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Effects of dietary carbohydrate sources on lipid metabolism and SUMOylation modification in the liver tissues of yellow catfish

机译:膳食碳水化合物来源对黄鲶肝组织脂代谢及雄性改性的影响

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Dysregulation in hepatic lipid synthesis by excess dietary carbohydrate intake is often relevant with the occurrence of fatty liver; therefore, the thorough understanding of the regulation of lipid deposition and metabolism seems crucial to search for potential regulatory targets. In the present study, we examined TAG accumulation, lipid metabolism-related gene expression, the enzyme activities of lipogenesis-related enzymes, the protein levels of transcription factors or genes involving lipogenesis in the livers of yellow catfish fed five dietary carbohydrate sources, such as glucose, maize starch, sucrose, potato starch and dextrin, respectively. Generally speaking, compared with other carbohydrate sources, dietary glucose promoted TAG accumulation, up-regulated lipogenic enzyme activities and gene expressions, and down-regulated mRNA expression of genes involved in lipolysis and small ubiquitin-related modifier (SUMO) modification pathways. Further studies found that sterol regulatory element binding protein 1 (SREBP1), a key transcriptional factor relevant to lipogenic regulation, was modified by SUMO1. Mutational analyses found two important sites for SUMOylation modification (K254R and K264R) in SREBP1. Mutant SREBP lacking lysine 264 up-regulated the transactivation capacity on an SREBP-responsive promoter. Glucose reduced the SUMOylation level of SREBP1 and promoted the protein expression of SREBP1 and its target gene stearoyl-CoA desaturase 1 (SCD1), indicating that SUMOylation of SREBP1 mediated glucose-induced hepatic lipid metabolism. Our study elucidated the molecular mechanism of dietary glucose increasing hepatic lipid deposition and found that the SREBP-dependent transactivation was regulated by SUMO1 modification, which served as a new target for the transcriptional programmes governing lipid metabolism.
机译:过量摄入碳水化合物导致的肝脏脂质合成失调通常与脂肪肝的发生有关;因此,彻底了解脂质沉积和代谢的调节对于寻找潜在的调节靶点至关重要。在本研究中,我们检测了分别饲喂葡萄糖、玉米淀粉、蔗糖、马铃薯淀粉和糊精等五种膳食碳水化合物源的黄鲶肝脏中TAG积累、脂质代谢相关基因表达、脂肪生成相关酶的酶活性、转录因子或脂肪生成相关基因的蛋白质水平。总的来说,与其他碳水化合物来源相比,膳食葡萄糖促进TAG积累,上调脂肪生成酶活性和基因表达,下调参与脂肪分解和小泛素相关修饰物(SUMO)修饰途径的基因的mRNA表达。进一步的研究发现,与脂肪生成调节相关的关键转录因子甾醇调节元件结合蛋白1(SREBP1)被SUMO1修饰。突变分析发现SREBP1中有两个重要的苏甲酰化修饰位点(K254R和K264R)。缺乏赖氨酸264的突变体SREBP上调SREBP反应启动子的反式激活能力。葡萄糖降低了SREBP1的磺酰化水平,促进了SREBP1及其靶基因硬脂酰辅酶A去饱和酶1(SCD1)的蛋白表达,表明SREBP1的磺酰化介导了葡萄糖诱导的肝脏脂质代谢。我们的研究阐明了膳食葡萄糖增加肝脏脂质沉积的分子机制,并发现SREBP依赖的反式激活受SUMO1修饰的调节,SUMO1修饰是调控脂质代谢的转录程序的新靶点。

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