Publications
2010
Zhang Na, Fu Zhenxing, Linke Sarah, Chicher Johana, Gorman Jeffrey J, Visk DeeAnn, Haddad Gabriel G, Poellinger Lorenz, Peet Daniel J, Powell Frank, Johnson Randall S
The asparaginyl hydroxylase factor inhibiting HIF-1alpha is an essential regulator of metabolism. Article de journal
Dans: Cell metabolism, vol. 11, non 5, p. 364–378, 2010, ISSN: 1932-7420 1550-4131 1550-4131.
Résumé | Liens | BibTeX | Étiquettes: alpha Subunit/*antagonists & inhibitors/genetics, Animals, Asparagine/genetics/metabolism, Dietary Fats/pharmacology, Fatty Liver/etiology, Glucose/metabolism, Hyperventilation/etiology, Hypoxia-Inducible Factor 1, Insulin/metabolism, Knockout, Lipid Metabolism, Mice, Mixed Function Oxygenases/deficiency/genetics/*metabolism, PPSE, Transcriptional Activation, Weight Gain
@article{zhang_asparaginyl_2010,
title = {The asparaginyl hydroxylase factor inhibiting HIF-1alpha is an essential regulator of metabolism.},
author = {Na Zhang and Zhenxing Fu and Sarah Linke and Johana Chicher and Jeffrey J Gorman and DeeAnn Visk and Gabriel G Haddad and Lorenz Poellinger and Daniel J Peet and Frank Powell and Randall S Johnson},
doi = {10.1016/j.cmet.2010.03.001},
issn = {1932-7420 1550-4131 1550-4131},
year = {2010},
date = {2010-01-01},
journal = {Cell metabolism},
volume = {11},
number = {5},
pages = {364--378},
abstract = {Factor inhibiting HIF-1alpha (FIH) is an asparaginyl hydroxylase. Hydroxylation of HIF-alpha proteins by FIH blocks association of HIFs with the transcriptional coactivators CBP/p300, thus inhibiting transcriptional activation. We have created mice with a null mutation in the FIH gene and found that it has little or no discernable role in mice in altering classical aspects of HIF function, e.g., angiogenesis, erythropoiesis, or development. Rather, it is an essential regulator of metabolism: mice lacking FIH exhibit reduced body weight, elevated metabolic rate, hyperventilation, and improved glucose and lipid homeostasis and are resistant to high-fat-diet-induced weight gain and hepatic steatosis. Neuron-specific loss of FIH phenocopied some of the major metabolic phenotypes of the global null animals: those mice have reduced body weight, increased metabolic rate, and enhanced insulin sensitivity and are also protected against high-fat-diet-induced weight gain. These results demonstrate that FIH acts to a significant degree through the nervous system to regulate metabolism.},
keywords = {alpha Subunit/*antagonists & inhibitors/genetics, Animals, Asparagine/genetics/metabolism, Dietary Fats/pharmacology, Fatty Liver/etiology, Glucose/metabolism, Hyperventilation/etiology, Hypoxia-Inducible Factor 1, Insulin/metabolism, Knockout, Lipid Metabolism, Mice, Mixed Function Oxygenases/deficiency/genetics/*metabolism, PPSE, Transcriptional Activation, Weight Gain},
pubstate = {published},
tppubtype = {article}
}