基础医学与临床 ›› 2013, Vol. 33 ›› Issue (11): 1440-1445.

• 研究论文 • 上一篇    下一篇

hTERT和Survivin双靶点RNAi表达载体的构建及对人结肠癌SW480细胞的抑制作用

王平,肖琳,董俊红,孙凤祥,蒋吉英,王守训   

  1. 潍坊医学院
  • 收稿日期:2013-01-31 修回日期:2013-09-17 出版日期:2013-11-05 发布日期:2013-10-28
  • 通讯作者: 王守训 E-mail:wangping197820022002@yahoo.com.cn
  • 基金资助:
    Survivin与hTERT双靶点RNAi在SW480细胞凋亡及增殖中的作用研究

Construction of double interference vector targeting both Surviving and hTERT gene and its inhibitory effect on human colon cancer cell line SW480

  • Received:2013-01-31 Revised:2013-09-17 Online:2013-11-05 Published:2013-10-28

摘要: 目的 构建人端粒酶反转录酶(hTERT)和生存素(Survivin)基因表达的RNA共干扰载体,并检测其对人结肠癌SW480细胞中hTERT基因和Survivin基因的干扰作用。 方法 根据Genbank提供的hTERT和 Survivin cDNA序列,设计、筛选出高效、特异性强的干扰序列,构建特异性干扰hTERT基因和Survivin基因的重组体pGenesil-1.1-Survivin、pGenesil-1.2-hTERT,酶切、测序鉴定正确后,两个重组体均用HindIII和BamHI双酶切,将pGenesil-1.1-Survivin回收大片段,pGenesil-1.2-hTERT回收小片段,将回收大、小片段用T4 DNA连接酶定向连接,即构建成重组体pGenesil1.1-Survivin-hTERT。将3个重组体分别转染SW480细胞,RT-PCR检测细胞中hTERT和Survivin基因表达水平,MTT检测对SW480细胞增殖的影响。 结果 构建的各质粒经限制性酶切及DNA 测序均证明其质粒构建正确,RT-PCR检测hTERT和Survivin基因表达水平明显降低(P<0.05),各干扰质粒重组体对细胞增殖有明显的抑制作用(P<0.05)。 结论 靶向Survivin和hTERT基因的双干扰载体构建成功,为后续的结肠癌基因治疗研究奠定理论基础。

关键词: 双靶点RNA干扰, survivin, hTERT

Abstract: Objective To construct the double interference vector targeting both survivin and hTERT gene and detect its silencing effects on surviving and hTERT gene in human colon carcinoma SW480 cell line. Methods Two effective targeting sequences were chosen according to hTERT and surviving cDNA sequences in Gen Bank, Then they were inserted into pGenesil-1.1 and pGenesil-1.2, pGenesil-1.1-survivin and pGenesil-1.2-hTERT were constructed. The recombinant plasmids were identified by restriction endonuclease and DNA sequencing. pGenesil-1.1-survivin and pGenesil-1.2-hTERT were digested by HindIII and BamHI separately, long fragment of pGenesil-1.1-survivin and small fragment of pGenesil-1.2-hTERT were collected. Then long fragment and small fragment were connected with T4 DNA ligase orientation, the double interference vector pGenesil1.1-survivin-hTERT was constructed. These siRNA recombinant expression vector separately were transfected into SW480 cell line, The effect of siRNA recombinant expression vector was detected by RT-PCR and MTT. Results By restriction endonuclease and DNA sequencing, specific RNAi expression vector targeting survivin and hTERT gene was constructed correctly. The growth rate of SW480 cells transfected with siRNA recombinant expression vector was significantly decreased. Conclusion The multiple siRNA recombinant expression vector targeting hTERT and Survivin gene simultaneously has been constructed successfully.This result could provide theoretical information for the further research.

Key words: double inierferenee siRNA, survivin, hTERT

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