Evidence map›Paper›PMID 39708186›Full record

ArticleMolecular biology reports2024

Multiplex panels of SNP markers based on single-base primer extension in the west Pacific pen shell Atrina lischkeana (Clessin, 1891).

Masashi Sekino, Reiichiro Nakamichi, Daisuke Ojima, Atsushi Ito

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 authors.

Masashi SekinoBioinformatics and Biosciences Division, Fisheries Resources Institute, Japan Fisheries Research and Education Agency, 2-12-4 Fuku-Ura, Kanazawa, Yokohama, Kanagawa, 236-8648, Japan. sekino_masashi31@fra.go.jp.
Reiichiro NakamichiBioinformatics and Biosciences Division, Fisheries Resources Institute, Japan Fisheries Research and Education Agency, 2-12-4 Fuku-Ura, Kanazawa, Yokohama, Kanagawa, 236-8648, Japan.
Daisuke OjimaProduction Engineering Division, Miyako Field Station, Fisheries Technology Institute, Japan Fisheries Research and Education Agency, 4-9-1 Miyako, Iwate, 027-0097, Japan.
Atsushi ItoProduction Engineering Division, Momoshima Field Station, Fisheries Technology Institute, Japan Fisheries Research and Education Agency, 1760 Momoshima, Onomichi, Hiroshima, 722-0061, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs part of stock enhancement programs for marine fishery species, the stocking of hatchery-produced seedlings into sea areas has been implemented worldwide. DNA markers are vital for responsible stock enhancement practices that aim to conserve the genetic diversity of recipient wild populations. We report novel single-nucleotide polymorphism (SNP) markers and multiplex SNP panels developed for the west Pacific pen shell Atrina lischkeana (Clessin, 1891), a large bivalve that is expected to be a subject of stock enhancement activity as the natural resource has dwindled, especially in Japan. METHODS AND

resultsOn the basis of single-base primer extension combined with MALD-TOF/MS analysis, we developed 218 SNP markers across eight multiplex SNP panels, which allowed genotyping of specimens from two wild A. lischkeana populations. However, our parentage analysis for a captive-bred population sample revealed that 21 of the 218 markers exhibited non-Mendelian patterns of allelic transmission in parent-offspring trios. We verified that the inheritance of undetectable null alleles caused almost all the aberrant allelic transmissions.

conclusionsThe developed markers will be of significant use in dealing with issues related to the stock enhancement of A. lischkeana, such as the monitoring of genetic diversity of hatchery stocks and the evaluation of impacts of stocking upon the genetic makeup of recipient wild populations, although caution is warranted especially when the 21 markers with unexpected patterns of allelic segregation are applied to field samples. Additionally, the markers can be analyzed in other targeted genotyping platforms.

Indexed as

Polymorphism, Single NucleotideAllelesAnimalsBivalviaDNA PrimersGenetic MarkersGenetic VariationGenotypeGenotyping TechniquesJapanDNA PrimersGenetic MarkersMassARRAYParentageRADSingle-nucleotide polymorphism

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.