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In maize,co-expression of GAT and GR79-EPSPS provides high glyphosate resistance,along with low glyphosate residues 被引量:2

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摘要 Herbicide tolerance has been the dominant trait introduced during the global commercialization of genetically modified(GM)crops.Herbicide-tolerant crops,especially glyphosate-resistant crops,offer great advantages for weed management;however,despite these benefits,glyphosate-resistant maize(Zea mays L.)has not yet been commercially deployed in China.To develop a new bio-breeding resource for glyphosate-resistant maize,we introduced a codon-optimized glyphosate N-acetyltransferase gene,gat,and the enolpyruvyl-shikimate-3-phosphate synthase gene,gr79-epsps,into the maize variety B104.We selected a genetically stable high glyphosate resistance(GR)transgenic event,designated GG2,from the transgenic maize population through screening with high doses of glyphosate.A molecular analysis demonstrated that single copy of gat and gr79-epsps were integrated into the maize genome,and these two genes were stably transcribed and translated.Field trials showed that the transgenic event GG2 could tolerate 9000 g acid equivalent(a.e.)glyphosate per ha with no effect on phenotype or yield.A gas chromatography-mass spectrometry(GC–MS)analysis revealed that,shortly after glyphosate application,the glyphosate(PMG)and aminomethylphosphonic acid(AMPA)residues in GG2 leaves decreased by more than 90%compared to their levels in HGK60 transgenic plants,which only harbored the epsps gene.Additionally,PMG and its metabolic residues(AMPA and N-acetyl-PMG)were not detected in the silage or seeds of GG2,even when far more than the recommended agricultural dose of glyphosate was applied.The co-expression of gat and gr79-epsps,therefore,confers GG2 with high GR and a low risk of herbicide residue accumulation,making this germplasm a valuable GR event in herbicide-tolerant maize breeding.
出处 《aBIOTECH》 EI CAS CSCD 2023年第4期277-290,共14页 生物技术通报(英文版)
基金 supported by the National Transgenic Major Program of China(2016ZX08003001),。
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  • 1李香菊,王贵启,李秉华,Blackshaw R E.麦秸覆盖与除草剂相结合对免耕玉米田杂草的控制效果研究[J].华北农学报,2003,18(F09):99-102. 被引量:45
  • 2唐洪元,王学鹗.中国北纬34—35度农田主要杂草经相分布和危害[J].杂草学报(内刊),1989,3(1):1-8. 被引量:4
  • 3李香菊,杨殿贤,赵郁强,李咏军.除草剂对作物产生药害的原因及治理对策[J].农药科学与管理,2007,28(3):39-44. 被引量:31
  • 4Padgette S R, Re D B, Gasser C S, Eichholtz D A, Frazier R B, Hironaka C M, Levine E B, Sha D M, Fraley R T, Kishore G M. 1991. Site-directed mutagenesis of a conserved region of the 5-enolpyruvylshikimate-3-phosphate synthase active site. The Journal of Biological Chemistry, 266, 22364-22369.
  • 5Schledzewski K, Mendel R. 1994. Quantitative transient gene expression: comparison of the promoters for maize polyubiquitin 1 rice actin 1, maize derivedEmu and CaMV 35S in cells of barley, maize and tobacco. Transgenic Research, 3, 249-255.
  • 6Schmid J, Amrhein N. 1995. Molecular organization of the shikimate pathway in higher plants. Phytoehemistry, 39, 737- 749.
  • 7Xu X, Kawasaki S, Fujimura T, Wang C. 2005. A protocol for high-throughput extraction of DNA from rice leaves. Plant Molecular Biology Reporter, 23, 291-295.
  • 8Zhou M, Xu H L, Wei X L, Ye Z Q, Wei L P, Gong W M, Wang Y Q, Zhu Z. 2006. Identification of a glyphosate-resistant mutant of rice 5-enolpyruvylshikimate-3-phosphate synthase using a directed evolution strategy. Plant Physiology, 140, 184-195.
  • 9Battraw M J, Hall T C. 1990. Histochemical analysis of CaMV 35S promoter-β-glucuronidase gene expression in transgenic rice plants. Plant Molecular Biology, 15, 527-538.
  • 10Cao M X, Huang J Q, Wei Z M, Yao Q H, Wan C Z, Lu J A. 2004. Engineering higher yield and herbicide resistance in rice by agrobacterium-mediated multiple gene transformation. Crop Science, 44, 2206-2213.

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