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当前位置: 首页 > 文章 > 奶牛溶菌酶基因(Lyz)乳腺特异性表达质粒构建与鉴定 家畜生态学报 2019 (5) 24-28
Position: Home > Articles > 奶牛溶菌酶基因(Lyz)乳腺特异性表达质粒构建与鉴定 Journal of Domestic Animal Ecology 2019 (5) 24-28

奶牛溶菌酶基因(Lyz)乳腺特异性表达质粒构建与鉴定

作  者：
张志鹏;江静宜;夏海磊;冀德君;李明勋;杨章平
关键词：
奶牛乳房炎;溶菌酶;乳腺特异性表达载体;基因治疗
摘  要：
研究旨在构建具有高效抗菌、活性持久的奶牛乳腺特异性表达质粒,探索研制新型抗菌制剂,为利用基因工程技术防治奶牛乳房炎提供重要材料.根据GenBank中奶牛溶菌酶基因(lysozyme,Lyz)mRNA序列(GenBank号:NM180999.1)设计引物,从奶牛乳腺上皮细胞中RT-PCR扩增Lyz基因编码序列,将其克隆到携带增强型绿色荧光蛋白通用型表达载体pEGFP-N1中测序.重组质粒pEGFP-N1-Lyz经Ase I+Hind III双酶切除CMV启动子,将奶牛乳腺特异性表达β-乳球蛋白基因(BLG)启动子同源重组替换到Ase I和Hind III酶切位点,构建奶牛溶菌酶基因(Lyz)乳腺特异性表达质粒pBLG-EGFP-N1-Lyz,采用脂质体法转染奶牛乳腺上皮细胞(BMEC)、人肾脏上皮细胞(HEK293T),荧光显微镜检测转染细胞中绿色荧光蛋白的表达情况.结果表明,重组表达质粒pBLG-EGFP-N1-Lyz测序结果与目的片段长度相符,转染至BMEC细胞和HEK293T细胞,在奶牛乳腺上皮细胞观察到绿色荧光, HEK293T细胞未观察到绿色荧光,奶牛Lyz基因乳腺特异性表达质粒构建成功.
作  者：
ZHANG Zhipeng;JIANG Jingyi;XIA Hailei;JI Dejun;LI Mingxun;YANG Zhangping;College of Animal Science and Technology,Yangzhou University;
关键词：
cow mastitis;;lysozyme;;mammary gland specific expression vector;;gene therapy
摘  要：
The purpose of this study was to construct the specific expression plasmid of dairy cow mammary gland with high efficiency and lasting activity, to explore the development of novel antibacterial agent, and to provide important materials for the prevention and treatment of dairy cow mastitis by genetic engineering technology. According to the mRNA sequence of cow Lyz gene in GenBank(NM_180999.1), a primer was designed, and the coding sequence of Lyz gene was amplified from bovine mammary epithelial cells by RT-PCR. The Lyz gene was cloned and sequenced into pEGFP-N1, a universal expression vector carrying enhanced green fluorescent protein. The recombinant plasmid pEGFP-N1-Lyz was removed from the CMV promoter by Ase I and Hind III double enzyme, and the homologous recombination of the(BLG) promoter expressing β-lactoglobulin gene was replaced by AseI and Hind III restriction sites. The(Lyz) mammary specific expression plasmid pBLG-EGFP-N1-Lyz of bovine lysozyme gene was constructed and transfected into dairy mammary epithelial cells(bMEC)and HEK293 T cells by liposome method. The expression of green fluorescent protein in transfected cells was detected by fluorescence microscope. The results showed that the pBLG-EGFP-N1-Lyz sequence of the recombinant expression plasmid was consistent with the length of the target fragment. The recombinant plasmid was transfected into bovine mammary epithelial cells and HEK293 T cells. Green fluorescence was observed in bovine mammary epithelial cells,but no green fluorescence was observed in HEK293 T cells. The mammary gland specific expression plasmid of dairy cow Lyz gene was successfully constructed.

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