2009
DOI: 10.1007/s12686-009-9148-y
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Isolation and characterization of thirteen microsatellite markers for the rabbitfish, Siganus fuscescens

Abstract: The mottled spinefoot, Siganus fuscescens, is an economically important rabbitfish species widely distributed in shallow waters throughout the Indo-Pacific. We describe methods for the identification of thirteen novel microsatellite markers for S. fuscescens using an enrichment protocol. The loci were screened in 126 individuals, revealing moderate to high levels of polymorphism with 5 to 28 alleles per locus and observed heterozygosity ranging from 0.111 to 0.921. No significant deviations from HardyWeinberg … Show more

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Cited by 3 publications
(3 citation statements)
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“…Genomic DNA was extracted using DNeasy Blood and Tissue kits (QIAGEN, Valencia, CA, USA). Samples were genotyped at five microsatellite loci originally designed for the S. spinus congener S. fuscescens (Ravago‐Gotanco et al 2010). The loci used in this study were Sfus‐8, Sfus‐9, Sfus‐56, Sfus‐98, and Sfus‐113 .…”
Section: Methodsmentioning
confidence: 99%
“…Genomic DNA was extracted using DNeasy Blood and Tissue kits (QIAGEN, Valencia, CA, USA). Samples were genotyped at five microsatellite loci originally designed for the S. spinus congener S. fuscescens (Ravago‐Gotanco et al 2010). The loci used in this study were Sfus‐8, Sfus‐9, Sfus‐56, Sfus‐98, and Sfus‐113 .…”
Section: Methodsmentioning
confidence: 99%
“…Individuals were genotyped at 12 microsatellite markers previously developed for S . fuscescens : Sfus6 , Sfus8 , Sfus9 , Sfus21 , Sfus22 , Sfus56 , Sfus76 , Sfus95 , Sfus97 , Sfus98 , Sfus113 , and Sfus167 [ 24 ]. Microsatellite DNA fragments were PCR-amplified in four separate multiplex reactions.…”
Section: Methodsmentioning
confidence: 99%
“…Amplification conditions consisted of 94°C for 90 s, 38 cycles of 94°C for 30 s, locus-specific annealing temperatures for 30 s, 72°C for 60 s and a final extension at 72°C for 25 minutes. Annealing temperatures, fluorescent label-primer combinations, and pooling of amplified microsatellite loci for fragment analysis have been described elsewhere [ 24 ]. Amplified fragments were combined with an internal size standard, GeneScan TM 500 LIZ TM , Hi-Di TM formamide (Applied Biosystems Inc., Carlsbad CA) and deionized water to a final volume of 10 μL.…”
Section: Methodsmentioning
confidence: 99%