sample size within populations (Table ), microsatellite DNA analysis was carried out using 13 loci: OMAS‐3, OMAS‐4, OMAS‐5, OMAS‐10, OMAS‐18 (Yamamoto, Kurokawa, Sekino, Yasuike, & Saitoh, ), OMM‐1311, OMM‐1344 (Palti, Fincham, & Rexroad, ), Ssa‐197 (O'Reilly, Hamilton, McConnel, & Wright, ), One‐111 (Olsen, Wilson, Kretschmer, Jones, & Seeb, ), Omy‐325 (Olsen, Wenburg, & Bentzen, ) Oma‐02, Oma‐3ke and Ots‐520 (Noguchi, Ikeda, Nakajima, & Taniguchi, ). After conjugating 6‐FAM, HEX, NED or PET fluorescent dyes to the 5′ end of each forward primer with tailed reverse primer (Thermo Fisher Scientific, Inc.), we analysed three multiplex PCR sets (Set‐A: OMAS‐3, OMAS‐4, OMAS‐5, OMAS‐10 and OMAS‐18; Set‐B: Oma‐02, Oma‐3ke, Ots‐520, Omy‐325 and OMM‐1311; Set‐C: OMM‐1344, One‐111 and Ssa‐197) using a Type‐it Microsatellite PCR Kit (Qiagen, Inc.).…”
Section: Methodsmentioning
confidence: 99%
“…These methods are laborious and difficult to use. With technological advances, such as next generation sequencing [14,15,16], the emerging sequencing platforms now allows us to quickly achieve a large number of SSR markers [17,18]. In this study, we utilized shotgun 454 pyrosequencing technology to isolate SSR markers from the C. coggygria genome.…”
Section: Introductionmentioning
confidence: 99%