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Survivin反义RNA真核表达载体的构建及鉴定
引用本文:王晓娟,戴国仪,赵晓平,于慧玲,王国华,朱慧芬,张悦,沈关心.Survivin反义RNA真核表达载体的构建及鉴定[J].中德临床肿瘤学杂志,2003,2(4):246-249,254.
作者姓名:王晓娟  戴国仪  赵晓平  于慧玲  王国华  朱慧芬  张悦  沈关心
作者单位:武汉华中科技大学同济医学院免疫学系 430030 (王晓娟,戴国仪,赵晓平,于慧玲,王国华,朱慧芬,张悦),武汉华中科技大学同济医学院免疫学系 430030(沈关心)
基金项目:This project was supported by a grant from National Key Basis Research Program of China(No.CB 513109)and the National Natural Sciences Foundation of China(No.39970693).
摘    要:目的 为了特异封闭白血病细胞survivin的表达,抑制其功能,本实验构建了survivin反义核酸载体并导入白血病细胞系中。方法 应用RT—PCR获得survivin的cDNA片段,反向插入pcDNA3质粒载体中;经限制性酶切和测序鉴定所构建的反义核酸是否正确;采用电转染方法将重组体导入HL—60细胞中;RT—PCR技术检测转染细胞survivin表达的变化。结果 经限制性酶切和测序鉴定证明survivin反义核酸已成功构建;RT—PCR产物电泳结果显示,与转染前细胞、空质粒转染细胞相比,转染survivin反义核酸的细胞survivin mRNA水平明显降低。结论 本实验已成功建立了survivin反义核酸真核表达载体,而且在白血病细胞系中发挥了特异封闭作用,为进一步研究survivin反义核酸在白血病治疗中的作用提供了实验基础。

关 键 词:Survivin  反义RNA  真核表达载体  鉴定  白血病  RT-PCR
收稿时间:12 September 2002

Construction and characterization of an antisense RNA eukaryotic expression vector for survivin
Wang?Xiaojuan,Dai?Guoyi,Zhao?Xiaoping,Yu?Huiling,Wang?Guohua,Zhu?Huifen,Zhang?Yue,Shen?Guanxin.Construction and characterization of an antisense RNA eukaryotic expression vector for survivin[J].The Chinese-German Journal of Clinical Oncology,2003,2(4):246-249,254.
Authors:Wang Xiaojuan  Dai Guoyi  Zhao Xiaoping  Yu Huiling  Wang Guohua  Zhu Huifen  Zhang Yue  Shen Guanxin
Institution:(1) Department of Immunology, Tongji Medical College, Huazhong University of Science and Technology, 430030 Wuhan, China;(2) Hospital of Inner Mongolia Agricultural University, 010040 Hohhot, China;(3) Department of Immunology, Inner Mongolia Medical College, 010059 Hohhot, China
Abstract:Objective: To inhibit specifically survivin expression and block its function in leukemia cells, an antisense RNA expression plasmid for survivin was constructed and transfected into a leukemia cell line. Methods: A cDNA fragment of survivin obtained by RT-PCR was inserted into a plasmid vector named pcDNA3 in the reverse direction. Antisense RNA of survivin was confirmed by restriction enzyme digestion and DNA sequencing. The recombinant plasmid was transfected into the cell line HL-60 by electroporation. The effect of survivin antisense RNA on survivin mRNA expression in transfected cells was examined by RT-PCR. Results: The correct construction of the recombinant plasmid has been shown by restriction enzyme digestion and DNA sequencing. As compared to controls, the level of survivin mRNA expression in transfected cells decreased significantly. Conclusion: An antisense RNA vector for survivin has been successfully constructed and may be useful as a specific inhibitor in leukemia cells. Thus, antisense therapy on the basis of survivin can be further explored in leukemia.
Keywords:: leukemia  survivin  antisense RNA
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