引用本文
  • 魏飞宇,成燕,李进,等.含Ⅲ型纤连蛋白域蛋白5真核表达载体的构建及初步功能研究[J].同济大学学报(医学版),2015,36(4):19-24, 37.    [点击复制]
  • WEI Fei-yu,CHENG Yan,LI Jin,et al.Construction and preliminary functional studies of Fibronectin type Ⅲ domain-containing protein 5 eukaryotic expression vector[J].同济大学学报(医学版),2015,36(4):19-24, 37.   [点击复制]
【打印本页】 【在线阅读全文】【下载PDF全文】 查看/发表评论下载PDF阅读器关闭

←前一篇|后一篇→

过刊浏览    高级检索

本文已被:浏览 510次   下载 500 本文二维码信息
码上扫一扫!
含Ⅲ型纤连蛋白域蛋白5真核表达载体的构建及初步功能研究
魏飞宇,成燕,李进,肖俊杰,周蕾
0
(南京医科大学第一附属医院心脏内科,南京 210029;同济大学附属同济医院心身科,上海 200065;上海大学生命科学学院,上海 200444)
摘要:
目的 构建含小鼠FNDC5基因的绿色荧光蛋白表达载体pEGFP-C3-FNDC5,并初步探索其对C2C12肌细胞的线粒体能量代谢的影响。方法 应用反转录-聚合酶链反应法从小鼠腓肠肌和心脏组织中扩增出两端带有HindⅢ和EcoRⅠ酶切位点的FNDC5编码片段,经回收、纯化酶切后,依次连接到质粒PMD19-T和pEGFP-C3上,获得过表达载体后转染至C2C12肌细胞,48h后以激光共聚焦显微镜拍摄线粒体荧光强度,以荧光定量PCR检测与线粒体能量代谢相关的基因PGC-1β、ATPase6、ND1和ND6的表达情况。结果 PCR及测序结果表明:重组质粒pEGFP-C3含有FNDC5段,方向及大小正确,过表达FNDC5可以增强线粒体荧光强度,并增加线粒体能量代谢相关的基因PGC-1β、ATPase6、ND1和ND6的表达。结论 成功构建了小鼠真核表达载体pEGFP-C3-FNDC5,过表达FNDC5可以增强线粒体能量代谢。
关键词:  FNDC5基因  真核表达载体  质粒构建  线粒体  能量  小鼠
DOI:10.16118/j.1008-0392.2015.04.004
投稿时间:2015-03-17
基金项目:国家自然基金青年项目(81400885)
Construction and preliminary functional studies of Fibronectin type Ⅲ domain-containing protein 5 eukaryotic expression vector
WEI Fei-yu,CHENG Yan,LI Jin,XIAO Jun-jie,ZHOU Lei
(Dept.of Cardiology, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China;Dept.of Psychiatry, Tongji Hospital, Tongji University, Shanghai 200065, China;School of Life Science, Shanghai University, Shanghai 200444, China)
Abstract:
Objective To construct eukaryotic expression vector pEGFP-C3-FNDC5 and to investilate its role in regulating mitochondrial biogenesis in C2C12 myocytes. Methods The cDNA coding sequence of FNDC5 containing digest site HindⅢ and EcoRⅠ was amplified by RT-PCR from gastrocnemius muscle and heart tissue of mice, and was then inserted into PMD19-T vector and pEGFP-C3 vector. The recombined plasmid was identified by PCR and further sequenced. After transfection of vector for 48h, mitochondrial content was measured by confocal microscopy and genes regulating mitochondrial biogenesis was determined by quantitative Real-Time polymerase chain reaction(qRT-PCR). ResultsPCR and DNA sequencing results showed that the recombinant plasmid pEGFP-C3-FNDC5 contained the fragment of FNDC5. FNDC5 overexpression enhanced mitochondrial content and also increased the expression of PGC-1β, ATPase6, ND1 and ND6. Conclusion The eukaryotic expression vector pEGFP-C3-FNDC5 has been constructed successfully. FNDC5 overexpre-ssion can enhance mitochondrial biogenesis.
Key words:  FNDC5 gene  eukaryotic expression vector  vector construct  mitochondrial  energy  mice

您是第5095606位访问者
版权所有《同济大学学报(医学版)》编辑部
主管单位:教育部 主办单位:同济大学
地  址: 上海四平路1239号 邮编:200092 电话:021-65980705 E-mail: yxxb@tongji.edu.cn
本系统由北京勤云科技发展有限公司设计