Regulation of phosphoenolpyruvate carboxykinase (GTP) gene

被引:613
作者
Hanson, RW [1 ]
Reshef, L [1 ]
机构
[1] HEBREW UNIV JERUSALEM, HADASSAH MED SCH, DEPT DEV BIOCHEM, IL-91010 JERUSALEM, ISRAEL
关键词
p-enolpyruvate carboxykinase; hormones; gluconeogenesis; transcription factors; development; gene knockouts;
D O I
10.1146/annurev.biochem.66.1.581
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phosphoenolpyruvate carboxykinase (GTP) (EC 4.1.1.32) (PEPCK) is a key enzyme in the synthesis of glucose in the liver and kidney and of glyceride-glycerol in white adipose tissue and the small intestine. The gene for the cytosolic form of PEPCK (PEPCK-C) is acutely regulated by a variety of dietary and hormonal signals, which result in alteration of synthesis of the enzyme. Major factors that increase PEPCK-C gene expression include cyclic AMP, glucocorticoids, and thyroid hormone, whereas insulin inhibits this process. PEPCK-C is absent in fetal liver but appears at birth, concomitant with the capacity for gluconeogenesis. Regulatory elements that control transcription of the PEPCK-C gene in liver, kidney, and adipose tissue have been delineated, and many of the transcription factors that bind to these elements have been identified. Transgenic mice have been especially useful in elucidating the physiological roles of specific sequence elements in the PEPCK-C gene promoter and in demonstrating the key role played at these sites by the isoforms of CAAT/enhancer binding protein in patterning of PEPCK-C gene expression during the perinatal period. The PEPCK-C gene provides a model for the metabolic control of gene transcription.
引用
收藏
页码:581 / 611
页数:31
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