Hu Shiyuan, Luo Kai, Tang Tao, Ma Guolan, Peng Yajun, Zhang Yuzhu, Liu Yang, Pan Lang, Li Sifu
College of Plant Protection, Hunan Agricultural University, Changsha 410128, China.
Institute of Plant Protection, Hunan Academy of Agricultural Sciences, Changsha 410125, China.
Plants (Basel). 2025 Feb 1;14(3):425. doi: 10.3390/plants14030425.
Mutagenesis breeding, combined with the application of corresponding herbicides to develop herbicide-resistant rice germplasm, provides great promise for the management of weeds and weedy rice. In this study, a topramezone-resistant rice mutant, TZR1, was developed from the indica rice line Chuangyu 9H (CY9H) through radiation mutagenesis and topramezone selection. Dose-response curves revealed that the resistance index of TZR1 to topramezone was 1.94-fold compared to that of CY9H. The resistance mechanism of TZR1 was not due to target-site resistance. This resistance could be reversed by a specific inhibitor of glutathione -transferase (GST). The activity of antioxidant enzymes was analyzed. SNPs and Indels were detected using whole-genome resequencing; differentially expressed genes were identified through RNA sequencing. Then, they underwent Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses. Key candidate genes associated with topramezone resistance were validated via a real-time quantitative PCR assay. Five GST genes, two UDP-glycosyltransferase genes, and three ATP-binding cassette transporter genes were identified as potential contributors to topramezone detoxification in TZR1. Overall, these findings suggest that GST enzymes possibly play an important role in TZR1 resistance to topramezone. This study will provide valuable information for the scientific application of 4-hydroxyphenylpyruvate dioxygenase inhibitors in paddy fields in future.
诱变育种,结合应用相应除草剂来培育抗除草剂水稻种质,为杂草和杂草稻的治理带来了巨大希望。在本研究中,通过辐射诱变和甲基磺草酮筛选,从籼稻品种创育9H(CY9H)培育出了一个抗甲基磺草酮的水稻突变体TZR1。剂量反应曲线显示,TZR1对甲基磺草酮的抗性指数是CY9H的1.94倍。TZR1的抗性机制并非源于靶标位点抗性。这种抗性可被谷胱甘肽-S-转移酶(GST)的特异性抑制剂逆转。分析了抗氧化酶的活性。利用全基因组重测序检测单核苷酸多态性(SNP)和插入缺失(Indel);通过RNA测序鉴定差异表达基因。然后,对它们进行基因本体论(Gene Ontology)和京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes)富集分析。通过实时定量PCR分析验证了与甲基磺草酮抗性相关的关键候选基因。五个GST基因、两个尿苷二磷酸糖基转移酶基因和三个ATP结合盒转运蛋白基因被确定为TZR1中甲基磺草酮解毒的潜在贡献者。总体而言,这些发现表明GST酶可能在TZR1对甲基磺草酮的抗性中发挥重要作用。本研究将为未来4-羟基苯丙酮酸双加氧酶抑制剂在稻田中的科学应用提供有价值的信息。