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Diet-dependent alterations of hepatic scd1 expression are accompanied by differences in promoter methylation

机译:饮食依赖性肝scd1表达的改变伴随启动子甲基化的差异

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Obesity and alterations of lipid homeostasis are hallmarks of the metabolic syndrome and largely influenced by the dietary conditions of the individual. Although heritability is considered to be a major risk factor, the almost 40 candidate genes identified by genome-wide association studies (GWAS) so far account for only 5-10% of the observed variance in BMI in human subjects. Alternatively, diet-induced changes of epigenetic gene regulation might be involved in disturbed lipid homeostasis and weight development. The aim of this study was to investigate how a high-carbohydrate diet (HCD; 70 kcal% from carbohydrates, 10 kcal% from fat) or a high-fat diet (HFD; 20 kcal% from carbohydrates, 60 kcal% from fat) affects hepatic expression of genes involved in fatty acid metabolism and if these alterations are correlated to changes in promoter methylation. Expression of stearoyl-CoA desaturase 1 (Scd1) was lower in livers from HFD-fed C57BL/6 J mice compared to HCD-fed animals and correlated inversely with the degree of DNA methylation at 2 distinct, adjacent CpG sites in the Scd1 promoter. In contrast, expression of transcription factors peroxisome proliferator activated receptor alpha and gamma (Ppara, Pparg), and sterol regulatory element binding transcription factor 1 (Srebf1) was not affected. The degree of hepatic Scd1 promoter methylation at these CpG sites correlated positively to fat mass and serum leptin levels, whereas serum ghrelin levels were inversely correlated with methylation at both CpG sites. Taken together, hepatic expression of Scd1 is differentially affected by carbohydrate- and lipid content of the diet. These differences in Scd1 expression are associated with altered promoter methylation, indicating that diets affect lipid metabolism in the liver via epigenetic mechanisms.
机译:肥胖和脂质体内平衡的改变是代谢综合征的标志,并且在很大程度上受个体饮食条件的影响。尽管遗传力被认为是主要的危险因素,但迄今为止,全基因组关联研究(GWAS)鉴定出的近40个候选基因仅占人类受试者BMI观察到的变异的5-10%。另外,饮食引起的表观遗传基因调节的变化可能与脂质稳态和体重发展受阻有关。这项研究的目的是研究高碳水化合物饮食(HCD;碳水化合物70 kcal%,脂肪10 kcal%)或高脂饮食(HFD;碳水化合物20 kcal%,脂肪60 kcal)影响脂肪酸代谢相关基因的肝表达,如果这些改变与启动子甲基化的改变相关。与HCD喂养的动物相比,HFD喂养的C57BL / 6 J小鼠的肝脏中硬脂酰辅酶A去饱和酶1(Scd1)的表达较低,并且与Scd1启动子中两个不同的相邻CpG位点的DNA甲基化程度呈负相关。相反,转录因子过氧化物酶体增殖物激活的受体α和γ(Ppara,Pparg)和固醇调节元件结合转录因子1(Srebf1)的表达不受影响。在这些CpG位点的肝Scd1启动子甲基化程度与脂肪量和血清瘦素水平呈正相关,而在两个CpG位点,血清生长素释放肽水平与甲基化呈负相关。综上所述,饮食中的碳水化合物和脂质含量会差异性地影响Scd1的肝表达。 Scd1表达的这些差异与启动子甲基化的改变有关,表明饮食通过表观遗传机制影响肝脏中的脂质代谢。

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