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Target-site basis for resistance to imazethapyr in redroot amaranth (Amaranthus retroflexus L.)

机译:红red菜(Amaranthus retroflexus L.)对咪唑乙烟的抗性的靶位基础

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Experiments were conducted to confirm imazethapyr resistance in redroot amaranth (Amaranthus retroflexus L.) and study the target-site based mechanism for the resistance. Whole-plant response experiments revealed that the resistant (R) population exhibited 19.16 fold resistance to imazethapyr compared with the susceptible (S) population. In vitro ALS activity assay demonstrated that the imazethapyr I-50 value of the R population was 21.33 times greater than that of the S population. However, qRT-PCR analysis revealed that there is no difference in ALS gene expression between the R and S populations. Sequence analysis revealed an Asp-376-Glu substitution in ALS in the R population. In order to verify that the imazethapyr resistance was conferred by Asp-376-Glu mutation, the ALS-R and ALS-S genes were fused to the CaMV 35S promoter and introduced into Arabidopsis respectively. The expression of ALS-R in transgenic Arabidopsis plants exhibited 13.79 fold resistance to imazethapyr compared to ALS-S transgenic Arabidopsis. (C) 2015 Elsevier Inc. All rights reserved.
机译:进行实验以确认红根a菜(Amaranthus retroflexus L.)中的咪唑乙烟抗性,并研究基于靶位的抗性机理。全植物响应实验表明,与易感(S)群体相比,抗性(R)群体对咪唑乙烟的耐药性高19.16倍。体外ALS活性测定表明,R种群的咪唑乙烟碱I-50值是S种群的21.33倍。但是,qRT-PCR分析显示R和S种群之间的ALS基因表达没有差异。序列分析揭示了R群体中ALS中的Asp-376-Glu取代。为了验证通过Asp-376-Glu突变赋予了咪唑乙草胺抗性,将ALS-R和ALS-S基因融合到CaMV 35S启动子上并分别引入拟南芥中。与ALS-S转基因拟南芥相比,转基因拟南芥植物中ALS-R的表达对咪唑乙烟具有13.79倍的抗性。 (C)2015 Elsevier Inc.保留所有权利。

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