华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

亚甲基四氢叶酸还原酶基因在小鼠胚胎腭突间充质细胞中沉默效应的研究

肖文林1 石冰2 王?2 郑谦2 黄磊2   

  1. 1.青岛大学医学院附属医院口腔颌面外科, 山东青岛266003;2.四川大学华西口腔医院唇腭裂外科, 四川成都610041
  • 收稿日期:2009-06-25 修回日期:2009-06-25 出版日期:2009-06-20 发布日期:2009-06-20
  • 通讯作者: 石冰,Tel:028-85501462
  • 作者简介: 肖文林(1971-),男,山东人,副主任医师,博士
  • 基金资助:

    国家自然科学基金资助项目(30371552)

Gene expression of methylene tetrahydrofolate reductase and its silencing effect in primary culture mouse embryo palatal mesenchymal cell

XIAO Wen-lin1,SHI Bing2,WANG Yan2, ZHENG Qian2,HUANG Lei2   

  1. 1. Dept. of Oral and Maxillofacial Surgery, The Medical School Hospital of Qingdao University, Qingdao 266003, China; 2. Dept. of Cleft and Palate Surgery, West China College of Stomatology, Sichuan University, Chengdu 610041, China
  • Received:2009-06-25 Revised:2009-06-25 Online:2009-06-20 Published:2009-06-20
  • Contact: SHI Bing,Tel:028-85501462

摘要:

目的构建亚甲基四氢叶酸还原酶(MTHFR)特异性小干扰RNA(siRNA)真核表达载体,体外观察其对MTHFR基因的沉默作用。方法采用基因克隆技术,将合成的特异性MTHFR RNA干扰寡核苷酸序列插入真核表达载体PsiRNA-Hh1neo_G2,构建MTHFR siRNA真核表达载体。应用核转染技术将PsiRNA-MTHFR重组质粒分别导入原代培养的小鼠胚胎腭突间充质(MEPM)细胞。48 h和5 d后用实时定量聚合酶链反应(Real-Time PCR)和Western blot技术检测MEPM细胞内MTHFR mRNA及蛋白水平的表达情况。结果成功构建PsiRNA-MTHFR真核表达载体。经检测48 h和5 d后转染PsiRNA-MTHFR的MEPM细胞MTHFR mRNA及蛋白表达均显著下调。结论构建的RNA干扰真核表达载体能明显干扰MTHFR mRNA及蛋白的表达,为进一步研究MTHFR的功能以及其调控胚胎腭突融合的机制奠定基础。

关键词: 亚甲基四氢叶酸还原酶基因, RNA干扰, 真核表达

Abstract:

Objective To construct a small interfering RNA(siRNA) eukaryotic expression vector specific for methylene tetrahydrofolate reductase(MTHFR) gene and to observe its silencing effect on MTHFR gene. Methods The expression vectors of PsiRNA-MTHFR were constructed by gene recombination and then were nucleofected into the primary cultured MEPM cell. At 48 h and 5 d after nucleofection, the expression of MTHFR in the levels of mRNA and protein was detected by real-time quantitative polymerase chain reaction(Real-Time PCR) and Western blot. Results The eukaryotic expression vector of PsiRNA-MTHFR, which significantly down-regulated mRNA and protein of MTHFR at 48 h and 5 d after nucleofection, were successfully constructed. Conclusion Eukaryotic expression vector of siRNA specific for MTHFR is successfully contructed, which lays the basis for its application in the mechanism research of MTHFR gene regulating embryo palate shelves fusion.

Key words: methylene tetrahydrofolate reducetase gene, RNA interference, eukaryotic expression