首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Two Novel er1 Alleles Conferring Powdery Mildew (Erysiphe pisi) Resistance Identified in a Worldwide Collection of Pea (Pisum sativum L.) Germplasms
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Two Novel er1 Alleles Conferring Powdery Mildew (Erysiphe pisi) Resistance Identified in a Worldwide Collection of Pea (Pisum sativum L.) Germplasms

机译:在世界范围内的豌豆(Pisum sativum L.)种质资源中鉴定出两个赋予白粉病(Erysiphe pisi)抗性的新型er1等位基因。

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摘要

Powdery mildew caused by DC. severely affects pea crops worldwide. The use of resistant cultivars containing the gene is the most effective way to control this disease. The objectives of this study were to reveal alleles contained in 55 -resistant pea germplasms and to develop the functional markers of novel alleles. Sequences of 10 homologous cDNA clones from each germplasm accession were used to determine their alleles. The frame shift mutations and various alternative splicing patterns were observed during transcription of the gene. Two novel alleles, -8 and -9, were discovered in the germplasm accessions G0004839 and G0004400, respectively, and four known alleles were identified in 53 other accessions. One mutation in G0004839 was characterized by a 3-bp (GTG) deletion of the wild-type cDNA, resulting in a missing valine at position 447 of the PsMLO1 protein sequence. Another mutation in G0004400 was caused by a 1-bp (T) deletion of the wild-type cDNA sequence, resulting in a serine to leucine change of the PsMLO1 protein sequence. The -8 and -9 alleles were verified using resistance inheritance analysis and genetic mapping with respectively derived F and F populations. Finally, co-dominant functional markers specific to -8 and -9 were developed and validated in populations and pea germplasms. These results improve our understanding of resistance in pea germplasms worldwide and provide powerful tools for marker-assisted selection in pea breeding.
机译:DC引起的白粉病。严重影响了全世界的豌豆作物。使用含有该基因的抗性品种是控制这种疾病的最有效方法。这项研究的目的是揭示55个抗性豌豆种质中包含的等位基因,并开发新型等位基因的功能标记。来自每个种质材料的10个同源cDNA克隆的序列用于确定其等位基因。在基因转录过程中观察到了移码突变和各种可变的剪接模式。在种质登录号G0004839和G0004400中分别发现了两个新的等位基因-8和-9,在其他53个登录号中鉴定了四个已知的等位基因。 G0004839中的一个突变的特征在于野生型cDNA的3 bp(GTG)缺失,导致PsMLO1蛋白序列第447位的缬氨酸缺失。 G0004400中的另一个突变是由野生型cDNA序列的1 bp(T)缺失引起的,导致PsMLO1蛋白序列从丝氨酸变为亮氨酸。使用抗性遗传分析和分别针对F和F群体的遗传图谱验证了-8和-9等位基因。最后,在种群和豌豆种质中开发并验证了特异于-8和-9的共性功能标记。这些结果增进了我们对全世界豌豆种质抗性的了解,并为豌豆育种中标记辅助选择提供了有力的工具。

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