Molecular Characterization of Resistance to Nicosulfuron in Setaria viridis

The green foxtail, (L.) P. Beauv. (Poales: Poaceae), is a troublesome and widespread grass weed in China. The acetolactate synthase (ALS)-inhibiting herbicide nicosulfuron has been intensively used to manage , and this has substantially increased the selection pressure. Here we confirmed a 35.8-fold...

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Published inInternational journal of molecular sciences Vol. 24; no. 8; p. 7105
Main Authors Cao, Yi, Lan, Yuning, Huang, Hongjuan, Wei, Shouhui, Li, Xiangju, Sun, Ying, Wang, Ruolin, Huang, Zhaofeng
Format Journal Article
LanguageEnglish
Published Switzerland MDPI 12.04.2023
MDPI AG
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Summary:The green foxtail, (L.) P. Beauv. (Poales: Poaceae), is a troublesome and widespread grass weed in China. The acetolactate synthase (ALS)-inhibiting herbicide nicosulfuron has been intensively used to manage , and this has substantially increased the selection pressure. Here we confirmed a 35.8-fold resistance to nicosulfuron in an population (R376 population) from China and characterized the resistance mechanism. Molecular analyses revealed an Asp-376-Glu mutation of the gene in the R376 population. The participation of metabolic resistance in the R376 population was proved by cytochrome P450 monooxygenases (P450) inhibitor pre-treatment and metabolism experiments. To further elucidate the mechanism of metabolic resistance, eighteen genes that could be related to the metabolism of nicosulfuron were obtained bythe RNA sequencing. The results of quantitative real-time PCR validation indicated that three ATP-binding cassette (ABC) transporters ( , , and ), four P450 ( , , , and ), and two UDP-glucosyltransferase (UGT) ( and ), and one glutathione S-transferases (GST) ( ) were the major candidates that contributed to metabolic nicosulfuron resistance in . However, the specific role of these ten genes in metabolic resistance requires more research. Collectively, gene mutations and enhanced metabolism may be responsible for the resistance of R376 to nicosulfuron.
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These authors contributed equally to this work.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms24087105