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基于SSR分子标记的青稞品种鉴定及遗传多样性分析OA

SSR Marker Based Analysis for Identification and Genetic Diversity of Hulless Barley Varieties

中文摘要英文摘要

为了筛选一套适合中国青稞品种鉴定标准的SSR核心引物,并建立青稞品种分子鉴定体系和DNA指纹数据库,基于国内外已报道的青稞SSR标记,对155个青稞品种进行PCR扩增和标记筛选验证,并分析其遗传多样性和鉴别效率.结果表明,从200对SSR引物中,筛选出峰型简单易读取、多态性好、扩增稳定性高、染色体上分布均匀的核心引物21对,用云青4号、迪青4号、昆仑8号等31个参照品种验证了 21对核心引物的稳定性和可靠性.利用21对核心引物构建了 155个青稞品种的指纹数据库,并检测到137个等位变异,每对引物等位变异的范围为2~10个,平均值为6.52个;PIC值范围为0.39~0.85,平均值为0.68,高多态性位点占比95.24%;21对核心引物可区分155个品种中的153个品种,引物鉴别效率为99.991%.通过聚类分析、群体结构分析和主成分分析,将154个青稞品种分为3个类群,品种间遗传多样性丰富,45.81%的品种遗传背景简单.由此可见,基于SSR分子标记建立的青稞品种鉴定体系鉴定效果好,应用性强,可用于青稞品种真实性鉴定、辅助DUS测试近似品种筛选、新品种权保护等领域;155个青稞品种的DNA指纹数据库和遗传多样性分析结果可为未来青稞育种提供一定参考.

To establish a molecular identification system and DNA fingerprint database for hulless bar-ley(Hordeum vulgare L.var.nudum Hook.f.)varieties in China,this study aimed to screen a set of SSR core primers suitable for national variety identification standards,thereby providing technical support for variety authentication,management,and new variety protection.Based on previously re-ported SSR markers of hulless barley,PCR amplification,marker screening,and validation were per-formed across diverse varieties,followed by analyses of genetic diversity and discrimination efficiency.Using 155 hulless barley accessions,200 SSR primer pairs were subjected to polymorphism screening.Twenty-one core primers were selected based on criteria including clear and easily interpretable peak patterns,high polymorphism(mean PIC=0.68),amplification stability,and even chromosomal dis-tribution.Reference varieties(e.g.,Yunqing 4,Diqing 4,and Kunlun 8)were employed to validate the stability and reliability of these primers.The constructed DNA fingerprint database for 155 acces-sions detected 137 alleles,ranging from 2 to 10 per locus(mean=6.52).The polymorphism informa-tion content(PIC)values varied between 0.39 and 0.85(mean=0.68),with 95.24%of loci classified as highly polymorphic(PIC>0.5).These 21 primers achieved a discrimination efficiency of 99.991%,distinguishing 153 out of 155 accessions.Cluster analysis,population structure analysis,and principal component analysis classified the 154 accessions into three distinct groups,revealing rich genetic di-versity and simple genetic backgrounds in 45.81%of the accessions.The SSR-based identification system developed in this study demonstrated high accuracy and practical applicability,enabling au-thenticity verification,auxiliary screening of approximate varieties in DUS testing,and intellectual property protection.Furthermore,the DNA fingerprint database and genetic diversity analysis pro-vide valuable molecular-level insights for future hulless barley breeding programs.

滕彩玲;杨晓洪;荆若男;张凯淅;法永英;赵春芳;韩瑞玺;刘艳芳

云南省农业科学院质量标准与检测技术研究所,云南 昆明 650205||农业农村部植物新品种测试(昆明)分中心,云南 昆明 650205云南省农业科学院质量标准与检测技术研究所,云南 昆明 650205||农业农村部植物新品种测试(昆明)分中心,云南 昆明 650205农业农村部科技发展中心,北京 100176农业农村部科技发展中心,北京 100176云南省农业科学院质量标准与检测技术研究所,云南 昆明 650205||农业农村部植物新品种测试(昆明)分中心,云南 昆明 650205昭通学院农学与生命科学学院,云南昭通 657000农业农村部科技发展中心,北京 100176云南省农业科学院质量标准与检测技术研究所,云南 昆明 650205||农业农村部植物新品种测试(昆明)分中心,云南 昆明 650205

农业科技

青稞SSR标记品种鉴定遗传多样性

Hulless barleySSR markersVariety identificationGenetic diversity

《麦类作物学报》 2026 (6)

754-767,14

科技部生物育成品种DUS测试工具装备研发项目(2023ZD0406106)云南省重大科技专项(202502AE090022)云南省重点研发计划项目(202503AP140031)云南省农业科学院预研项目中国科学技术部国际杰青计划项目(国科外[2025]28号)

10.7606/j.issn.1009-1041.2026.06.06

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