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首页> 外文期刊>Molecular Biotechnology >Silicon Carbide Whisker-Mediated Embryogenic Callus Transformation of Cotton (Gossypium hirsutum L.) and Regeneration of Salt Tolerant Plants
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Silicon Carbide Whisker-Mediated Embryogenic Callus Transformation of Cotton (Gossypium hirsutum L.) and Regeneration of Salt Tolerant Plants

机译:碳化硅晶须介导的棉花(Gossypium hirsutum L.)胚发生愈伤组织转化和耐盐植物的再生

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摘要

A silicon carbide whisker-mediated gene transfer system with recovery of fertile and stable transformants was developed for cotton (Gossypium hirsutum L.) cv. Coker-312. Two-month-old hypocotyl-derived embryogenicon-embryogenic calli at different days after subculture were treated with silicon carbide whiskers for 2 min in order to deliver pGreen0029 encoding GUS gene and pRG229 AVP1 gene, encoding Arabidopsis vacuolar pyrophosphatase, having neomycin phosphotransferaseII (nptII) genes as plant-selectable markers. Three crucial transformation parameters, i.e., callus type, days after subculture and selection marker concentration for transformation of cotton calli were evaluated for optimum efficiency of cotton embryogenic callus transformation giving upto 94% transformation efficiency. Within six weeks, emergence of kanamycin-resistant (kmr) callus colonies was noted on selection medium. GUS and Southern blot analysis showed expression of intact and multiple transgene copies in the transformed tissues. Kanamycin wiping of leaves from T1, T2, and T3 progeny plants revealed that transgenes were inherited in a Mendelian fashion. Salt treatment of T1 AVP1 transgenic cotton plants showed significant enhancement in salt tolerance as compared to control plants. Thus far, this is first viable physical procedure after particle bombardment available for cotton that successfully can be used to generate fertile cotton transformants.
机译:为棉花(Gossypium hirsutum L.)cv开发了具有可育和稳定转化体回收能力的碳化硅晶须介导的基因转移系统。 Coker-312。将继代培养后不同天数的两个月大的下胚轴衍生的胚性/非胚性愈伤组织用碳化硅晶须处理2分钟,以便递送编码GUS基因的pGreen0029和编码拟南芥液泡焦磷酸酶的pRG229 AVP1基因,并具有新霉素磷酸转移酶II( nptII)基因作为植物选择标记。评价了三个关键的转化参数,即愈伤组织类型,继代培养后的天数和用于转化棉花愈伤组织的选择标记物的浓度,以获得棉花胚发生愈伤组织转化的最佳效率,转化效率高达94%。在六周内,在选择培养基上发现了卡那霉素抗性(kmr )愈伤组织菌落的出现。 GUS和Southern印迹分析显示了完整和多个转基因拷贝在转化组织中的表达。用卡那霉素擦拭T1 ,T2 和T3 后代植物的叶子表明,转基因以孟德尔方式遗传。与对照植物相比,T1 AVP1转基因棉花植物的盐处理表现出显着的耐盐性增强。迄今为止,这是可用于棉花的粒子轰击之后的第一个可行的物理程序,该程序可成功用于产生可育的棉花转化体。

著录项

  • 来源
    《Molecular Biotechnology 》 |2008年第2期| 161-169| 共9页
  • 作者单位

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

    Plant Biotechnology Division National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    GUS; AVP1; nptII; Embryogenicon-embryogenic; Whiskers; Transformation;

    机译:GUS;AVP1;nptII;胚性/非胚性;晶须;转化;

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