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碳水化合物反应元件结合蛋白(ChREBP):葡萄糖代谢和脂肪储存的关键调节因子。

Carbohydrate responsive element-binding protein (ChREBP): a key regulator of glucose metabolism and fat storage.

作者信息

Uyeda Kosaku, Yamashita Hiromi, Kawaguchi Takumi

机构信息

Department of Biochemistry, Veterans Affairs Medical Center and The University of Texas Southwestern Medical Center at Dallas, 75216, USA.

出版信息

Biochem Pharmacol. 2002 Jun 15;63(12):2075-80. doi: 10.1016/s0006-2952(02)01012-2.

DOI:10.1016/s0006-2952(02)01012-2
PMID:12110366
Abstract

Feeding a high carbohydrate diet induces transcription of more than 15 genes involved in the metabolic conversion of glucose to fat. A new transcription factor binding to a glucose response element of the pyruvate kinase and lipogenesis enzyme genes was discovered recently. This factor, termed carbohydrate responsive element-binding protein (ChREBP), is activated in response to high glucose and up-regulates these genes. Cyclic AMP and a high fat diet inhibit ChREBP and slow down glucose utilization. ChREBP is able to control transcription of lipogenic enzyme genes in response to nutritional and hormonal inputs, and may play an important role in disease states such as diabetes, obesity, and hypertension.

摘要

喂养高碳水化合物饮食会诱导超过15个参与葡萄糖代谢转化为脂肪的基因转录。最近发现了一种新的转录因子,它与丙酮酸激酶和脂肪生成酶基因的葡萄糖反应元件结合。这个因子被称为碳水化合物反应元件结合蛋白(ChREBP),它在高葡萄糖刺激下被激活,并上调这些基因。环磷酸腺苷(cAMP)和高脂肪饮食会抑制ChREBP并减缓葡萄糖利用。ChREBP能够根据营养和激素输入来控制脂肪生成酶基因的转录,并且可能在糖尿病、肥胖症和高血压等疾病状态中发挥重要作用。

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Carbohydrate responsive element-binding protein (ChREBP): a key regulator of glucose metabolism and fat storage.碳水化合物反应元件结合蛋白(ChREBP):葡萄糖代谢和脂肪储存的关键调节因子。
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Carbohydrate response element binding protein directly promotes lipogenic enzyme gene transcription.碳水化合物反应元件结合蛋白直接促进生脂酶基因转录。
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Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein.葡萄糖和环磷酸腺苷通过对碳水化合物反应元件结合蛋白的磷酸化/去磷酸化作用来调节L型丙酮酸激酶基因。
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Treatment with myo-inositol attenuates binding of the carbohydrate-responsive element-binding protein to the ChREBP-β and FASN genes in rat nonalcoholic fatty liver induced by high-fructose diet.肌醇治疗可减轻果糖诱导的大鼠非酒精性脂肪肝中碳水化合物反应元件结合蛋白与 ChREBP-β 和 FASN 基因的结合。
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Polyunsaturated fatty acids suppress glycolytic and lipogenic genes through the inhibition of ChREBP nuclear protein translocation.多不饱和脂肪酸通过抑制ChREBP核蛋白易位来抑制糖酵解和脂肪生成基因。
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ChREBP, a glucose-responsive transcriptional factor, enhances glucose metabolism to support biosynthesis in human cytomegalovirus-infected cells.ChREBP,一种葡萄糖反应性转录因子,增强葡萄糖代谢以支持人巨细胞病毒感染细胞中的生物合成。
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