Abstract

Pen shell (Atrina pectinata) is a popular food source with a high commercial value in a number of Asian Pacific areas. The natural A. pectinata population has been declining continuously over the past several decades. Microsatellite DNA markers are a useful DNA-based tool for monitoring the genetic variation of pen shell populations. In this study, 20 polymorphic microsatellite (MS) DNA markers were identified from a partial genomic pen shell DNA library enriched in CA repeats, and used to compare allelic variation between wild and hatchery pen shell populations in Korea. A total of 438 alleles were detected at the 20 MS loci in the two populations. All loci were easily amplified and demonstrated allelic variability, with the number of alleles ranging from 5 to 35 in the wild population and from 5 to 22 in the farmed population. The average observed and expected heterozygosities were 0.69 and 0.82, respectively, in the hatchery samples and 0.69 and 0.83, respectively, in the wild samples. Statistical analysis of fixation index (FST) and analysis of molecular variance (AMOVA) showed minor, but significant, genetic differences between the wild and hatchery populations (FST = 0.0106, CI95% = 0.003–0.017). These microsatellite loci may be valuable for future aquaculture and population genetic studies for developing conservation and management plans. Further studies with additional pen shell samples are needed to conclusively determine the genetic diversity between the wild and hatchery populations.

Highlights

  • Marine shells of the Pinnidae family are a popular food source with a high commercial value in a number of Asian Pacific areas

  • More than 400 white colonies were obtained from the transformation with the Korean pen shell (CA)n-enriched genomic DNA library, 150 of which were screened by polymerase chain reaction (PCR) for the presence of a repeat-containing insert

  • Genetic studies on pen shell with microsatellite DNA markers are very rare with only two existing reports on the development of new microsatellites [11,12]

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Summary

Introduction

Marine shells of the Pinnidae family are a popular food source with a high commercial value in a number of Asian Pacific areas. With the rapid development of pen shell aquaculture and breeding projects, molecular markers for studying the genetic variation can help elucidate the genetic differences among wild populations, assess genetic variation within captive stocks, and determine the genetic impacts of aquaculture on wild populations, thereby promoting sustainable aquaculture Because of their high degree of variability, microsatellite (MS) DNA markers or simple sequence repeats (SSRs) are molecular markers that are suitable tools for monitoring changes in the genetic variation of farmed stocks, assigning parentage, and evaluating the genetic diversity and structure of various marine species for the improvement of fisheries and resource conservation [7,8,9,10].

Microsatellite Markers Isolation
Genetic Variation within Populations
Genetic Diversity between the Wild and Hatchery Populations
Sample Collection and DNA Extraction
Genomic Library Construction and Microsatellite Sequencing
Primer Design and Allele Scoring
Sample Comparisons
Conclusions
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