贵州医科大学学报

2012, v.37;No.159(06) 587-592

[打印本页] [关闭]
本期目录(Current Issue) | 过刊浏览(Past Issue) | 高级检索(Advanced Search)

Mpl基因RNA干扰载体的构建及荧光显微镜筛选
Construction of Mpl Gene RNA Interference Vector and Selecting Effective Mpl-specific shRNA with Fluorescence Microscopy

邹宇光;莫玉叶;庞实锋;张强;杨芳;易文君;何国锋;喻巍巍;郑克勤;
ZOU Yuguang1,MO Yuye1,PANG Shifeng1,ZHANG Qiang2,YANG Fang3, YI Wenjun1,HE Guofeng1,YU Weiwei1,ZHENG Keqin1(1.Department of Biology,Guangdong Medical College,Zhanjiang 524023,Guangdong,China;2.Mai Rui Biology Medical Treatment Electron Limited Company of Shenzhen,Shenzhen 518057,Guangdong,China; 3.Yushan Middle School of Guangzhou City,Guangzhou 511400,Guangdong,China)

摘要(Abstract):

目的:建立荧光显微镜快速筛选对血小板生成素受体(Mpl)基因RNA干扰片段的方法。方法:通过体外重组技术将Mpl与绿色荧光蛋白(GFP)构建成融合基因,克隆进pDs载体中产生pDs-Mpl-GFP载体,将人U6启动子及5个Mpl shRNA发夹结构(shMpl-A,shMpl-B,shMpl-C,shMpl-D,shMpl-E)分别克隆至pDs-Mpl-GFP真核载体中,构建出针对Mpl 5个不同位点的RNA干扰载体,然后将获得的上述干扰载体通过脂质体方法转染至293T细胞中,用荧光显微镜观察293T细胞的荧光发光强度及荧光细胞数,判定构建的RNA干扰载体对靶基因RNA的干扰效果。结果:构建的5个干扰载体都能对转染的293T细胞中的Mpl-GFP融合基因进行有效的基因敲减作用,在pDs-Mpl-GFP-TK-U6-shMpl-A、pDs-Mpl-GFP-TK-U6-shMpl-B与pDs-Mpl-GFP-TK-U6-shMpl-E的干扰作用下,293T细胞中的荧光强度及发荧光细胞数目变得更少和更弱,干扰效果较好,而其它两个效果较差;在这三个较好的干扰载体中,pDs-Mpl-GFP-TK-U6-shMpl-A的干扰效果最好。结论:成功构建Mpl基因的真核RNA干扰载体,并筛选出有效的RNA干扰片段。
Objective: To establish a method for selecting effective Mpl-specific shRNA with fluorescence microscopy quickly.Methods: Mpl and green fluorescent protein(GFP) fused genes were constructed with recombination technique in vitro.Mpl-GFP fused genes was cloned into pDs vector resulting in pDs-Mpl-GFP.Human U6 promoter and five Mpl-specific shRNA(shMpl-A,B,C,D,E) were cloned into pDs-Mpl-GFP vector separately to obtain five RNA interference vectors aiming at different sites of Mpl gene.Then,vectors were transfected into 293T cells with liposome method.Take advantage of luminescence characteristic of GFP in these vectors,fluorescence intensity and the amount of fluorescent cells were detected under fluorescence microscopy to judge the effects of the shRNA.Results: The results showed that all the five vectors had knocking down effects on Mpl-GFP fusion protein in 293T cells,and fluorescence intensity and amount of fluorescent cells interfered by shMpl-A,B,E were less and weaker than those interfered by others.The effects of others were poor.The effect of shMpl-A was the best in them.Conclusions: The Mpl-specific shRNA interference vectors are successfully constructed and effective interference fragment is screened under fluorescence microscopy.

关键词(KeyWords): 绿色荧光蛋白;RNA干扰;基因融合
green fluorescent protein;RNA interference;gene fusion

Abstract:

Keywords:

基金项目(Foundation): 教育部科学技术研究重点项目(210156);; 广东省大学生创新实验项目(KY1003);; 广东省卫生厅青年基金(B2010235);; 湛江市科技攻关项目(2010C3111005)

作者(Author): 邹宇光;莫玉叶;庞实锋;张强;杨芳;易文君;何国锋;喻巍巍;郑克勤;
ZOU Yuguang1,MO Yuye1,PANG Shifeng1,ZHANG Qiang2,YANG Fang3, YI Wenjun1,HE Guofeng1,YU Weiwei1,ZHENG Keqin1(1.Department of Biology,Guangdong Medical College,Zhanjiang 524023,Guangdong,China;2.Mai Rui Biology Medical Treatment Electron Limited Company of Shenzhen,Shenzhen 518057,Guangdong,China; 3.Yushan Middle School of Guangzhou City,Guangzhou 511400,Guangdong,China)

Email:

DOI: 10.19367/j.cnki.1000-2707.2012.06.003

文章评论(Comment):

序号(No.) 时间(Time) 反馈人(User) 邮箱(Email) 标题(Title) 内容(Content)
反馈人(User) 邮箱地址(Email)
反馈标题(Title)
反馈内容(Content)
扩展功能
本文信息
服务与反馈
本文关键词相关文章
本文作者相关文章
中国知网
分享