【打印本页】 【下载PDF全文】 【HTML】 查看/发表评论下载PDF阅读器关闭

←前一篇|后一篇→

过刊浏览    高级检索

本文已被:浏览 2912次   下载 2125 本文二维码信息
码上扫一扫!
抑癌基因NF2突变子真核表达载体的构建与表达
贺华1,彭彪2,卞留贯1*,孙青芳1,沈建康1,贺子建3,林亦海4
0
(1.上海交通大学医学院附属瑞金医院神经外科,上海 200025;2.广州市第一人民医院神经外科,广州 510180;3.上海瑞金医院集团闵行中心医院神经外科,上海 201100;4.台州市中心医院神经外科,台州 318000)
摘要:
目的:分别构建抑癌基因NF2的42位和47位点突变的2种真核表达载体,并在大鼠神经鞘瘤细胞RT4-D6P2T中诱导表达。方法:用定点突变法分别将pcDNA3.1-NF2第42位赖氨酸(Lys)突变为脯氨酸(Pro),第47位苯丙氨酸(Phe)突变为亮氨酸(Leu)构建2种NF2突变子(pcDNA3.1-NF2ΔLys42Pro和pcDNA3.1-NF2ΔPhe47Leu),将3 种NF2质粒用脂质体法分别转染RT4细胞,RT-PCR和Western印迹法分析NF2基因及蛋白表达,MTT法检测转染后RT4细胞的增殖情况。结果:测序证实定点突变成功,构建的重组真核表达载体pcDNA3.1-NF2ΔLys42Pro和pcDNA3.1-NF2ΔPhe47Leu均能表达相应的蛋白和mRNA,这2种NF2突变体对RT4细胞抑制率明显低于野生型NF2组,差异有统计学意义(P<0.05)。结论:成功构建了2种能够在RT4中表达的单个点突变的NF2基因真核表达载体。
关键词:  NF2  点突变  真核表达载体
DOI:10.3724/SP.J.1008.2008.00546
投稿时间:2008-03-05修订日期:2008-04-11
基金项目:上海市科委启明星跟踪计划(04qmh1414),上海市科委自然科学基金(06ZR14064).
Construction of eukaryotic expression vectors of two NF2 mutants and their expression in rat schwannoma cell line
HE Hua1,PENG Biao2,BIAN Liu-guan1*,SUN Qing-fang1,SHEN Jian-kang1,HE Zi-jian3,LIN Yi-hai4
(1.Department of Neurosurgery,Ruijin Hospital,Shanghai Jiaotong University School of Medicine,Shanghai 200025,China;2.Department of Neurosurgery,The First People’s Hospital of Guangzhou,Guangzhou 510180;3.Department of Neurosurgery,Minhang Central Hospital of Shanghai,Shanghai 201100;4.Department of Neurosurgery,Central Hospital of Taizhou,Taizhou 318000)
Abstract:
Objective:To construct the eukaryotic expression vectors of two NF2 mutants (neurofibromatosisⅡ) and to study their expression in rat schwannoma cell line (RT4).Methods: Site-directed mutagenesis was performed to induce the mutation of the codons for the residue Lys42 in NF2 into Pro in pcDNA3.1-NF2ΔLys42Pro, and convert the codons for Phe 47 into that of Leu.RT4 cells were transiently transfected with the 3 kinds of plasmids containing the mutations and wide-type NF2 via lipofectin separately,then the expression levels of NF2 mRNA and protein were determined by RT-PCR and Western blotting in 3 groups.The cell proliferation was determined by the MTT after transfection.Results: DNA sequence analysis demonstrated the two-step mutagenesis was successful and the two plasmids of pcDNA3.1-NF2ΔLys42Pro and pcDNA3.1-NF2ΔPhe47Leu were obtained,both of the transfectants could produce merlin protein and mRNA.The two mutants had a significantly lower inhibitory rate for RT4 cells compared with wide-type NF2 (P<0.05).Conclusion: The recombinant plasmids pcDNA3.1-NF2ΔLys42Pro and pcDNA3.1-NF2ΔPhe47Leu have been successfully constructed and they can be efficiently expressed in RT4 cells.
Key words:  NF2  point mutation  eukaryotic expression vector