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中国农学通报 ›› 2008, Vol. 24 ›› Issue (4): 8-12.

所属专题: 生物技术

• 畜牧 动物医学 蚕 蜂 • 上一篇    下一篇

犬瘟热病毒核衣壳蛋白N基因的真核表达及鉴定

简中友, ,贾 赟,王全凯,徐立秋,吴 斌,肇慧君,李振荣   

  • 收稿日期:2008-03-04 修回日期:2008-03-14 出版日期:2008-04-05 发布日期:2008-04-05

Eukarytic Expression and Identification of Nucleocapsid Protein N Gene of Canine Distemper Virus

Jian Zhongyou, , Jia Yun, Wang Quankai, Xu Liqiu, Wu Bin, Zhao Huijun, Li Zhenrong   

  • Received:2008-03-04 Revised:2008-03-14 Online:2008-04-05 Published:2008-04-05

摘要: 根据GenBank发表的犬瘟热病毒N基因全序列,设计合成了1对特异扩增CDV N基因的引物。以山东泰安分离的CDV-FOX-TA株细胞毒中提取病毒RNA来制模板,利用RT-PCR扩增出了1.6kb的N基因,将其克隆到pIREShyg载体上,构建了pIRES-N真核表达载体。然后通过磷酸钙共沉淀法转染CHO-K1细胞,通过潮霉素筛选得到阳性克隆,间接免疫荧光实验(IFA)鉴定N基因在CHO细胞中的表达,并用RT-PCR方法从转录水平证实N基因在CHO-K1细胞中的表达,最终建立了CHO/ CDV-N细胞株,为犬瘟热病毒的血清学检测和基因疫苗的研制奠定了基础。

关键词: 肉鸡, 肉鸡, 复方杜仲, 免疫器官, ND-HI效价

Abstract: According to the published sequence of N gene of CDV, a pair of primers was designed and synthesized, which can amplify CDV N gene. N gene’s cDNA fragment of about 1.6kb was obtained through RT-PCR from FOX TA strain of CDV, and was cloned into pIREShyg Vector Eukarytic Expression Vector named as pIRES-N was constructed. pIRES-N was transfected into CHO-K1 cells with coprecipitation, and positive cells were screened with hygromycine selection. The N gene protein was expressed in the CHO cells proved by IFA. The N gene was transcripted as proved with RT-PCR. CHO/CDV-N cell strain was constructed, which provided evidence for research of CDV serumal detection and gene vaccine.