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Stable chloroplast transformation of immature scutella and inflorescences in wheat (Triticum aestivum L.)

机译:小麦(小麦)中未成熟黄cut和花序的稳定叶绿体转化

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摘要

Chloroplast transformation in wheat was achieved by bombardment of scutella from immature embryos and immature inflorescences, respectively. A wheat chloroplast site-specific expression vector, pBAGNRK, was constructed by placing an expression cassette containing neomycin phosphotransferase II (nptII) and green fluorescent protein (gfp) as selection and reporter genes, respectively, in the intergenic spacer between atpB and rbcL of wheat chloroplast genome. Integration of gfp gene in the plastome was identified by polymerase chain reaction (PCR) analysis and Southern blotting using gfp gene as a probe. Expression of GFP protein was examined by western blot. Three positive transformants were obtained and the Southern blot of partial fragment of atpB and rbcL (targeting site) probes verified that one of them was homoplasmic. Stable expression of GFP fluorescence was confirmed by confocal microscopy in the leaf tissues from T1 progeny seedlings. PCR analysis of gfp gene also confirmed the inheritance of transgene in the T1 progeny. These results strengthen the feasibility of wheat chloroplast transformation and also give a novel method for the introduction of important agronomic traits in wheat through chloroplast transformation.
机译:小麦叶绿体的转化是通过分别轰击未成熟胚和未成熟花序的黄cut来实现的。通过将分别包含新霉素磷酸转移酶II(nptII)和绿色荧光蛋白(gfp)作为选择基因和报告基因的表达盒置于小麦atpB和rbcL之间的基因间隔区中,构建小麦叶绿体位点特异性表达载体pBAGNRK。叶绿体基因组。通过聚合酶链反应(PCR)分析和以gfp基因为探针的Southern杂交鉴定了gfp基因在质体中的整合。通过蛋白质印迹检查GFP蛋白的表达。获得了三个阳性转化体,并且atpB和rbcL(靶向位点)探针的部分片段的Southern印迹证实其中之一是同质的。共聚焦显微镜证实了T 1 后代幼苗叶片组织中GFP荧光的稳定表达。 gfp基因的PCR分析也证实了转基因在T 1 后代中的遗传。这些结果加强了小麦叶绿体转化的可行性,也为通过叶绿体转化引入重要的农艺性状提供了新的方法。

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  • 来源
    《Acta Biochimica et Biophysica Sinica》 |2011年第4期|p.284-291|共8页
  • 作者

    Guangyuan He;

  • 作者单位

    , College of Life Science and Technology, Huazhong University of Science & Technology,;

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  • 正文语种 eng
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