CCAAT/enhancer-binding protein β is required for activation of genes for ornithine cycle enzymes by glucocorticoids and glucagon in primary-cultured hepatocytes

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• 作者：Kimura ; Tatsuya ; Chowdhury ; Shoaib ; Tanaka ; Takashi ; Shimizu ; Atsuko ; Iwase ; Katsuro ; Oyadomari ; Seiichi ; et. al.
• 关键词：Transcription factor ; Gene regulation ; Hormone ; Dexamethasone ; Gene targeting ; Knockout mouse ; CPS ; carbamylphosphate synthetase ; OTC ; ornithine transcarbamylase ; AS ; argininosuccinate synthetase ; AL ; argininosuccinate lyase ; C/EBP ; CCAAT/enhancer-binding
• 刊名：FEBS Letters
• 出版年：2001
• 出版时间：April 6, 2001
• 年：2001
• 卷：494
• 期：1-2
• 页码：105-111
• 全文大小：404 K

文摘

Transcription of genes for enzymes of the ornithine cycle is activated by hormones such as glucocorticoids and glucagon. Promoters and enhancers of several genes for the enzymes interact with the CCAAT/enhancer-binding protein (C/EBP) family of transcription factors, and C/EBPβ has been suggested to mediate glucocorticoid response of the gene for arginase, the last enzyme of the cycle. To determine the contribution of C/EBPβ to hormonal regulation of genes for ornithine cycle enzymes, we examined mice with targeted disruption of the C/EBPβ gene. Induction of genes for the enzymes by intraperitoneal injection of dexamethasone and glucagon was almost intact in the liver of C/EBPβ-deficient mice. On the other hand, in primary-cultured hepatocytes derived from C/EBPβ-deficient mice, induction of genes for the first enzyme carbamylphosphate synthetase, as well as for arginase, in response to dexamethasone and/or glucagon was severely impaired. Therefore, C/EBPβ is required for hormonal induction of the genes for ornithine cycle enzymes in primary-cultured hepatocytes, while the deficiency of C/EBPβ is compensated for in vivo.