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Genome-wide development of genomic SSR markers, polymorphism analysis, and dosage-aware SSR fingerprinting in hexaploid Camellia Oleifera  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Genome-wide development of genomic SSR markers, polymorphism analysis, and dosage-aware SSR fingerprinting in hexaploid Camellia Oleifera

作者:Zhang, Chengcai[1] Lin, Ping[1] Yao, Xiaohua[1] Ren, Huadong[1] Wang, Kailiang[1]

第一作者:张成才

通信作者:Ren, HD[1];Wang, KL[1]

机构:[1]Chinese Acad Forestry, Res Inst Subtrop Forestry, State Key Lab Tree Genet & Breeding, Key Lab Tree Breeding Zhejiang Prov, Hangzhou 311400, Peoples R China

年份:2025

卷号:25

期号:1

外文期刊名:BMC PLANT BIOLOGY

收录:;Scopus(收录号:2-s2.0-105022750563);WOS:【SCI-EXPANDED(收录号:WOS:001622368900001)】;

基金:This research was funded by Zhejiang Science and Technology Major Program on Agricultural New Variety Breeding (2021C02070-2) and the Special Investigation on Basic Resources of Science and Technology (2019FY100801).

语种:英文

外文关键词:Oil-Camellia; Genetic diversity; Polymorphism; Fingerprint; Cultivar identification

摘要:Background Oil-Camellia is an important woody oil crop, and most cultivated cultivars are hexaploid. Unresolved kinship among major cultivars and the lack of reliable identification methods have hindered both the development of new cultivars and the deployment of elite ones. An important reason is the limited availability of molecular markers suitable for genetic analysis. Results Using five published oil-Camellia genomes, we surveyed genome-wide SSRs and found densities of one SSR per 4.22-4.67 kb across species. Based on the C. oleifera var. Nanyongensis reference genome, we designed 14,854 primer pairs and validated 132 new SSR markers. Genetic diversity and relationships among 44 hexaploid cultivars were assessed with a 30-marker subset, yielding 3-21 alleles per locus; polymorphism information content ranged from 0.07 to 0.91. Phylogenetic analyses using dosage-resolved SSR genotypes revealed the genetic relationships between 44 cultivars. We evaluated the discriminatory power of each marker and identified a minimal set (Coz09127 and Coz14197) that distinguishes all cultivars; using these two core markers, we constructed-for the first time-fingerprints for 44 hexaploid C. oleifera cultivars. Conclusions We surveyed SSR distribution in oil-Camellia genomes and developed 132 SSR markers. Using 30 loci, we characterized genetic diversity and relationships among 44 hexaploid cultivars, and identified a minimal two-marker set that distinguishes all tested cultivars, enabling construction of cultivar DA-SSR fingerprints. These results strengthen the genetic toolkit for polyploid C. oleifera and support reliable cultivar identification and deployment in breeding and production.

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