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调控型表达丙型肝炎病毒NS3/4A蛋白酶转基因小鼠的建立

孙梦宁 招明高 汪爱勤 尹文 兰海云 马玉 赵亚 吕欣 杨敬 雷迎峰 姚敏 康健

临床肝胆病杂志2011,Vol.27Issue(1):76-80,5.
临床肝胆病杂志2011,Vol.27Issue(1):76-80,5.

调控型表达丙型肝炎病毒NS3/4A蛋白酶转基因小鼠的建立

Generation of conditionally controlled transgenic mice expressing hepatitis C virus NS3/4A protease

孙梦宁 1招明高 2汪爱勤 3尹文 3兰海云 1马玉 1赵亚 1吕欣 1杨敬 1雷迎峰 1姚敏 1康健1

作者信息

  • 1. 第四军医大学基础部微生物学与病原生物学教研室,西安,710032
  • 2. 第四军医大学基础部第四军医大学药学系药理教研室,西安,710032
  • 3. 第四军医大学基础部中心实验室,西安,710032
  • 折叠

摘要

Abstract

Objective To establish conditionally regulated transgenic mice expressing nepatitis C virus (HCV) NS3 4A serine protease. Methods A recombinant plasmid PBI-Ⅲ/LoxP-Luc-PolyA-LoxP-NS3/4A was constructed by molecular cloning and transgenic mice were generated by microinjection of fertilized ovum with the larger linearized fragment obained by enzyme digesting the recombinant vector. Founder mouse and positive offsprings detected by polymerase chain reaction (PCR) were interbred with C57BL/6 mouse to establish a defined genetic background. Part of the second generations were interbred with another transgenic mouse Lap which have been stable and systematically constructed. The interbred dual transgenic offsprings previously induced with doxycycline (Dox) were detected by in vivo bioluminescent imaging (BLI). The imaging positive dual transgenics were reserved and their NS3/4A transgenic parents were interbred with C57BL/6 instead. Results Restriction analysis and sequence analysis showed that the recombinant plasmid PBI-Ⅲ/LoxP-Luc-PolyA-LoxP-NS3/4A was successfully constructed. 6 founder transgenic mouse were obtained and 3 of them have been spread to fourth generation. Trausgenic mouse stably expressing the exogenous reporter gene luciferase (Luc) were selected by BLI. Conclusion Transgenic mouse conditionally expressing HCV NS3/4A serine protease were successfully generated.

关键词

肝炎病毒属/模型,动物/小鼠,转基因

分类

医药卫生

引用本文复制引用

孙梦宁,招明高,汪爱勤,尹文,兰海云,马玉,赵亚,吕欣,杨敬,雷迎峰,姚敏,康健..调控型表达丙型肝炎病毒NS3/4A蛋白酶转基因小鼠的建立[J].临床肝胆病杂志,2011,27(1):76-80,5.

基金项目

国家"863"计划专题(2007AA02Z154) (2007AA02Z154)

国家自然科学基金(30872218) (30872218)

陕西省科技攻关计划(2010K15-03-04) (2010K15-03-04)

临床肝胆病杂志

OACSTPCD

1001-5256

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