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介导p73去阻抑肽表达的重组腺伴病毒的构建和鉴定

白艳霞 闫利英 马清涌 杨广笑 王全颖

西安交通大学学报(医学版)2012,Vol.33Issue(2):180-184,189,6.
西安交通大学学报(医学版)2012,Vol.33Issue(2):180-184,189,6.

介导p73去阻抑肽表达的重组腺伴病毒的构建和鉴定

Construction and identification of recombinant adeno-associated virus vector mediating the expression of the derepressing p73 peptide-p53 (N37)

白艳霞 1闫利英 1马清涌 2杨广笑 3王全颖3

作者信息

  • 1. 西安交通大学医学院第一附属医院耳鼻咽喉头颈外科
  • 2. 西安交通大学医学院第一附属医院肝胆外科,陕西西安710061
  • 3. 西安华广生物工程公司,陕西西安 710025
  • 折叠

摘要

Abstract

Objective To construct a recombinant adeno-associated virus vector mediating the expression of the derepressing p73 peptide-p53(N37) so as to lay a foundation for further research on gene therapy of malignant tumors. Methods The p53(N37) gene was obtained by self-complementary primer PCR and T-vector cloning techniques; then the p53(N37) gene and HA2-TAT segment were cloned into pUC19/NT4 vector after digested with restriction enzyme. The fusion gene of NT4-p53(N37)-HA2-TAT was subcloned into the shuttle plasmid of adeno-associated pSSHG-CMV, and recombinant plasmid pSSHG-CMV/NT4-p53 (N37)-HA2-TAT was constructed and identified by enzyme cutting analysis. The rAAV/NT4-p53 (N37 )-HA2-TAT was produced by using calcium phosphate coprecipitation method and HEK 293 cell line was co-transfected by pSSHG-CMV/NT4 -p53(N37)-HA2-TAT, aid plasmid pAAV-Ad and adenovirus genome plasmid pFG140. The virus titer was determined by dot-blot hybridization. The effect of rAAV/NT4-p53 (N37)-HA2-TAT on HepG2 cell line was measured by a methyl thiazolyl tetrazolium (MTT) assay and flow cytometry. Results The p53 (N37) gene was confirmed by restriction enzyme digestion and DNA sequencing. High titer of recombinant adeno-associated virus was obtained by homologous recombination in HEK293 cells (2×1013pfu/L). The rAAV/NT4-p53(N37)-HA2-TAT had a notable lethal effect on HepG2 cells and this effect was realized by inducing the apoptosis of HepG2 cells. Conclusion The recombinant adeno-associated virus vector mediating the expression of the derepressing p73 peptide-p53 (N37) has been successfully constructed by molecular cloning and in vitro recombination techniques in this experiment, which lays a foundation for further research on gene therapy of malignant tumors.

关键词

NT4-p53(N37)-HA2-TAT/p53(N37)/p73/重组腺伴病毒/恶性肿瘤/基因治疗

Key words

NT4-p53 (N37)-HA2-TAT/ p53(N37)/ p73/ recombinant adeno-associated virus/ malignant tumor/ gene therapy

分类

医药卫生

引用本文复制引用

白艳霞,闫利英,马清涌,杨广笑,王全颖..介导p73去阻抑肽表达的重组腺伴病毒的构建和鉴定[J].西安交通大学学报(医学版),2012,33(2):180-184,189,6.

基金项目

国家自然科学基金青年项目(No.81102056) (No.81102056)

西安交通大学医学创新基金(No.GH0203115) (No.GH0203115)

西安交通大学学报(医学版)

OA北大核心CSCDCSTPCD

1671-8259

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