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TALEN构建Fndc5基因敲除小鼠及初步分析

吴子环 匡世焕 金文 胡雄兵 毛凤仪 王超 张彬 庄峰锋 胡克平 孙晓波 刘晓

中国比较医学杂志2016,Vol.26Issue(6):37-41,47,6.
中国比较医学杂志2016,Vol.26Issue(6):37-41,47,6.DOI:10.3969/j.issn.1671-7856.2016.06.008

TALEN构建Fndc5基因敲除小鼠及初步分析

Constructtion of a Fndc5 knockout mouse model by TALEN-mediated DNA targeting

吴子环 1匡世焕 2金文 3胡雄兵 4毛凤仪 3王超 5张彬 3庄峰锋 6胡克平 3孙晓波 5刘晓3

作者信息

  • 1. 宁波大学海洋学院,浙江 宁波 315000
  • 2. 中国医学科学院药用植物研究所药理毒理中心中药 天然药物 创新药物研发北京市重点实验室、中国医学科学院-普渡大学脂肪代谢联合实验室,北京 100193
  • 3. 中国医学科学院药用植物研究所药理毒理中心中药 天然药物 创新药物研发北京市重点实验室、中国医学科学院-普渡大学脂肪代谢联合实验室,北京 100193
  • 4. 普渡大学动物系,美国
  • 5. 北京唯尚立德生物科技有限公司,北京 100085
  • 6. 普渡大学动物系,美国
  • 折叠

摘要

Abstract

Objective To construct Fndc5 knockout mouse models and provide animal models for related studies in the future. Methods Indels were introduced into FNIII domain of Fndc5 gene by TALEN technology in mice, and genotypes were identified by sequencing. To set stable genetic system by pairing. Then at mRNA and DNA levels identified the genetype of born mice. At the same time the body weight and blood glucose of the mice at different ages were analyzed. Finally the Fndc5 expression in the kidney, liver, brain, muscles, heart and other organs was determined by qPCR. Results Four different Fndc5⁃KO lines were generated. The body weight and blood glucose of the mice at different ages showed no significant differences. Finally high Fndc5 expressions in the muscles, heart and other organs were determined. Conclusions We Have for the first time successfully generated Fndc5 knockout ( KO ) mouse model using TALEN mediated DNA targeting technique, and performed preliminary analysis. This Fndc5 knockout ( KO) mouse model provides a novel tool for further studies on the in vivo function of FNDC5.

关键词

骨骼肌/Fndc5基因/纤维连接蛋白/TALEN

Key words

Skeletal muscle/Fndc5/Fibronectin/TALEN/Knockout mouse model

分类

医药卫生

引用本文复制引用

吴子环,匡世焕,金文,胡雄兵,毛凤仪,王超,张彬,庄峰锋,胡克平,孙晓波,刘晓..TALEN构建Fndc5基因敲除小鼠及初步分析[J].中国比较医学杂志,2016,26(6):37-41,47,6.

基金项目

国家自然科学基金面上项目(81471070);“重大新药创制”科技重大专项(2012ZX09101、2012ZX09301002-001);诺华诺德-协和英才基金(肌信息素抵抗肥胖作用机理的研究);药植所创新团队发展计划资助。 ()

中国比较医学杂志

OA北大核心CSTPCD

1671-7856

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