Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo, Colombo, Sri Lanka.
Department of Biotechnology, Faculty of Agriculture and Plantation Management, Wayamba University of Sri Lanka, Kuliyapitiya, Sri Lanka.
Plant Cell Rep. 2021 Feb;40(2):351-359. doi: 10.1007/s00299-020-02637-6. Epub 2020 Nov 27.
Identification of an EST-SSR molecular marker associated with Blister blight, a common fungal disease of tea, facilitating marker-assisted selection, marking a milestone in tea molecular breeding. lister blight (BB) leaf disease of tea, caused by the fungus Exobasidium vexans, results in 25-30% crop loss annually. BB is presently controlled by Cu based fungicides, but genetic resistance is the most viable option in disease management. Tea is a naturally out-crossing, woody perennial necessitating a long time for completion of a breeding programme. Marker-assisted selection (MAS) is vital to expedite breeding programmes and also for better accuracy in gene identification. The aim of the current research was to derive marker-trait associations using an F population segregating for BB. The population was genotyped at 11 expressed sequence tag simple sequence repeat loci followed by detecting the alleles by fragment analysis. The genotypic and phenotypic data were subjected to single-marker analysis resulting in the identification of EST-SSR073 as a diagnostic marker amplifying three alleles of the sizes, 168, 170 and 190 bp in F. Of them, alleles 190 and 168 bp were confirmed to concur BB resistance and susceptibility, respectively. The alleles were validated in a panel of 64 tea cultivars, resulting in the amplification of 12 alleles at EST-SSR073. The EST-SSR073 allele sequences matched with Camellia sinensis photosystem-I reaction center subunit-II. The marker EST-SSR073 can be effectively used in breeding tea against BB, recording a milestone in MAS in tea.
茶疱病(BB)是由外生囊菌(Exobasidium vexans)引起的茶树叶片病害,每年导致 25-30%的作物损失。目前,BB 是通过铜基杀菌剂来控制,但遗传抗性是疾病管理中最可行的选择。茶树是一种天然异交的木本多年生植物,完成一个育种计划需要很长时间。标记辅助选择(MAS)对于加速育种计划和提高基因鉴定的准确性至关重要。本研究旨在利用一个对 BB 进行分离的 F 群体,从 EST-SSR 中获得标记与性状的关联。该群体在 11 个表达序列标签简单重复序列(EST-SSR)位点进行了基因型分析,随后通过片段分析检测了等位基因。对基因型和表型数据进行单标记分析,鉴定出 EST-SSR073 是一个可扩增 168、170 和 190 bp 三个等位基因的诊断标记。其中,等位基因 190 和 168 bp 被证实分别与 BB 抗性和敏感性相关。该等位基因在 64 个茶树品种的面板中进行了验证,在 EST-SSR073 上扩增出 12 个等位基因。EST-SSR073 等位基因序列与茶树光系统-I 反应中心亚基-II 相匹配。该标记 EST-SSR073 可有效地用于茶树抗 BB 的育种,在茶树 MAS 中记录了一个里程碑。