| 新城疫病毒HN09-69株P基因的克隆、序列分析及表达 |
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| 引用本文： | 陈礼朋,王忠田,岳旭龙.新城疫病毒HN09-69株P基因的克隆、序列分析及表达[J].西北农林科技大学学报(社会科学版),2012,40(2):20-26. |
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| 作者姓名： | 陈礼朋 王忠田 岳旭龙 |
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| 作者单位： | 河南农业大学 牧医工程学院;中国兽医药品监察所;河南农业大学 牧医工程学院 |
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| 基金项目： | 国家科技支撑计划项目（2006BAD06A08） |
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| 摘 要： | 【目的】对新城疫病毒(NDV)HN09-69株P基因进行克隆、序列分析和表达鉴定，为研究P和V蛋白的功能，及NDV新流行毒株的免疫预防提供理论依据。【方法】以HN09-69株NDV为研究对象，根据GenBank上发布的相关P基因参考序列设计引物，进行RT-PCR扩增、克隆和序列测定分析，将P基因的核苷酸序列与相关参考株的P基因序列进行比对分析并构建进化树。将P基因克隆到原核表达载体PET28a(+)中，得到重组质粒rPET28a(+)-P，将重组表达质粒转化到BL21（DE3）中诱导表达，用SDS-PAGE电泳和Western blotting检测表达情况。【结果】扩增出了HN09-69株P基因的ORF，序列长度为1 188 bp。NDV HN09-69株核苷酸与弱毒株La Sota、clone-30同源性分别为82.5%和82.4%，与强毒株F48E8同源性为84.9%，与鸭源，鹅源NDV核苷酸同源性分别为97.9%～98.4%和96.0%～98.0%。SDS-PAGE电泳和Western blotting检测结果表明，重组P蛋白分子质量约为54 ku,符合预期结果，在大肠杆菌中主要以可溶性的形式表达。【结论】NDV HN09-69株与SDWF-02和SD-09鸭源强毒分离株同源性高，亲缘关系近。重组P蛋白在大肠杆菌中得到了高效表达。
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| 关 键 词： | 新城疫病毒 P基因 原核表达 SDS-PAGE Western blotting |
| 收稿时间： | 2011/8/23 0:00:00 |
Cloning,sequence analysis and expression of Pgene of Newcastle disease virus HN09-69 strain |
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| CHEN Li-peng,WANG Zhong-tian,YUE Xu-long,WANG Ze-ren,GAO Wen-ming,LI Shuang-liang,ZHANG Yu-geng,CUI Bao-an,LI Xin-sheng.Cloning,sequence analysis and expression of Pgene of Newcastle disease virus HN09-69 strain[J].Journal of Northwest Sci-Tech Univ of Agr and,2012,40(2):20-26. |
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| Authors: | CHEN Li-peng WANG Zhong-tian YUE Xu-long WANG Ze-ren GAO Wen-ming LI Shuang-liang ZHANG Yu-geng CUI Bao-an LI Xin-sheng |
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| Institution: | 1(1 College of Husbandry and Veterinary,Henan Agricultural University,Zhengzhou,Henan 450002,China; 2 China Institute of Veterinary Drugs Control,Beijing 100081,China) |
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| Abstract: | 【Objective】 In order to provide support for the prevention new epidemic Newcastle disease virus(NDV) and forming the foundation for study the function of P and V protein,the P gene of NDV HN09-69 was amplified,analyzed and expressed.【Method】 Specific primers were designed according to the reported sequences of NDV in GenBank and the P gene of HN09-69 strain was amplified and sequence was analyzed.Sequence of P gene of HN09-69 strain was compared with relevant reference strains and the phylogenetic tree was constructed.The P gene was cloned into the prokaryotic expression vector PET28a(+).The recombinant plasmids rPET28a(+)-P was constructed,identified and transformed into BL21(DE3)competent cells and induced to expression by IPTG.The expressed protein was detected by SDS-PAGE and Western blotting.【Result】 The complete open read frame(ORF) of P gene was amplified by RT-PCR and contains 1 188 bp in size.The homology of nucleotides was 82.5%,82.4% and 84.9%,respectively.Comparied with duck,goose source NDV,the homology of nucleotides was 97.9%-98.4%,96.0%-98.0%,respectively.The results of SDS-PAGE and Western blotting assay show that the recombinant P protein is about 54 ku in size in accordance with the expected result.【Conclusion】 The NDV HN09-69 strain and Shandong,Heilongjiang virulent strains of source in ducks have high homology and close relationship.The recombinant P protein has high effective expression in E.coli. |
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| Keywords: | NDV P gene procaryotic expression SDS-PAGE Western blotting |
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