畜牧兽医学报 ›› 2006, Vol. 37 ›› Issue (4): 352-355.doi:

• 预防兽医 • 上一篇    下一篇

猪细胞因子cDNA表达文库的构建及其基因的克隆鉴定

夏小慧; 景志忠; 王 勤; 窦永喜   

  1. 1. 中国农业科学院兰州兽医研究所家畜疫病病原生物学国家重点实验室/甘肃省动物寄生虫病重点实验室,兰州 730046; 2. 兰州大学生命科学学院,兰州 730000
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2006-04-25 发布日期:2006-04-25

Construction of cDNA Expression Library of Porcine Cytokine and Cloning of Related Genes

XIA Xiao-hui; JING Zhi-zhong;WANG Qin; DOU Yong-xi
  

  1. 1.Key Laboratory of Veterinary Parasitology of Gansu Province,State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences,Lanzhou 730046, China; 2. School of Life Science,Lanzhou University, Lanzhou 730000, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2006-04-25 Published:2006-04-25

摘要: 为克隆和研究猪细胞因子及相关基因,应用建库试剂盒成功构建了猪细胞因子cDNA表达文库。采取健康猪外周血及淋巴结,分离单个核细胞,经LPS+PHA联合刺激不同时间后,提取总RNA。将各组样品混合,分离纯化mRNA。反转录合成cDNA第一链和第二链,与EcoRI和HindⅢ接头连接。酶切和过柱分级分离后,与λScreen载体连接,经体外包装转染E.coli ER1647宿主菌,进行文库容量测定和扩增。以扩增文库的DNA为模板,利用已知基因引物克隆猪IL-2和IL-4的cDNA并进行测序。结果表明,成功构建了猪细胞因子cDNA文库,文库原始库容量为8×105,插入片段在300~2 000 bp,扩增得到特定的IL-2和IL-4基因,说明文库质量高、代表性强,为进一步从文库中筛选未知细胞因子及相关基因提供了有效的工具。

Abstract: In order to clone and study the cytokine and related genes of porcine, a cDNA library of porcine cytokine was constructed. The mononuclear cells were isolated from the peripheral blood and lymph nodes of healthy porcine and were stimulated by PHA+LPS at different time. The total RNA were extracted and the mRNA were isolated. Single-strand cDNA and double-strand cDNA were synthesized from mRNA, then ligated to directional EcoRI and HindⅢ linkers. cDNA were ligated into λScreen vector after size fractionating by gel filtration and packaged in vitro. The cloning efficiency was evaluated and the length of the cDNA fragment was assayed by PCR. Using the amplified library as template DNA, 2 pair primers were designed according to the sequence of the porcine IL2 and IL4, then the gene were amplified by PCR.The results demonstrated that a cDNA library of porcine cytokine has been constructed and the IL2 and IL4 gene were amplified successfully. The tilter of the cDNA library was 8×105 pfu/mL and the length of inserts was about 300~2 000 bp. It is helpful in the further study on screening novel cytokine and related genes.