3.5

CiteScore

2.3

Impact Factor
  • ISSN 1674-8301
  • CN 32-1810/R
Leijian Guan, Kaixuan Xu, Shuyang Xu, Ningning Li, Xinru Wang, Yankai Xia, Di Wu. Profiles of metabolic gene expression in the white adiposetissue, liver and hypothalamus in leptin knockout (LepΔI14/ΔI14 )rats[J]. The Journal of Biomedical Research, 2017, 31(6): 528-540. DOI: 10.7555/JBR.31.20170021
Citation: Leijian Guan, Kaixuan Xu, Shuyang Xu, Ningning Li, Xinru Wang, Yankai Xia, Di Wu. Profiles of metabolic gene expression in the white adiposetissue, liver and hypothalamus in leptin knockout (LepΔI14/ΔI14 )rats[J]. The Journal of Biomedical Research, 2017, 31(6): 528-540. DOI: 10.7555/JBR.31.20170021

Profiles of metabolic gene expression in the white adipose tissue, liver and hypothalamus in leptin knockout (LepΔI14/ΔI14 ) rats

  • Leptin deficiency is principally linked to metabolic disorders. Leptin knockout (LepΔI14/ΔI14) Sprague Dawley rats created by CRISPR/Cas9 is a new model to study metabolic disorders. We used a whole rat genome oligonucleotide microarray to obtain tissue-specific gene expression profiles of the white adipose tissue, liver and hypothalamus in LepΔI14/ΔI14 and wild-type (WT) rats. We found 1,651 differentially expressed (enriched) genes in white adipose tissue, 916 in the liver, and 306 in the hypothalamus in the LepΔI14/ΔI14 rats compared to WT. Gene ontology category and KEGG pathway analysis of the relationships among differentially expressed genes showed that these genes were represented in a variety of functional categories, including fatty acid metabolism, molecular transducers and cellular processes. The reliability of the data obtained from microarray was verified by quantitative real-time PCR on 14 representative genes. These data will contribute to a greater understanding of different metabolic disorders, such as obesity and diabetes.
  • loading

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return