Huang Zhaofeng, Chen Jinyi, Zhang Chaoxian, Huang Hongjuan, Wei Shouhui, Zhou Xinxin, Chen Jingchao, Wang Xu
Key Laboratory of Weed and Rodent Biology and Management, Institute of Plant Protection (IPP), Chinese Academy of Agricultural Sciences (CAAS), China.
Key Laboratory of Weed and Rodent Biology and Management, Institute of Plant Protection (IPP), Chinese Academy of Agricultural Sciences (CAAS), China.
Pestic Biochem Physiol. 2016 Mar;128:10-5. doi: 10.1016/j.pestbp.2015.10.011. Epub 2015 Oct 20.
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 I50 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.
开展了实验以确认红根苋(反枝苋)对咪唑乙烟酸的抗性,并研究基于靶标的抗性机制。整株反应实验表明,抗性(R)种群对咪唑乙烟酸的抗性是敏感(S)种群的19.16倍。体外乙酰乳酸合成酶(ALS)活性测定表明,R种群的咪唑乙烟酸I50值比S种群高21.33倍。然而,定量逆转录聚合酶链反应(qRT-PCR)分析显示,R种群和S种群之间ALS基因表达没有差异。序列分析显示,R种群的ALS中存在天冬氨酸-376-谷氨酸替换。为了验证咪唑乙烟酸抗性是由天冬氨酸-376-谷氨酸突变赋予的,将ALS-R和ALS-S基因分别与花椰菜花叶病毒(CaMV)35S启动子融合,并导入拟南芥。与ALS-S转基因拟南芥相比,转基因拟南芥植株中ALS-R的表达对咪唑乙烟酸表现出13.79倍的抗性。