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作 者:邱亚峰[1] 葛菲菲[1] 张雪莲[1] 陈溥言[1]
机构地区:[1]南京农业大学动物疫病诊断与免疫重点实验室,南京210095
出 处:《中国生物工程杂志》2006年第5期11-16,共6页China Biotechnology
基 金:国家"863"计划资助项目(2002AA245051)
摘 要:利用Primerprimer5.0软件设计两条引物,将loxP位点分别引入正、反向引物,以质粒载体pIRESgpt为模板,扩增获得LoxPCMVgptIRESLoxP基因表达盒(约2.9kb),将其克隆入质粒pBUS10(含有MDVUS10区)的BalI位点,获得重组质粒pUSgptIRES(L);对重组质粒pUSgptIRES(L)进行测序分析,发现两同向的loxP位点正确插入到pUSgptIRES(L)中;将含有完整的GFP基因以及polyA尾的基因片段,连入pUSgptIRES(L)中,把gpt基因替换掉,从而获得重组质粒pUSGFPIRES(L)。将转移载体pUSGFPIRES(L)瞬时转染CHO细胞,可以观察到绿色荧光,说明GFP基因获得有效表达;将pUSGFPIRES(L)转染已感染MDVCVI988株的CEF细胞,可以筛选到表达绿色荧光蛋白的重组病毒;通过测定重组病毒在细胞上的生长曲线,发现重组病毒与亲本毒生长曲线相吻合。为进一步探讨MDV在体内的特性奠定基础,同时,为Cre/LoxP重组酶系统在MDV中的应用奠定基础。The expressing cassette, LoxP-CMV-gpt-IRES-LoxP( about 2.9kb), was amplified by PCR from a plasmid, pIRES-gpt, by use of the primers , which contained the loxP sites in 5' terminals, respectively. The loxP sites were designed into primers by the software of Primer primer 5.0. Then the cassette was cloned into the site of BalⅠ in pBUS10 to obtain pUS-gptIRES(L). The sequencing analysis for pUS-gptIRES(L) indicated that two loxP sites with the same direction were correctly inserted into pUS-gptIRES (L). The gpt gene in pUS- gptIRES(L) was replaced by a fragment including the full length GFP gene as well as SV40 poly A sequence to get pUS-GFPIRES(L), pUS-GFPIRES(L) was transiently transfected into CHO cell lines, and then the green fluorescence could be seen, the results showed that GFP gene could be expressed correctly. Moreover, pUS- GFPIRES(L) was transfected into the CEF infected MDV CVI988 strain and recombinant virus was selected by the green fluorescence. The growth curve of virus showed the characteristic of recombinant virus was the same as that of CVI988 in vitro. These results give the basis for further studying the characteristic of MDV in vivo and the application of the Cre/LoxP system to MDV genome.
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