Construction of transposon-mediated baculovirus vector and expression of green fluorescent protein in insect cells and larvae

被引:0
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作者
ZHU Ying and QI Yipeng .Institute of Virology
机构
关键词
HaNPV; transposon-shuttle vector; recombinant virus; green fluorescent protein;
D O I
暂无
中图分类号
Q963 [昆虫遗传学];
学科分类号
071007 ;
摘要
A transposon-shuttle vector Hanpvid was constructed by using wild-type genomic DNA from Heliothis armigera nuclear polyhedrosis virus (HaNPV). lt could replicate in E. coli cells as a large plasmid and remain infectious when being induced into insect cells.Hanpvid comprises HaNPV DNA and a transposon cassette which includes a miniF replicon, a kanamycin resistance gene (kan), lacZa and an attachment site for Tn7 (attTn7). Recombinant virus rHa-FaGP was obtained after transposition of a donor plasmid carrying green fluorescent protein gene (gfp) and polyhedrin gene (ocu) into attTn7.SDS-PAGE analysis shows that both gfp and ocu genes were highly expressed in Heliothis armigera cells. Green Hemolymphocytes can be seen under a fluorescent microscope 4 d after recombinant virus rHa-FaGP infected the third-instar larvae. The infected larvae show strong green fluorescence 6 d post infection.##属性不符
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页码:158 / 163
页数:6
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