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ArticleMolecular biology reports2025

Microsatellite DNA markers for paternity identification in the hermaphroditic barnacle Chthamalus challengeri Hoek.

Masami M Tamechika, Yoichi Yusa, Shingo Akita, Masashi Sekino

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Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Masami M TamechikaGraduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato- cho, Hakodate, Hokkaido, 041-8611, Japan. tamechi555@gmail.com.
Yoichi YusaFaculty of Science, Nara Women's University, Nara, 630-8506, Japan.
Shingo AkitaGraduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato- cho, Hakodate, Hokkaido, 041-8611, Japan.
Masashi SekinoFisheries Resources Institute, Japan Fisheries Research and Education Agency, 2-12-4 Fuku-ura, Kanazawa, Yokohama, Kanagawa, 236-8648, Japan.

Funding

Japan Science and Technology Agency JPMJSP2119Japan Society for the Promotion of Science 24K02100
6 · The paper itself

Abstract

backgroundSimultaneously hermaphroditic animals allocate resources to both male and female reproductive functions (sex allocation). Although male reproductive success is a key factor in determining sex allocation, it is seldom evaluated in marine hermaphrodites, as it requires the development of suitable DNA markers to trace paternity. The sessile, simultaneously hermaphroditic barnacle Chthamalus challengeri Hoek, 1883 is widely found along rocky intertidal shores in the northwestern Pacific. In this report, we describe microsatellite DNA markers for C. challengeri and multiplex panels of the markers, which can be used to reveal reproductive success via paternity identification. METHODS AND

resultsWe obtained 632 microsatellite sequences by using next-generation sequencing. We examined 189 primer sets, of which 11 passed our filtering criteria. Through simulation analysis, we demonstrated that these primers can be used as microsatellite markers for accurate paternity determination. Additionally, we established five multiplex panels by using all the developed markers.

conclusionsWe developed 11 microsatellite DNA markers for paternity analysis. These markers, which exhibited a moderate to high degree of polymorphism in a population sample, should be useful in paternity inference. We also established multiplex panels for the markers, thus enabling low-cost and efficient analysis. These advancements will enable us to evaluate male reproductive success and contribute to a better understanding of sex allocation in C. challengeri and in hermaphroditic barnacles more broadly.

Indexed as

Hermaphroditic OrganismsMicrosatellite RepeatsThoracicaAnimalsFemaleGenetic MarkersHigh-Throughput Nucleotide SequencingMalePaternityPolymorphism, GeneticReproductionGenetic MarkersHermaphroditismParentageReproductive successSex allocationSimple sequence repeatSimple tandem repeat

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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.