Rana Kusum, Atri Chhaya, Akhatar Javed, Kaur Rimaljeet, Goyal Anna, Singh Mohini Prabha, Kumar Nitin, Sharma Anju, Sandhu Prabhjodh S, Kaur Gurpreet, Barbetti Martin J, Banga Surinder S
School of Agricultural Biotechnology, Punjab Agricultural University, Ludhiana, India.
Department of Plant Breeding and Genetics, Punjab Agricultural University, Ludhiana, India.
Front Plant Sci. 2019 Aug 6;10:1015. doi: 10.3389/fpls.2019.01015. eCollection 2019.
A set of 96 - introgression lines (ILs) were developed with genomic regions associated with stem rot () resistance from a wild species . ILs were assessed for their resistance responses to stem inoculation with , over three crop seasons (season I, 2011/2012; II, 2014/2015; III, 2016-2017). Initially, ILs were genotyped with transferable SSR markers and subsequently through genotyping by sequencing. SSR based association mapping identified six marker loci associated to resistance in both A and B genomes. Subsequent genome-wide association analysis (GWAS) of 84 ILs recognized a large number of SNPs associated to resistance, in chromosomes A03, A06, and B03. Chromosomes A03 and A06 harbored the maximum number of resistance related SNPs. Annotation of linked genomic regions highlighted an array of resistance mechanisms in terms of signal transduction pathways, hypersensitive responses and production of anti-fungal proteins and metabolites. Of major importance was the clustering of SNPs, encoding multiple resistance genes on small regions spanning approximately 885 kb region on chromosome A03 and 74 kb on B03. Five SNPs on chromosome A03 (6,390,210-381) were associated with LRR-RLK (receptor like kinases) genes that encode LRR-protein kinase family proteins. Genetic factors associated with pathogen-associated molecular patterns (PAMPs) and effector-triggered immunity (ETI) were predicted on chromosome A03, exhibiting 11 SNPs (6,274,763-994). These belonged to three R-Genes encoding TIR-NBS-LRR proteins. Marker trait associations (MTAs) identified will facilitate marker assisted introgression of these critical resistances, into new cultivars of initially and, subsequently, into other crop species.
利用来自野生种的与茎腐病抗性相关的基因组区域,培育了一组96个渗入系(ILs)。在三个作物季(第一季,2011/2012年;第二季,2014/2015年;第三季,2016 - 2017年),对这些渗入系进行了茎接种病原菌后的抗性反应评估。最初,利用可转移的SSR标记对渗入系进行基因分型,随后通过测序进行基因分型。基于SSR的关联作图在A和B基因组中均鉴定出6个与抗性相关的标记位点。随后对84个渗入系进行全基因组关联分析(GWAS),在A03、A06和B03染色体上识别出大量与抗性相关的单核苷酸多态性(SNP)。A03和A06染色体上抗性相关SNP的数量最多。对连锁基因组区域的注释突出了一系列抗性机制,涉及信号转导途径、过敏反应以及抗真菌蛋白和代谢物的产生。最重要的是,SNP在小区域内聚集,在A03染色体上约885 kb区域和B03染色体上74 kb区域编码多个抗性基因。A03染色体上的5个SNP(6,390,210 - 381)与编码LRR蛋白激酶家族蛋白的LRR - RLK(类受体激酶)基因相关。在A03染色体上预测到与病原体相关分子模式(PAMPs)和效应子触发免疫(ETI)相关的遗传因子,表现出11个SNP(6,274,763 - 994)。这些属于三个编码TIR - NBS - LRR蛋白的R基因。所鉴定的标记 - 性状关联(MTAs)将有助于将这些关键抗性通过标记辅助渗入到最初的新品种中,随后再渗入到其他作物品种中。