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Targeted and Untargeted Approaches Unravel Novel Candidate Genes and Diagnostic SNPs for Quantitative Resistance of the Potato (Solanum tuberosum L.) to Phytophthora infestans Causing the Late Blight Disease

机译:有针对性和非针对性的方法揭示了新的候选基因和诊断性SNPs对马铃薯(Solanum tuberosum L.)对疫病疫霉的致病性定量抗性

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摘要

The oomycete Phytophthora infestans causes late blight of potato, which can completely destroy the crop. Therefore, for the past 160 years, late blight has been the most important potato disease worldwide. The identification of cultivars with high and durable field resistance to P. infestans is an objective of most potato breeding programs. This type of resistance is polygenic and therefore quantitative. Its evaluation requires multi-year and location trials. Furthermore, quantitative resistance to late blight correlates with late plant maturity, a negative agricultural trait. Knowledge of the molecular genetic basis of quantitative resistance to late blight not compromised by late maturity is very limited. It is however essential for developing diagnostic DNA markers that facilitate the efficient combination of superior resistance alleles in improved cultivars. We used association genetics in a population of 184 tetraploid potato cultivars in order to identify single nucleotide polymorphisms (SNPs) that are associated with maturity corrected resistance (MCR) to late blight. The population was genotyped for almost 9000 SNPs from three different sources. The first source was candidate genes specifically selected for their function in the jasmonate pathway. The second source was novel candidate genes selected based on comparative transcript profiling (RNA-Seq) of groups of genotypes with contrasting levels of quantitative resistance to P. infestans. The third source was the first generation 8.3k SolCAP SNP genotyping array available in potato for genome wide association studies (GWAS). Twenty seven SNPs from all three sources showed robust association with MCR. Some of those were located in genes that are strong candidates for directly controlling quantitative resistance, based on functional annotation. Most important were: a lipoxygenase (jasmonate pathway), a 3-hydroxy-3-methylglutaryl coenzyme A reductase (mevalonate pathway), a P450 protein (terpene biosynthesis), a transcription factor and a homolog of a major gene for resistance to P. infestans from the wild potato species Solanum venturii. The candidate gene approach and GWAS complemented each other as they identified different genes. The results of this study provide new insight in the molecular genetic basis of quantitative resistance in potato and a toolbox of diagnostic SNP markers for breeding applications.
机译:卵菌疫霉菌感染导致马铃薯晚疫病,这可能完全破坏作物。因此,在过去的160年中,晚疫病已成为全世界最重要的马铃薯疾病。大多数马铃薯育种计划的目标是鉴定对病原菌具有高而持久的田间抗性的品种。这种类型的抗性是多基因的,因此是定量的。其评估需要多年和位置试验。此外,对晚疫病的定量抗性与晚熟植物相关,这是不利的农业特性。对晚疫病抗性定量分析的分子遗传学基础知识并未受到后期成熟性的损害。然而,对于开发诊断性DNA标记至关重要,该标记可促进优良抗性等位基因在改良品种中的有效结合。我们使用了184个四倍体马铃薯品种种群的关联遗传学,以鉴定与成熟抗晚疫病的抗性(MCR)相关的单核苷酸多态性(SNP)。对来自三个不同来源的近9000个SNP进行了基因分型。第一个来源是针对其在茉莉酸酯途径中的功能而专门选择的候选基因。第二个来源是基于基因型组的比较转录谱分析(RNA-Seq)选择的新型候选基因,其对致病疫霉的定量抗性水平相反。第三个来源是马铃薯中可用于基因组范围关联研究(GWAS)的第一代8.3k SolCAP SNP基因分型阵列。来自所有三个来源的27个SNP显示与MCR密切相关。其中一些位于基于功能注释而直接控制定量抗性的强候选基因中。最重要的是:脂氧合酶(茉莉酸途径),3-羟基-3-甲基戊二酰辅酶A还原酶(甲羟戊酸途径),P450蛋白(萜烯生物合成),转录因子和对P抗性的主要基因的同源物。野生马铃薯物种文氏茄(Solanum venturii)的感染。候选基因方法与GWAS互补,因为它们鉴定了不同的基因。这项研究的结果为马铃薯定量抗性的分子遗传基础和用于育种应用的诊断性SNP标记工具箱提供了新的见识。

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