首页> 外文期刊>Archives of Insect Biochemistry and Physiology >GENETIC TRANSFORMATION MEDIATED BY piggyBac IN THE ASIAN CORN BORER, Ostrinia furnacalis (LEPIDOPTERA: CRAMBIDAE)
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GENETIC TRANSFORMATION MEDIATED BY piggyBac IN THE ASIAN CORN BORER, Ostrinia furnacalis (LEPIDOPTERA: CRAMBIDAE)

机译:由piggyBac介导的亚洲玉米(Ostrinia furnacalis)的遗传转化(LEPIDOPTERA:CRAMBIDAE)

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摘要

The Asiancorn borer, Ostrinia furnacalis, is a serious pest of corn, sorghum, and cotton in China and other Asian countries. The present study is the first attempt to establish the transgenic line in O. furnacalis using a piggyBac transposon, which will shed light on the future genetic control of O. furnacalis. A piggyBac vector pBac[A3EGFP] was constructed to express enhanced green fluorescence protein (EGFP)under the control of Bombyx mori actin3 promoter. Transient EGFP expression was detected 48 h after preblastodermic microinjection of pBac[A3EGFP] and the excision assay showed the transgenic vector was precisely excised. In G1 animals, PCR (polymerase chain reaction)-based investigations revealed that the exogenous gene had been introduced into O. furnacalis genome and expressed at the transcriptional level. Western blot analysis showed EGFP expression at the protein level, indicating the heritability of the transgene.
机译:亚洲玉米bore,Ostrinia furnacalis,是中国和其他亚洲国家的玉米,高粱和棉花的严重害虫。本研究是使用piggyBac转座子在弗氏杯中建立转基因品系的首次尝试,这将为弗氏杯的未来遗传控制提供启示。构建了一个piggyBac载体pBac [A3EGFP],以在家蚕肌动蛋白3启动子的控制下表达增强的绿色荧光蛋白(EGFP)。胚泡显微注射pBac [A3EGFP]后48小时,检测到瞬时EGFP表达,并且切除分析表明已正确切除了转基因载体。在G1动物中,基于PCR(聚合酶链反应)的研究表明,外源基因已被引入呋喃卡因州的基因组中并在转录水平表达。蛋白质印迹分析显示EGFP在蛋白水平表达,表明转基因的遗传性。

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