华北农学报 ›› 2011, Vol. 26 ›› Issue (6): 94-96. doi: 10.7668/hbnxb.2011.06.018

所属专题: 生物技术

• 论文 • 上一篇    下一篇

鸭瘟病毒河南株gG基因的克隆、测序

王岩1,2, 曹素芳2, 崔保安1   

  1. 1. 河南农业大学牧医工程学院, 河南郑州 450002;
    2. 郑州牧业工程高等专科学校医学系, 河南郑州 450011
  • 收稿日期:2011-09-26 出版日期:2011-12-28
  • 通讯作者: 崔保安(1948-),男,河南荥阳人,教授,博士生导师,主要从事动物预防兽医学教学和研究工作。
  • 作者简介:王岩(1970-),男,河南睢县人,讲师,在读博士,主要从事猪禽传染病病原研究。
  • 基金资助:
    2011年度河南省教育厅自然科学研究计划项目(2011B230014)

Cloning and Sequencing of gGGene of Duck Plague Virus HN Strain

WANG Yan1,2, CAO Su-fang2, CUI Bao-an1   

  1. 1. Engineering College of Animal Husbandry and Veterinary Science, Henan Agricultural University, Zhengzhou 450002, China;
    2. Zhengzhou Colloge of Animal Husbandry Engineering, Zhengzhou 450011, China
  • Received:2011-09-26 Published:2011-12-28

摘要: 鸭瘟是鸭的一种急性传染和高致死的病毒性疾病。根据GenBank收录中鸭瘟病毒gG基因序列设计并合成1对引物,以鸭瘟病毒河南分离株DNA为模板,PCR扩增出1条约1 600 bp的含gG基因特异性片段,并将其克隆至PMD19-T载体上。经酶切鉴定,得到含gG基因重组质粒,并对重组阳性质粒进行序列测定。结果表明,gG基因长1 380 bp,该基因编码459个氨基酸,预测分子量为50.5 kDa。gG基因的克隆为进一步研究其生物学功能奠定了基础。

关键词: 鸭瘟病毒, gG基因, 克隆, 测序

Abstract: Duck Plague is an acute contagious and highly lethal virus disease of ducks. According to published Duck Plague Virus gGgene sequences,one pair of specific primers was designed and synthesized. The genomic DNA of DPV Henan strain,which was isolated from Henan,was used as template. Full-length gGgene was amplified by polymerase chain reaction(PCR) and cloned into the PMD19-T vector. The gene was sequenced and the open reading frame of 1 380 bp was determined. it encode 459 amino acids and the predicted protein has an molecular mass of 50. 5 kDa. The clone of gGgene provides foundation for study of its biological function.

Key words: Duck Plague Virus(DPV), gGgene, Cloning, Sequencing

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引用本文

王岩, 曹素芳, 崔保安. 鸭瘟病毒河南株gG基因的克隆、测序[J]. 华北农学报, 2011, 26(6): 94-96. doi: 10.7668/hbnxb.2011.06.018.

WANG Yan, CAO Su-fang, CUI Bao-an. Cloning and Sequencing of gGGene of Duck Plague Virus HN Strain[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2011, 26(6): 94-96. doi: 10.7668/hbnxb.2011.06.018.

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