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  4. Development of 16 novel EST-SSR markers for species identification and cross-genus amplification in sambar, sika, and red deer
 
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Development of 16 novel EST-SSR markers for species identification and cross-genus amplification in sambar, sika, and red deer

Journal
PLoS ONE
Journal Volume
17
Journal Issue
4 April
Date Issued
2022-04-01
Author(s)
Hsiao, Chen
Lin, Hsin Hung
Kang, Shann Ren
Hung, Chien Yi
Sun, Pei Yu
Yu, Chieh Cheng
Toh, Kok Lin
Yu, Pei Ju
YU-TEN JU  
DOI
10.1371/journal.pone.0265311
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/630058
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127435752&doi=10.1371%2fjournal.pone.0265311&partnerID=40&md5=3cb68a15a2924a8fc277f3fd6bc4b862
URL
https://api.elsevier.com/content/abstract/scopus_id/85127435752
Abstract
Deer genera around the globe are threatened by anthropogenic interference. The translocation of alien species and their subsequent genetic introgression into indigenous deer populations is particularly harmful to the species of greatest conservation concern. Products derived from deer, including venison and antler velvet, are also at risk of fraudulent labeling. The current molecular markers used to genetically identify deer species were developed from genome sequences and have limited applicability for cross-species amplification. The absence of efficacious diagnostic techniques for identifying deer species has hampered conservation and wildlife crime investigation efforts. Expressed sequence tag-simple sequence repeat (EST-SSR) markers are reliable tools for individual and species identification, especially in terms of cross-species genotyping. We conducted transcriptome sequencing of sambar (Rusa unicolor) antler velvet and acquired 11,190 EST-SSRs from 65,074 newly assembled unigenes. We identified a total of 55 unambiguous amplicons in sambar (n = 45), which were selected as markers to evaluate cross-species genotyping in sika deer (Cervus nippon, n = 30) and red deer (Cervus elaphus, n = 46), resulting in cross-species amplification rates of 94.5% and 89.1%, respectively. Based on polymorphic information content (>0.25) and genotyping fidelity, we selected 16 of these EST-SSRs for species identification. This marker set revealed significant genetic differentiation based on the fixation index and genetic distance values. Principal coordinate analysis and STRUCTURE analysis revealed distinct clusters of species and clearly identified red-sika hybrids. These markers showed applicability across different genera and proved suitable for identification and phylogenetic analyses across deer species.
Subjects
MICROSATELLITE MARKERS; MITOCHONDRIAL-DNA; CERVUS-NIPPON; VELVET ANTLER; C-ELAPHUS; TRANSCRIPTOME; SOFTWARE; CERVIDAE; INTROGRESSION; HYBRIDIZATION
SDGs

[SDGs]SDG15

Publisher
PUBLIC LIBRARY SCIENCE
Type
journal article

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