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Foxo1 links insulin signaling to C/EBPα and regulates gluconeogenesis during liver development
Author(s) -
Sekine Keisuke,
Chen YenRong,
Kojima Nobuhiko,
Ogata Kazuhiro,
Fukamizu Akiyoshi,
Miyajima Atsushi
Publication year - 2007
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7601784
Subject(s) - foxo1 , biology , gluconeogenesis , phosphoenolpyruvate carboxykinase , transcription factor , ccaat enhancer binding proteins , endocrinology , medicine , gene , biochemistry , metabolism , dna binding protein
C/EBPα is a key transcription factor indispensable for the onset of gluconeogenesis in perinatal liver. However, C/EBPα was already expressed in fetal liver, suggesting that the expression of C/EBPα alone does not account for the dramatic increase of the expression of metabolic genes, and hence an additional factor(s) is expected to function cooperatively with C/EBPα in perinatal liver. We show here that expression of Foxo1 was sharply increased in the perinatal liver and augmented C/EBPα‐dependent transcription. Foxo1 bound C/EBPα via its forkhead domain, and Foxo1 bound to the promoter of a gluconeogenic gene, phosphoenolpyruvate carboxykinase (PEPCK), in a C/EBPα‐dependent manner in vivo . Insulin inhibited the expression of PEPCK in a culture of fetal liver cells, and also the C/EBPα‐dependent transcription enhanced by Foxo1. These results indicate that Foxo1 regulates gluconeogenesis cooperatively with C/EBPα, and also links insulin signaling to C/EBPα during liver development.