期刊文献+

硬脂酸脱氢酶基因ghSAD-1倒位重复构建的棉花遗传转化(英文) 被引量:1

Cotton Transformation Based on Inverted Repeat Construct of stearoyl-ACP△9 desaturase Gene ghSAD-1
下载PDF
导出
摘要 以种子特异性表达的大豆凝集素基因启动子、终止子以及棉株体内硬脂酰 -ACP△ 9脱氢酶的基因 gh SAD-1进行倒位重复基因构建 ,以农杆菌介导法转化陆地棉品种 Coker3 1 5,获得了较高的转化频率。PCR、Southern杂交及种子内脂肪酸组分含量分析。结果表明 ,该倒位重复基因的表达及沉默效应在不同的转基因品系间存在差异 ,硬脂酸含量分别由对照的 2 %提高至 4%~3 8.2 % ,而棕榈酸含量则明显降低。高含硬脂酸的转基因品系可作为棉子油品质改良的基础材料 。 A partial inverted repeat based gene construct was produced and cloned into the pBI-Lectin binary vector, using the strong seed specific so ybean Lectin promoter and cotton stearyol-ACP△9 desaturase gene ghSAD-1. The cotton cultivar G.hirsutum cv. Coker315 was then transformed by the co nstruct through Agrobacterium mediated infection. A relatively high tr ansformation freque ncy was obtained. Further analysis by PCR, Southern blotting and fatty acid comp osition analysis demonstrated that the expression or silencing effectiveness of the transgene was not in the same level among various transgenic lines, where th e stearic acid content was increased from 2 percent of the control to a range of 4~38.2 percent. These materials are valuable for the further improvement of cu rrent cottonseed oil in the future.
出处 《棉花学报》 CSCD 北大核心 2001年第5期304-308,共5页 Cotton Science
基金 This program is supported by CottonResearch &Development Corporation Australia andChinese Scholarship Council. All the right reservedin Australia
关键词 棉花 遗传转化 硬脂酸 脱氢酶基因 ghSAD-1 倒位重复 cotton seed oil stearic acid gene silence inverted r epeats
  • 相关文献

参考文献3

  • 1Jan M K,Trends Plant Science,1999年,4卷,9期,340页
  • 2Waterhouse P M,Proc Nat Acad Sci USA,1998年,95卷,13959页
  • 3Liu Q,Plant Physiol,1996年,110卷,1435页

同被引文献14

  • 1孙涛,卢美光,简桂良,林凤.棉花NBS类抗病基因类似物的生物信息学分析[J].棉花学报,2005,17(3):182-183. 被引量:4
  • 2SANTAMARIA M,Thomson C J,Read N D,et al.The promoter of a basic PR1-like gene,AtPRB1,from Arabidopsis establishes an organ-specific expression pattern and responsiveness to ethylene and methyl jasmonate[J].Plant Molecular Biology,2001,47:641-652.
  • 3THURAU T,Kifle S,Jung C,et al.The promoter of the nematode resistance gene Hs1pro-1 activates a nematode-responsive and feeding site-specific gene ex pression in sugar beet (Beta vulgaris L.) and Arabidopsis thaliana[J].Plant Molecular Biology,2003,52:643-660.
  • 4SHAH J,Klessig D F.Identification of a salicylic acid-responsive element in the promoter of the tobacco pathogenesis-related beta-1,3-glucanase gene,PR-2d[J].Plant J,1996,10(6):1089-101.
  • 5LIU Y G,Mitsukawa N,Oosumi T,et al.Efficient isolation and mapping of Arabidopsis thaliana TDNA insert junctions by thermal asymmetric interlaced PCR[J].Plant J,1995,8:457-463.
  • 6JEFFERSON R A,Kavanagh T A,Bevan M W.GUS fusions beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants[J].EMBO J,1987,6:3901-3907.
  • 7BRADFORD M M.A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding[J].Anal Biochem,1976,72:248-254.
  • 8JUNG H W,Kim K D,Hwang B K.Identification of pathogen-responsive regions in the promoter of a pepper lipid transfer protein gene (CALTPI) and the en hanced resistance of the CALTPI transgenic Arabi dopsis against pathogen and environmental stresses[J].Planta,2005,221(3):361-73.
  • 9BUCHEL A S,Brederode F T,Bol J F,et al.Mutation of GT-1 binding sites in the Pr-1A promoter influences the level of inducible gene expression in vivo[J].Plant Mol Biol,1999,40:387-396.
  • 10YU D,Chen C,Chen Z.Evidence for an important role of WRKY DNA binding proteins in the regulation of NPR1 gene expression[J].Plant Cell,2001,13:1527-1540.

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部