TALEN构建Fndc5基因敲除小鼠及初步分析
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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。


Constructtion of a Fndc5 knockout mouse model by TALEN-mediated DNA targeting
Author:
  • WU Zi-huan

    WU Zi-huan

    School of Ocean Biology, Ningbo University, Ningbo 315000, China;Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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  • HU Xiong-bing

    HU Xiong-bing

    Beijing Viewsolid Biotech Company Ltd., Beijing 100085
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  • MAO Feng-yi

    MAO Feng-yi

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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  • WANG Chao

    WANG Chao

    Department of Animal Science, Purdue University, USA
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  • ZHANG Bin

    ZHANG Bin

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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  • ZHUANG Feng-feng

    ZHUANG Feng-feng

    Beijing Viewsolid Biotech Company Ltd., Beijing 100085
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  • HU Ke-ping

    HU Ke-ping

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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  • SUN Xiao-bo

    SUN Xiao-bo

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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  • LIU Xiao

    LIU Xiao

    School of Ocean Biology, Ningbo University, Ningbo 315000, China
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  • KUANG Shi-huan

    KUANG Shi-huan

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193;Department of Animal Science, Purdue University, USA
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  • JIN Wen

    JIN Wen

    Beijing Key Laboratory of Innovative Drug Development of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, CAMS-Purdue Associate Laboratory of Adipose Metabolism, Center of Pharmacology and Toxicology, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193
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    摘要:

    目的 通过构建Fndc5基因敲除小鼠,为后续的研究提供动物模型。方法 运用TALEN技术在Fndc5基因FNIII domain中造成缺失突变,并通过测序进行基因型鉴定。通过配对建立稳定遗传系并在mRNA和DNA水平鉴定出生小鼠基因型;对不同年龄段出生小鼠进行体重、血糖分析;通过qPCR确定Fndc5在肾脏、肝脏、大脑、肌肉、心脏等组织中的表达情况。结果 成功构建并鉴定得到4种不同的Fndc5基因敲除小鼠品系;不同年龄段出生小鼠体重、血糖未见显著性差异;确定Fndc5在肌肉、心脏等组织中高表达。结论 本实验在国际上成功构建了Fndc5基因敲除小鼠,并进行了初步分析,为深入研究Fndc5基因在体内中的功能提供了动物模型。

    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.

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

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  • 最后修改日期:2016-02-25
  • 在线发布日期: 2016-06-30
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