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Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis

Chinese sturgeon (Acipenser sinensis) has been listed as a critically endangered species on the IUCN Red List and is an endemic fish of China. Five sets of duplex polymerase chain reactions (PCR) assays were developed with 10 tetranucleotide microsatellites for Chinese sturgeon. The size of CS57, ZH...

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Autores principales: Hu, Yacheng, Liu, Xueqing, Yang, Jing, Xiao, Kan, Wang, Binzhong, Du, Hejun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044248/
https://www.ncbi.nlm.nih.gov/pubmed/32103060
http://dx.doi.org/10.1038/s41598-020-60401-y
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author Hu, Yacheng
Liu, Xueqing
Yang, Jing
Xiao, Kan
Wang, Binzhong
Du, Hejun
author_facet Hu, Yacheng
Liu, Xueqing
Yang, Jing
Xiao, Kan
Wang, Binzhong
Du, Hejun
author_sort Hu, Yacheng
collection PubMed
description Chinese sturgeon (Acipenser sinensis) has been listed as a critically endangered species on the IUCN Red List and is an endemic fish of China. Five sets of duplex polymerase chain reactions (PCR) assays were developed with 10 tetranucleotide microsatellites for Chinese sturgeon. The size of CS57, ZHX43, ZHX69, AS105, ZHX51, AS074, ZHX2, AS078, AS026 and AS073 products in 184 Chinese sturgeon individuals ranged from 257–305, 191–241, 251–285, 172–244, 236–260, 169–209, 194–234, 92–176, 165–257 and 120–164, respectively. The observed allele number of the 10 microsatellites ranged from 7 to 16, and the total number of alleles was 106. The number of alleles per individual in CS57, ZHX43, AS105, AS074, AS078 and AS026 was 1–4. The number of alleles per individual in ZHX69, ZHX51, ZHX2 and AS073 was 2–4. The mean number of alleles per locus per individual ranged from 2.01–3.76. The expected heterozygosity (H(E)), observed heterozygosity (H(O)), polymorphic information content (PIC) and Shannon-Weiner diversity index (H′) ranged from 0.582 to 0.899, from 0.676 to 1, from 0.518 to 0.886 and from 1.034 to 2.34, respectively. Despite many advantages, the use of microsatellites as genetic analysis tools can be limited by the cost of the associated experiment. To solve this problem, this set of five duplex PCRs will provide tools that are more helpful, less expensive and less time consuming than others used for genetic analyses in Chinese sturgeon.
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spelling pubmed-70442482020-03-04 Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis Hu, Yacheng Liu, Xueqing Yang, Jing Xiao, Kan Wang, Binzhong Du, Hejun Sci Rep Article Chinese sturgeon (Acipenser sinensis) has been listed as a critically endangered species on the IUCN Red List and is an endemic fish of China. Five sets of duplex polymerase chain reactions (PCR) assays were developed with 10 tetranucleotide microsatellites for Chinese sturgeon. The size of CS57, ZHX43, ZHX69, AS105, ZHX51, AS074, ZHX2, AS078, AS026 and AS073 products in 184 Chinese sturgeon individuals ranged from 257–305, 191–241, 251–285, 172–244, 236–260, 169–209, 194–234, 92–176, 165–257 and 120–164, respectively. The observed allele number of the 10 microsatellites ranged from 7 to 16, and the total number of alleles was 106. The number of alleles per individual in CS57, ZHX43, AS105, AS074, AS078 and AS026 was 1–4. The number of alleles per individual in ZHX69, ZHX51, ZHX2 and AS073 was 2–4. The mean number of alleles per locus per individual ranged from 2.01–3.76. The expected heterozygosity (H(E)), observed heterozygosity (H(O)), polymorphic information content (PIC) and Shannon-Weiner diversity index (H′) ranged from 0.582 to 0.899, from 0.676 to 1, from 0.518 to 0.886 and from 1.034 to 2.34, respectively. Despite many advantages, the use of microsatellites as genetic analysis tools can be limited by the cost of the associated experiment. To solve this problem, this set of five duplex PCRs will provide tools that are more helpful, less expensive and less time consuming than others used for genetic analyses in Chinese sturgeon. Nature Publishing Group UK 2020-02-26 /pmc/articles/PMC7044248/ /pubmed/32103060 http://dx.doi.org/10.1038/s41598-020-60401-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hu, Yacheng
Liu, Xueqing
Yang, Jing
Xiao, Kan
Wang, Binzhong
Du, Hejun
Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title_full Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title_fullStr Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title_full_unstemmed Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title_short Development and characterization of a duplex PCR assay in Chinese sturgeon (Acipenser sinensis) for genetic analysis
title_sort development and characterization of a duplex pcr assay in chinese sturgeon (acipenser sinensis) for genetic analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044248/
https://www.ncbi.nlm.nih.gov/pubmed/32103060
http://dx.doi.org/10.1038/s41598-020-60401-y
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