You Position: Home > Paper

Construction of the alpha-fetoprotein enhancer controlled gene therapy vector specific for hepatocellular carcinoma and identification of its activity

( views:264, downloads:4 )
Author:
No author available
Journal Title:
WORLD CHINESE JOURNAL OF DIGESTOLOGY
Issue:
33
DOI:
10.3969/j.issn.1009-3079.2007.33.004
Key Word:
甲胎蛋白;启动子;增强子;克隆;聚合酶链式反应;载体;肝癌

Abstract: 目的:构建新型AFP顺式作用元件调控的基因表达载体,检测该调控元件的特异性和活性表达.方法:设计含有特定酶切位点的引物,采用PCR法从HepG2细胞中克隆AFP启动子及增强子基因亚区片段.启动子与增强子长、短片段分别与含有报告基因荧光素酶基因的载体pGL-3的多克隆位点连接,构建不同长度hAFP增强子调控的肝癌特异性Luciferase表达载体APSE-Luc/APLE-Luc.经测序,PCR及酶切鉴定各重组体.用脂质体法将表达载体转染表达或不表达AFP的肿瘤细胞系进行荧光强度及特异性表达测定.结果:成功地将AFP基因启动子、增强子克隆到报告基因载体pGL-3的多克隆位点,构建成为不同长度hAFP增强子调控的肝癌特异性Luciferase表达载体APSE-Luc/APLE-Luc,酶切鉴定和DNA序列分析无误.转染APLE-Luc质粒的细胞中Luciferase表达量明显高于转染APSE-Luc质粒的细胞,其在HepG2细胞中的表达明显高于SMMC7721细胞及Hela细胞.结论:成功构建AFP启动子与增强子联合调控载体APSE-Luc/APLE-Luc.AFP增强子能够特异性地增强目的基因在AFP阳性细胞中表达,并且不同的亚区活性不同,长片段的活性明显高于短片段.

WanfangData CO.,Ltd All Rights Reserved
About WanfangData | Contact US
Healthcare Department, Fuxing Road NO.15, Haidian District Beijing, 100038 P.R.China
Tel:+86-010-58882616 Fax:+86-010-58882615 Email:yiyao@wanfangdata.com.cn