| 陈芳芳1 李俐2 陈慧珍1 肖成华3 高殿帅1△.神经粘附分子NCAM140 基因RNA干扰质粒的构建与鉴定[J].现代生物医学进展英文版,2014,14(2):251-255. |
| 神经粘附分子NCAM140 基因RNA干扰质粒的构建与鉴定 |
| Construction and Identification of RNA Interference Vector TargetingNCAM140 Gene |
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| DOI： |
| 中文关键词: NCAM140 RNAi 质粒 |
| 英文关键词: NCAM140 RNA interference Plasmids |
| 基金项目: |
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| 中文摘要: |
| 摘要目的：构建有效的小鼠神经粘附分子（NCAM140）基因的RNA 干扰（RNAi）质粒载体，为研究NCAM140参与的细胞信号通
路转导、其生物学作用以及以NCAM140 为靶点的基因治疗提供稳定转染的RNAi 质粒。方法：使用基因序列软件设计、筛选符
合公开文献筛选参数的4 条靶序列以及1条阴性对照序列，由上海吉玛技术有限公司合成。与载体质粒pGPU6/GFP/Neo 重组后，
分别命名为pSi-nca1、pSi-nca2、pSi-nca3、pSi-nca4和pSi-control。转染大肠杆菌感受态细胞。选择阳性克隆进行DNA 测序鉴定，
Western blot方法进行干扰靶点的筛选。选取干扰效率最高的质粒转染MN9D 细胞，普通光学显微镜分别计数同一视野细胞总数
及GFP阳性细胞数，计算转染效率。结果：酶切和DNA 测序结果证实shRNA正确插入pGPU6/GFP/Neo 质粒；Western blot结果
显示与空质粒对照组比较，pSi-nca4 组细胞NCAM140 表达明显下调，细胞转染效率为62 %。结论：成功构建靶向小鼠
NCAM140 基因的RNAi 质粒，为NCAM140 参与的细胞信号通路的研究以及以NCAM140为靶点的基因治疗提供了稳定转染
细胞的干扰质粒，为研究其生物学作用奠定了分子生物学基础。 |
| 英文摘要: |
| ABSTRACT Objective:To construct RNA interference plasmid targeting NCAM140, it provided stable RNA interference plasmid
for NCAM140 study involved in cell signaling pathway, function of molecular biology and NCAM140-targeting gene therapy.Methods:
4 gene sequences and 1 non-sence control gene sequence consistent with the screening features described in previous articles using open
websites were designed, and the sequences were synthesized with the GenePharma Company. The sequences were amplified in Bacterium
coli after gene recombination with pGPU6/GFP/Neo plasmid, and were named as pSi-nca1, pSi-nca2, pSi-nca3, pSi-nca4 and
pSi-control respectively. Those plasmids were transfected into E. coli competent cells and positive clones were selected for DNA sequencing.
After sequencing identification, the positive clones were transfected into MN9D cells. The GFP positive percentages (GFP positive
cells versus total number of MN9D cells) were used to determine the transfer efficiency of these plasmids, and the inhibitory efficiency
of these plasmids were confirmed by western blot. Results:shRNA was inserted into plasmid pGPU6/GFP/Neo correctly confirmed
by digestion and DNA sequencing. The protein level of NCAM140 in MN9D cells at 24 hr after transfected into pSi-nca4 Plasmid
is depressed (P <0.001). The most efficient plasmid was pSi-nca4. The pSi-nca4 transfection efficiency was 62 %.Conclusion: RNA interference
plasmid targeting NCAM140 is successfully constructed, it provides stable RNA interference plasmid for the research of
NCAM140 participating in cell signaling pathway, and offers favorable tool for the research of NCAM 140 biological effects and
NCAM140-targeting gene therapy. |
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