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Development and characterization of twelve microsatellite loci for Amolops ricketti using next-generation sequencing

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Abstract

Amphibian populations have decreased dramatically because of human disturbance. To better conserve and manage native or wild populations of Amolops ricketti, 12 novel microsatellite loci were developed using high-throughput sequencing. The number of alleles ranged from 2 to 19, with an average of 7.67 alleles per locus. The observed and expected heterozygosity ranged from 0.42 to 1.00 (average 0.81) and from 0.51 to 0.95 (average 0.76), respectively. The polymorphism information content per locus ranged from 0.38 to 0.92 (average 0.69). These polymorphic microsatellite markers will contribute to the assessment of population structure, gene flow and genetic differentiation in A. ricketti.

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References

  1. Fei L, Ye C, Jiang J (2012) Colored atlas of Chinese amphibians and their distributions. Sichuan Publishing House of Science & Technology, Chengdu

    Google Scholar 

  2. Wang H, Ran R, Yu H, Yu Z, Hu Y, Zheng H, Wang D, Yang F, Liu R, Liu J (2012) Identifification and characterization of antimicrobial peptides from skin of Amolops ricketti (Anura: Ranidae). Peptides 33:27–34

    Article  Google Scholar 

  3. Zhang B, Zhang X, Yang Y, Hu Y, Wang H (2018) Identification and functional analysis of novel Bradykinin-related peptides (BRPs) from skin secretions of five Asian frogs. Protein J 37:324–332

    Article  CAS  Google Scholar 

  4. Lyu Z-T, Huang L-S, Wang J, Li Y-Q, Chen H-H, Qi S, Wang Y-Y (2019) Description of two cryptic species of the Amolops ricketti group (Anura, Ranidae) from southeastern China. ZooKeys 812:133–156

    Article  Google Scholar 

  5. Wu Y-H, Yan F, Stuart BL, Prendini E, Suwannapoom C, Dahn HA, Zhang B-L, Cai H-X, Xu Y-B, Jiang K, Chen H-M, Lemmon AR, Lemmon EM, Raxworthy CJ, Orlov NL, Murphy RW, Che J (2020) A combined approach of mitochondrial DNA and anchored nuclear phylogenomics sheds light on unrecognized diversity, phylogeny, and historical biogeography of the torrent frogs, genus Amolops (Anura: Ranidae). Mol Phylogenetics Evol 148:106789

    Article  Google Scholar 

  6. Zeng Z, Liang D, Li J, Lyu Z, Wang Y, Zhang P (2020) Phylogenetic relationships of the Chinese torrent frogs (Ranidae: Amolops) revealed by phylogenomic analyses of AFLP-capture data. Mol Phylogenetics Evol 146:106753

    Article  Google Scholar 

  7. Lu B, Bi K, Fu J (2014) A phylogeographic evaluation of the Amolops mantzorum species group: cryptic species and plateau uplift. Mol Phylogenetics Evol 73:40–52

    Article  Google Scholar 

  8. Van Dijk PP, Bain R, Lau MWN, Zhao E, Gu H (2004) Amolops ricketti. The IUCN Red List of Threatened Species 2004:e.T58224A11752348. https://doi.org/10.2305/IUCN.UK.2004.RLTS.T58224A11752348.en. Accessed 25 Mar 2020

  9. Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, New York

    Google Scholar 

  10. Thiel T, Michalek W, Varshney RK, Graner A (2003) Exploiting EST databases for the development and characterization of gene-derived SSR-markers in barley (Hordeum vulgare L.). Theor Appl Genet 106:411–422

    Article  CAS  Google Scholar 

  11. Untergasser A, Cutcutache I, Koressaar T, Ye J, Faircloth BC, Remm M, Rozen SG (2012) Primer3-new capabilities and interfaces. Nucleic Acids Res 40(15):e115

    Article  CAS  Google Scholar 

  12. Koressaar T, Remm M (2007) Enhancements and modifications of primer design program Primer3. Bioinformat Appl Note 23(10):1289–1291

    Article  CAS  Google Scholar 

  13. Kalinowski ST, Taper ML, Marshall TC (2007) Revising how the computer program CERVUS accommodates genotyping error increases success in paternity assignment. Mol Ecol 16:1099–1106

    Article  Google Scholar 

  14. Rousset F (2008) Genepop’007: a complete re-implementation of the genepop software for Windows and Linux. Mol Ecol Resour 8:103–106

    Article  Google Scholar 

  15. Van Oosterhout C, Hutchinson WF, Wills DPM, Shipley P (2004) MICRO-CHECKER: software for identifying and correcting and genotyping errors in microsatellite data. Mol Ecol Notes 4:535–538

    Article  Google Scholar 

Download references

Acknowledgments

This work was supported by Zhejiang Provincial Natural Science Foundation of China (L19C030005, LQ14C040001) and the National Natural Science Foundation of China (31400472).

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Correspondence to Yu Wang.

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The authors declare that they have no conflict of interest.

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This research was approved by the Gutian Mountain National Nature Reserve Authority and Ethics Committee of Zhejiang Normal University, and it was conducted under Law of the People’s Republic of China on the Protection of Wildlife (August 28, 2004).

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Wei, N., Kan, X., Shao, C. et al. Development and characterization of twelve microsatellite loci for Amolops ricketti using next-generation sequencing. Mol Biol Rep 47, 6435–6437 (2020). https://doi.org/10.1007/s11033-020-05654-6

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  • DOI: https://doi.org/10.1007/s11033-020-05654-6

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