首页> 美国卫生研究院文献>PLoS Clinical Trials >Genome Re-Sequencing and Functional Analysis Places the Phytophthora sojae Avirulence Genes Avr1c and Avr1a in a Tandem Repeat at a Single Locus
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Genome Re-Sequencing and Functional Analysis Places the Phytophthora sojae Avirulence Genes Avr1c and Avr1a in a Tandem Repeat at a Single Locus

机译:基因组重测序和功能分析在单个位点串联重复放置大豆疫霉无毒力基因Avr1c和Avr1a。

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摘要

The aim of this work was to map and identify the Phytophthora sojae Avr1c gene. Progeny from a cross of P. sojae strains ACR10×P7076 were tested for virulence on plants carrying Rps1c. Results indicate that avirulence segregates as a dominant trait. We mapped the Avr1c locus by performing whole genome re-sequencing of composite libraries created from pooled samples. Sequence reads from avirulent (Pool1) and virulent (Pool2) samples were aligned to the reference genome and single nucleotide polymorphisms (SNP) were identified for each pool. High quality SNPs were filtered to select for positions where SNP frequency was close to expected values for each pool. Only three SNP positions fit all requirements, and these occurred in close proximity. Additional DNA markers were developed and scored in the F2 progeny, producing a fine genetic map that places Avr1c within the Avr1a gene cluster. Transient expression of Avr1c or Avr1a triggers cell death on Rps1c plants, but Avr1c does not trigger cell death on Rps1a plants. Sequence comparisons show that the RXLR effector genes Avr1c and Avr1a are closely related paralogs. Gain of virulence on Rps1c in P. sojae strain P7076 is achieved by gene deletion, but in most other strains this is accomplished by gene silencing. This work provides practical tools for crop breeding and diagnostics, as the Rps1c gene is widely deployed in commercial soybean cultivars.
机译:这项工作的目的是定位和鉴定大豆疫霉Avr1c基因。测试来自大豆假单胞菌菌株ACR10×P7076的杂交后代在携带Rps1c的植物上的毒力。结果表明,无毒力是主要特征。我们通过对从合并样本中创建的复合文库进行全基因组重新测序来绘制Avr1c基因座。将无毒样品(Pool1)和有毒样品(Pool2)的序列读数与参考基因组进行比对,并为每个库鉴定了单核苷酸多态性(SNP)。过滤高质量的SNP,以选择SNP频率接近每个库的预期值的位置。只有三个SNP位置可以满足所有要求,并且这些位置非常接近。开发了其他DNA标记并在F2后代中进行了评分,从而产生了将Avr1c置于Avr1a基因簇内的精细遗传图谱。 Avr1c或Avr1a的瞬时表达会触发Rps1c植物上的细胞死亡,但Avr1c不会触发Rps1a植物上的细胞死亡。序列比较表明,RXLR效应基因Avr1c和Avr1a是密切相关的旁系同源物。大豆疫霉菌株P7076中Rps1c的毒力获得是通过基因缺失实现的,但在大多数其他菌株中,这是通过基因沉默来实现的。由于Rps1c基因已广泛部署在商业大豆品种中,这项工作为作物育种和诊断提供了实用工具。

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