Article Summary
张 熠 杨 靖 吕运成 钟 警 文格波.hsa-miR-20a 低表达慢病毒载体的构建及其表达鉴定[J].现代生物医学进展英文版,2015,15(5):804-807.
hsa-miR-20a 低表达慢病毒载体的构建及其表达鉴定
Construction of a Recombinant Lentiviral Vector to Inhibit hsa-miR-20aExpression and Validation of its Transduction Efficiency
  
DOI:
中文关键词: Hsa-miR-20a  慢病毒载体  HL-60
英文关键词: Hsa-miR-20a  Lentivirus  HL-60
基金项目:国家自然科学基金项目( 81 100560)
Author NameAffiliation
张 熠 杨 靖 吕运成 钟 警 文格波 南华大学附属第一医院内分泌科南华大学人体解剖学教研室南华大学附属第一医院临床医学研究所 
Hits: 1045
Download times: 1097
中文摘要:
      目的: 构建 hsa-miR-20a 低表达慢病毒载体, 检测其在 HL-60 中表达。 方法: 采用 In-fusion 重组交换克隆法设计并合成 hsa-miR-20a 前体序列 的扩增引物, 扩增获得目 的片 段插入慢病毒 GV159 中, 得到 重组的 LV-hsa-miR-20a 表达载体, 通过与包装 质粒共转染 293T 细胞, 获得携带 hsa-miR-20a 的重组慢病毒并测定病毒滴度。 取对数生长期 HL-60 细胞根据病毒滴度及细胞 MOI 值感染慢病毒, 感染后 24 h、48 h、72 h、96 h 镜下观察荧光表达情况, 判断感染效率, qRT-PCR 检测 HL-60 细胞 hsa-miR-20a 的表达变化。 结果: 成功构建 LV-hsa-miR-20a 低表达慢病毒载体,其病毒滴度为 (8E+8)TU/mL。 该病毒感染 HL-60 细胞的效率可 高达到 80%, 并可有效降低 HL-60 细胞 hsa-miR-20a 表达水平。 结论: 成功构建了 hsa-miR-20a 低表达慢病毒载体,包被的慢病毒 可以在 HL-60 细胞中实现低表达效果, 为后续功能研究奠定了 基础。
英文摘要:
      Objective:To construct a recombinant lentiviral vector to inhibit hsa-miR-20a expression and validation of its transduction efficiency in HL-60.Methods:Based on BD In-FusionTM PCR cloning method, we designed and synthesized hsa-miR-20a gene with its promoter, then cloned it into a lentivirus vector GV1 59. After being conformed, the LV-hsa-miR-20a plasmid was co-transfected with packaging plasmid into 293T cells to obtain hsa-miR-20a lentivirus vector. Recombinant lentivirus was added to logarithmic growth phase HL-60 cells according to virus titer and MOI (multiplicity of infection) value, and its infection efficiency and hsa-miR-20a level were tested by fluorescent observation and real-time quantitative PCR respectively.Results:Hsa-miR-20a lower expressive lentiviral vector was constructed successfully, and virus titer was (8E+8)TU/mL. The infection efficiency of Recombinant lentiviruse in HL-60 cells reached 80%, and the expression level of hsa-miR-20a reduced effectively.Conclusion:The letiviral vector containing hsa-miR-20a with low expression was successfully constructed, which will be useful for researching the function of hsa-miR-20a in the future.
View Full Text   View/Add Comment  Download reader
Close