| Literature DB >> 26969434 |
Zhaofeng Huang1, Jinyi Chen1, Chaoxian Zhang2, Hongjuan Huang1, Shouhui Wei1, Xinxin Zhou3, Jingchao Chen1, Xu Wang1.
Abstract
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.Entities:
Keywords: Acetolactate synthase (ALS); Arabidopsis; Herbicide resistance; Imazethapyr
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Year: 2015 PMID: 26969434 DOI: 10.1016/j.pestbp.2015.10.011
Source DB: PubMed Journal: Pestic Biochem Physiol ISSN: 0048-3575 Impact factor: 3.963