LEDGFp52-siRNA真核表达载体的构建和鉴定(英文)  

Construction and identification of the eukaryotic expression vector carrying specific siRNA of LEDGF p52 gene

作　　者：赵海生[1] 王一[1] 

机构地区：[1]第三军医大学西南医院眼科,中国重庆市400038

出　　处：《国际眼科杂志》2006年第5期975-978,共4页International Eye Science

摘　　要：目的: 构建 LEDGFp52 基因 RNA 干扰(RNAi)的真核细胞表达载体。方法: 以 LEDGFp52 为靶基因, 以 pGenSil-l 质粒为载体, 设计构建重组体, 根据 GenBank 数据库提供的LEDGFp52 基因核苷酸序列, 按照 Tuschl 设计原则, 选择设计两条带发夹结构的核苷酸序列, 克隆到空载体pGenSil-l 中, 转化 DH5α菌株, 提取质粒, 进行限制性内切酶酶切鉴定和测序分析。结果: 经酶切鉴定筛选出的重组体测序结果与目的序列完全一致, 重组载体构建成功,重组质粒转染 HeLa 细胞48h, Western blotting 检测到 LEDGFp52 蛋白表达的改变。结论: 利用 RNAi 技术可成功构建抑制 LEDGFp52 表达的小干扰 RNA 重组体。AIM： To construct and identify LEDGFp52 eukaryotic ex- pression vector for RNA interference. METHODS： Recombinants were designed and established by targeting gene LEDGFp52 and plasmid pGensil-1 based on LEDGFp52 cDNA sequences of Genomes. Two pairs of oligonucleotides were synthesized according to the Tuschl principle and inserted into plasmid pGenSil-I to generate siRNA eukaryotic expression vector. DHSa strains were transformed, plasmids were extracted, and recombinant vectors were identified by the restriction map and the sequence anal- ysis. The cultured cells were transfected by the recombinant plasmid （pGensiI-1-RNA.LEDGFp52-1）. At 48 hours after trans- fection, the whole cell protein was extracted, and the protein level was detected using Western blotting with mouse anti-hu- man LEDGFp52 monoclonal antibody. RESULTS： Recombinant plasmids completely concord with the designs by the restriction map and the sequence analysis, the protein level of LEDGFp52 was down regulated at 48 hours after transfecting pGensil-1- LEDGFp52-1 expression vector into HeLa cells, the recombinant eukaryotic expression vectors were successfully constructed. CONCLUSION： siRNA recombinant can be successfully constructed by RNAJ technique to inhibit the expression of LEDGFp52.

关 键 词：LEDGFp52 RNA干扰 真核表达载体 构建 鉴定 

分 类 号：R346[医药卫生—基础医学]