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

机译:瘦素敲除(LepΔI14/ΔI14)大鼠的白色脂肪组织肝脏和下丘脑中的代谢基因表达谱

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摘要

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 inLepΔI14/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 theLepΔI14/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.
机译:瘦素缺乏症主要与代谢紊乱有关。瘦素敲除(Lep ΔI14/ΔI14)CRISPR / Cas9创建的Sprague Dawley大鼠是研究代谢异常的新模型。我们使用完整的大鼠基因组寡核苷酸微阵列,获得了Lep ΔI14/ΔI14和野生型(WT)大鼠中白色脂肪组织,肝脏和下丘脑的组织特异性基因表达谱。与WT相比,在Lep ΔI14/ΔI14大鼠中,我们在白色脂肪组织中发现了1651个差异表达(富集)的基因,在肝脏中表达916个,在下丘脑中表达了306个。基因本体分类和KEGG通路对差异表达基因之间关系的分析表明,这些基因代表了多种功能类别,包括脂肪酸代谢,分子传感器和细胞过程。通过对14个代表性基因进行实时定量PCR验证了从微阵列获得的数据的可靠性。这些数据将有助于更好地了解不同的代谢疾病,例如肥胖症和糖尿病。

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