Department of Agricultural Production, College of Agricultural and Environmental Sciences, Makerere University, P.O. Box 7062, Kampala, Uganda.
Regional Study Center for the Improvement of Drought Adaptation, Senegalese Institute for Agricultural Research, BP 3320, Thiès, Senegal.
Theor Appl Genet. 2023 Mar 10;136(3):35. doi: 10.1007/s00122-023-04259-4.
We identified markers associated with GRD resistance after screening an Africa-wide core collection across three seasons in Uganda Groundnut is cultivated in several African countries where it is a major source of food, feed and income. One of the major constraints to groundnut production in Africa is groundnut rosette disease (GRD), which is caused by a complex of three agents: groundnut rosette assistor luteovirus, groundnut rosette umbravirus and its satellite RNA. Despite several years of breeding for GRD resistance, the genetics of the disease is not fully understood. The objective of the current study was to use the African core collection to establish the level of genetic variation in their response to GRD, and to map genomic regions responsible for the observed resistance. The African groundnut core genotypes were screened across two GRD hotspot locations in Uganda (Nakabango and Serere) for 3 seasons. The Area Under Disease Progress Curve combined with 7523 high quality SNPs were analyzed to establish marker-trait associations (MTAs). Genome-Wide Association Studies based on Enriched Compressed Mixed Linear Model detected 32 MTAs at Nakabango: 21 on chromosome A04, 10 on B04 and 1 on B08. Two of the significant markers were localised on the exons of a putative TIR-NBS-LRR disease resistance gene on chromosome A04. Our results suggest the likely involvement of major genes in the resistance to GRD but will need to be further validated with more comprehensive phenotypic and genotypic datasets. The markers identified in the current study will be developed into routine assays and validated for future genomics-assisted selection for GRD resistance in groundnut.
我们在乌干达的三个季节中筛选了一个全非核心收集品系,鉴定出与 GRD 抗性相关的标记。
在几个非洲国家,落花生被种植,是食物、饲料和收入的主要来源之一。非洲落花生生产的主要限制因素之一是落花生卷叶病(GRD),它是由三种因子的复合体引起的:花生卷叶辅助 luteovirus、花生卷叶 umbravirus 及其卫星 RNA。尽管经过多年的 GRD 抗性选育,但该疾病的遗传学尚未完全了解。本研究的目的是利用非洲核心收集品系来确定其对 GRD 反应的遗传变异水平,并绘制负责观察到的抗性的基因组区域。非洲落花生核心基因型在乌干达的两个 GRD 热点地区(Nakabango 和 Serere)进行了三个季节的筛选。结合 7523 个高质量 SNPs 的疾病进展曲线下面积分析用于建立标记-性状关联(MTAs)。基于富集压缩混合线性模型的全基因组关联研究在 Nakabango 检测到 32 个 MTAs:A04 染色体上 21 个,B04 上 10 个,B08 上 1 个。两个显著标记定位于 A04 染色体上假定 TIR-NBS-LRR 疾病抗性基因的外显子上。我们的结果表明,主要基因可能参与了 GRD 的抗性,但需要用更全面的表型和基因型数据集进一步验证。本研究中鉴定的标记将被开发成常规检测方法,并在未来的落花生 GRD 抗性基因组辅助选择中进行验证。