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MicroRNA-33 regulates sterol regulatory element-binding protein 1 expression in mice

机译:MicroRNA-33调节小鼠中的固醇调节元件结合蛋白1表达

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摘要

MicroRNAs (miRs) are small non-protein-coding RNAs that bind to specific mRNAs and inhibit translation or promote mRNA degradation. Recent reports have indicated that miR-33, which is located within the intron of sterol regulatory element-binding protein (SREBP) 2, controls cholesterol homoeostasis and may be a potential therapeutic target for the treatment of atherosclerosis. Here we show that deletion of miR-33 results in marked worsening of high-fat diet-induced obesity and liver steatosis. Using miR-33−/−Srebf1+/− mice, we demonstrate that SREBP-1 is a target of miR-33 and that the mechanisms leading to obesity and liver steatosis in miR-33−/− mice involve enhanced expression of SREBP-1. These results elucidate a novel interaction between SREBP-1 and SREBP-2 mediated by miR-33 in vivo.
机译:微小RNA(miR)是小的非蛋白质RNA,与特定的mRNA结合并抑制翻译或促进mRNA降解。最近的报道表明,位于固醇调节元件结合蛋白(SREBP)2内含子内的miR-33控制胆固醇的稳态,并且可能是治疗动脉粥样硬化的潜在治疗靶标。在这里,我们显示删除miR-33会导致高脂饮食诱发的肥胖和肝脂肪变性明显恶化。使用miR-33 -/- Srebf1 +/- 小鼠,我们证明SREBP-1是miR-33的靶标,并且其导致肥胖和肝脂肪变性的机制在miR-33 -/-小鼠中,SREBP-1的表达增强。这些结果阐明了miR-33在体内介导的SREBP-1和SREBP-2之间的新型相互作用。

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