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高脂饮食诱导的miR-122调节吉富罗非鱼肝中的脂质代谢和脂肪沉积。

High Fat Diet-Induced miR-122 Regulates Lipid Metabolism and Fat Deposition in Genetically Improved Farmed Tilapia (GIFT, ) Liver.

作者信息

Qiang Jun, Tao Yi Fan, Bao Jing Wen, Chen De Ju, Li Hong Xia, He Jie, Xu Pao

机构信息

Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, China.

Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, China.

出版信息

Front Physiol. 2018 Oct 5;9:1422. doi: 10.3389/fphys.2018.01422. eCollection 2018.

Abstract

The liver is an important organ for the regulation of lipid metabolism. In genetically improved farmed tilapia (GIFT, ), fat deposition in the liver occurs when they are fed high-lipid diets over a long term. This can affect their growth, meat quality, and disease resistance. MicroRNAs (miRNAs) are known to be crucial regulatory factors involved in lipid metabolism; however, the mechanism by which they regulate lipid deposition in GIFT remains unclear. Comparative miRNA expression profiling between GIFT fed a normal diet and those fed a high-lipid diet showed that miR-122 is closely related to lipid deposition. Using miR-122 as a candidate, we searched for a binding site for miR-122 in the 3'-untranslated region (UTR) of the stearoyl-CoA desaturase gene () using bioinformatics tools, and then confirmed its functionality using the luciferase reporter gene system. Then, the regulatory relationship between this miRNA and its target gene was analyzed using real-time polymerase chain reaction (qRT-PCR) and western blotting analyses. Last, we investigated the effect of the loss of miR-122 expression on lipid metabolism in GIFT. The results showed that a sequence in the 3'-UTR region of of GIFT was complementary to the miR-122 seed region, and there was a negative relationship between the expression of miRNA and expression. Inhibition of miR-122 up-regulated , increased the expression of fat synthesis-related genes, increased hepatic triglyceride and cholesterol contents, and promoted weight gain in fish. Our results showed that miR-122 targets to mediate hepatic fat metabolism. These results provide new insights for the prevention and treatment of fatty liver disease in GIFT.

摘要

肝脏是调节脂质代谢的重要器官。在遗传改良养殖罗非鱼(GIFT)中,长期投喂高脂饲料时肝脏会出现脂肪沉积。这会影响它们的生长、肉质和抗病能力。已知微小RNA(miRNA)是参与脂质代谢的关键调节因子;然而,它们在GIFT中调节脂质沉积的机制仍不清楚。对正常饮食喂养的GIFT和高脂饮食喂养的GIFT进行比较miRNA表达谱分析表明,miR-122与脂质沉积密切相关。以miR-122为候选物,我们使用生物信息学工具在硬脂酰辅酶A去饱和酶基因()的3'-非翻译区(UTR)中搜索miR-122的结合位点,然后使用荧光素酶报告基因系统确认其功能。然后,使用实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹分析来分析这种miRNA与其靶基因之间的调控关系。最后,我们研究了miR-122表达缺失对GIFT脂质代谢的影响。结果表明,GIFT的3'-UTR区域中的一个序列与miR-122种子区域互补,并且miRNA的表达与表达之间存在负相关关系。抑制miR-122会上调,增加脂肪合成相关基因的表达,增加肝脏甘油三酯和胆固醇含量,并促进鱼的体重增加。我们的结果表明,miR-122靶向以介导肝脏脂肪代谢。这些结果为GIFT脂肪肝疾病的预防和治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/6182080/d5b9dcbf8dfe/fphys-09-01422-g001.jpg

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