猪白细胞介素-2基因的克隆及其重组禽痘病毒载体的构建  

Cloning of Porcine IL-2 Gene and Its Construction of Recombinant Fowlpox Viruses Vector

作　　者：王淑娟[1] 陈红英[1] 魏战勇[1] 刘金朋[1] 耿静微[1] 崔保安[1] 

机构地区：[1]河南农业大学牧医工程学院,河南郑州450002

出　　处：《华北农学报》2011年第5期71-75,共5页Acta Agriculturae Boreali-Sinica

基　　金：国家"十一五"科技支撑计划专项(2006BAD06A08)

摘　　要：采用RT-PCR技术自豫南黑猪脾淋巴细胞中扩增猪IL-2基因(pIL-2),RT-PCR产物进行T-A克隆并测序,获得了猪IL-2基因序列。将BamHⅠ酶切的猪IL-2基因非定向克隆到BamHⅠ酶切并去磷酸化的pSY538载体上,通过PCR、酶切和测序鉴定,筛选正向插入的重组质粒pSY538/pIL-2。NotⅠ酶切pSY538/pIL-2后,得到含有双启动子LP2和EP2的猪IL-2基因片段,将其亚克隆到含有LacZ基因的pSY681载体上,筛选正向插入的重组禽痘病毒转移质粒pSY681/pIL-2。测序结果表明,克隆的豫南黑猪IL-2基因长482 bp,包含1个完整读码框(465 bp),与GenBank中其他5条猪IL-2基因核苷酸同源性为99.9%。重组质粒pSY681/pIL-2经酶切、测序鉴定,证实含有目的片段,且连接、构建正确。成功构建了重组禽痘病毒转移质粒pSY681/pIL-2,为猪IL-2生物学功能的进一步研究和开发奠定基础。Porcine IL-2 gene was amplified by RT-PCR from the total RNA extracted from the splenocyte of Yu＇ nan pig. The PCR product was cloned and sequenced. The porcine IL-2 （plL-2）gene was digested by BamH I and cloned into pSY538 vector which was digested by BamH I and dephosphorized by calf alkaline phosphatase. By means of the PCR,restriction enzyme digestion and sequencing,the recombinant plasmid pSY538/pIL-2 was selected. After pSY538/pIL-2 was digested by Not I ,the pIL-2 fragment containing LP2 and EP2 was achieved and subcloned into pSY681 vecter containing LacZ gene,then the recombinant plasmid pSY681/pIL-2 was developed. The results indicated that the cloned plL-2 gene had 482 bp,including one ORF（465 bp）. The IL-2 gene sequence of Yu＇nan pig had 99.9% nucleotide homology with the 5 pig IL-2 genes published in GenBank. Enzyme digestion and DNA sequencing results confirmed that the sequence of the recombinant plasmid pSY681/pIL-2 contained the target fragment,and the ligation part was correct. The results showed that the recombinant plasmid pSY681/plL-2 was constructed correctly, paving the way for further study of biological function and further application of porcine IL-2.

关 键 词：猪白细胞介素-2 克隆 重组禽痘病毒 载体 构建 

分 类 号：S828.2[农业科学—畜牧学] Q782[农业科学—畜牧兽医]