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碳水化合物对代谢调节基因的转录调控

Transcriptional control of metabolic regulation genes by carbohydrates.

作者信息

Vaulont S, Kahn A

机构信息

Institut Cochin de Génétique Moléculaire, INSERM Unité 129, Paris, France.

出版信息

FASEB J. 1994 Jan;8(1):28-35. doi: 10.1096/fasebj.8.1.8299888.

Abstract

Glucose can modulate the transcription of many genes, particularly those encoding enzymes of liver metabolism. The transcriptional effect of glucose can be indirect, being mediated in vivo by hormonal variations, especially increase in insulin and decrease in glucagon secretion. Whereas the transcription of the glucokinase gene, for example, is stimulated by insulin without the aid of glucose, the transcriptional activation of most glycolytic and lipogenic genes in hepatocytes requires the presence of both glucose and insulin. The role of insulin in the activation of these genes seems mainly to stimulate glucokinase synthesis, and thus to permit glucose phosphorylation. In some cells in which hexokinase activity is constitutive, the glucose-dependent activation of the same genes does not require insulin and, in addition, can be produced by the nonmetabolisable analog, 2-deoxyglucose. In hepatocytes, the insulin effect on the glucose-dependent activation of the L-pyruvate kinase gene can be reproduced by fructose at low concentrations. Fructose probably acts through the fructose 1-phosphate dependent deinhibition of glucokinase activity. A glucose/carbohydrate element has been identified on the L-type pyruvate kinase and spot 14 gene promoters. It is able to bind, in vitro, transcriptional factors of the MLTF/USF family and could act in cooperation with tissue-specific contiguous elements, such as the HNF4 binding site in the L-type pyruvate kinase gene.

摘要

葡萄糖可调节许多基因的转录,尤其是那些编码肝脏代谢酶的基因。葡萄糖的转录作用可能是间接的,在体内由激素变化介导,特别是胰岛素增加和胰高血糖素分泌减少。例如,葡萄糖激酶基因的转录在没有葡萄糖的情况下也可被胰岛素刺激,而肝细胞中大多数糖酵解和脂肪生成基因的转录激活则需要葡萄糖和胰岛素同时存在。胰岛素在这些基因激活中的作用似乎主要是刺激葡萄糖激酶的合成,从而使葡萄糖能够磷酸化。在一些己糖激酶活性组成性存在的细胞中,相同基因的葡萄糖依赖性激活不需要胰岛素,此外,不可代谢的类似物2-脱氧葡萄糖也可产生这种激活作用。在肝细胞中,低浓度的果糖可重现胰岛素对L-丙酮酸激酶基因葡萄糖依赖性激活的作用。果糖可能通过果糖-1-磷酸依赖的方式解除对葡萄糖激酶活性的抑制作用来发挥作用。在L型丙酮酸激酶和斑点14基因启动子上已鉴定出一个葡萄糖/碳水化合物元件。它在体外能够结合MLTF/USF家族的转录因子,并可能与组织特异性的相邻元件协同作用,如L型丙酮酸激酶基因中的HNF4结合位点。

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