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中国临床药理学与治疗学 ›› 2006, Vol. 11 ›› Issue (6): 655-658.

• 研究原著 • 上一篇    下一篇

胰腺癌Bx-PC3细胞Survivin基因ShRNA质粒表达载体的构建

黄鹤, 吴佩, 洪书剑, 茆家定, 芮景   

  1. 皖南医学院附属弋矶山医院普外科, 芜湖 241000, 安徽
  • 收稿日期:2006-04-13 修回日期:2006-06-05 出版日期:2006-06-26 发布日期:2020-12-04
  • 通讯作者: 吴佩,主任医师,硕士生导师,研究方向:肝胆胰外科。Tel:0553-5738343 E-mail:wp708@sina.com
  • 作者简介:黄鹤,硕士,主治医师,研究方向:肝胆胰外科。Tel:0553-5738343 E-mail:huanghe1971@126.com

Construction of eukaryotic expression vector expressing double shRNA sections targeting Survivin gene in Bx-PC3 cells

HUANG He, WU Pei, HONG Shu-jian, MAO Jia-ding, RUI Jing   

  1. Department of General Surgery, Yijishan Hospital, Wannan Medicl College, Wuhu 241000, Anhui, China
  • Received:2006-04-13 Revised:2006-06-05 Online:2006-06-26 Published:2020-12-04

摘要: 目的: 构建针对胰腺癌Bx-PC3 细胞Survivin基因2 条shRNA 的质粒表达载体。方法: 以Survivin基因为靶点, 通过自行设计并构建包含两段短发夹状RNA (small hairpin RNA, shRNA), 携带有各自的U6 启动子和终止码、共同的绿色荧光蛋白(green fluorescent protein, EGFP) 基因和Neo 基因的pGenesil-1 Survivin shRNA 载体, 利用脂质体介导的方法转染人胰腺癌Bx-PC3 细胞, RT-PCR 观察其对Bx-PC3细胞Survivin 基因表达的影响。结果: HE1 质粒和HE2 质粒的酶切鉴定正确, 质粒转化菌液HE1、HE2进行测序分析均为插入正确的克隆质粒。胰腺癌Bx-PC3 细胞转染成功, 转染细胞后Survivin mRNA的表达有明显抑制。结论: 实验构建针对胰腺癌细胞Survivin 基因2 条shRNA 的质粒表达载体成功。

关键词: Survivin 基因, RNA 干扰, 短发夹RNA, 胰腺癌细胞

Abstract: AIM: To construct eukaryotic expression vector expressing double shRNA sections targeting Survivin gene.Methods: Eukaryotic expression vector expressing double shRNA sections targeting Survivin gene were designed and chemically synthesized.They were directionally inserted into plasmid pGenesil-1 with respectively U6 promoter and termination code, the common green fluorescence protein (EGFP) gene and Neo gene. In this way, the vector of pGenesil-1 shRNA containing 2 sections of Survivin shRNA were constructed and they were transfected into the pancreatic cancer cell Bx-PC3. Transfection was detected by fluorescence microscope. The inhibition expression of Survivin mRNA was measured by RT-PCR.Results: HE1 and HE2 plasmids were identified by the biocatalyst cut which confirmed the exactitude and were analyzed by the sequence analysis which verified the perfect clone plasmid inserted by them.Conclusion: A eukaryotic expression vector of double short hairpin RNA for Survivin gene is successfully constructed.The pancreatic cancer cells Bx-PC3 succeed to be transfected and expression of Survivin mRNA is inhibited obviously.

Key words: Survivin gene, RNA interference, small hairpin RNA, pancreatic cancer cell

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