The Asparaginyl Hydroxylase Factor Inhibiting HIF-1α Is an Essential Regulator of Metabolism

被引:203
作者
Zhang, Na [1 ]
Fu, Zhenxing [2 ]
Linke, Sarah [4 ]
Chicher, Johana [5 ]
Gorman, Jeffrey J. [5 ]
Visk, DeeAnn [3 ]
Haddad, Gabriel G. [3 ]
Poellinger, Lorenz [6 ]
Peet, Daniel J. [4 ]
Powell, Frank [2 ]
Johnson, Randall S. [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Mol Biol Sect, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, Sch Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Pediat, Sch Med, La Jolla, CA 92093 USA
[4] Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA 5005, Australia
[5] PO Royal Brisbane Hosp, Queensland Inst Med Res, Prot Discovery Ctr, Brisbane, Qld 4029, Australia
[6] Karolinska Inst, S-17177 Stockholm, Sweden
关键词
HYPOXIA-INDUCIBLE-FACTOR; ANKYRIN REPEAT DOMAIN; CAROTID-BODY; FACTOR FIH; TRANSCRIPTIONAL ACTIVITY; VENTILATORY RESPONSES; IN-VIVO; OXYGEN; MICE; HIF-1;
D O I
10.1016/j.cmet.2010.03.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Factor inhibiting HIF-1 alpha (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.
引用
收藏
页码:364 / 378
页数:15
相关论文
共 37 条
[1]   Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism [J].
Aragones, Julian ;
Schneider, Martin ;
Van Geyte, Katie ;
Fraisl, Peter ;
Dresselaers, Tom ;
Mazzone, Massimiliano ;
Dirkx, Ruud ;
Zacchigna, Serena ;
Lemieux, Helene ;
Jeoung, Nam Ho ;
Lambrechts, Diether ;
Bishop, Tammie ;
Lafuste, Peggy ;
Diez-Juan, Antonio ;
Harten, Sarah K. ;
Van Noten, Pieter ;
De Bock, Katrien ;
Willam, Carsten ;
Tjwa, Marc ;
Grosfeld, Alexandra ;
Navet, Rachel ;
Moons, Lieve ;
Vandendriessche, Thierry ;
Deroose, Christophe ;
Wijeyekoon, Bhathiya ;
Nuyts, Johan ;
Jordan, Benedicte ;
Silasi-Mansat, Robert ;
Lupu, Florea ;
Dewerchin, Mieke ;
Pugh, Chris ;
Salmon, Phil ;
Mortelmans, Luc ;
Gallez, Bernard ;
Gorus, Frans ;
Buyse, Johan ;
Sluse, Francis ;
Harris, Robert A. ;
Gnaiger, Erich ;
Hespel, Peter ;
Van Hecke, Paul ;
Schuit, Frans ;
Van Veldhoven, Paul ;
Ratcliffe, Peter ;
Baes, Myriam ;
Maxwell, Patrick ;
Carmeliet, Peter .
NATURE GENETICS, 2008, 40 (02) :170-180
[2]   Oxygen Sensors at the Crossroad of Metabolism [J].
Aragones, Julian ;
Fraisl, Peter ;
Baes, Myriam ;
Carmeliet, Peter .
CELL METABOLISM, 2009, 9 (01) :11-22
[3]   The inhibition of factor inhibiting hypoxia-inducible factor (FIH) by β-oxocarboxylic acids [J].
Banerji, B ;
Garcia, AC ;
McNeill, LA ;
McDonough, MA ;
Buck, MRG ;
Hewitson, KS ;
Oldham, NJ ;
Schofield, CJ .
CHEMICAL COMMUNICATIONS, 2005, (43) :5438-5440
[4]   Abnormal sympathoadrenal development and systemic hypotension in PHD3-/- mice [J].
Bishop, Tammie ;
Gallagher, Denis ;
Pascual, Alberto ;
Lygate, Craig A. ;
de Bono, Joseph P. ;
Nicholls, Lynn G. ;
Ortega-Saenz, Patricia ;
Oster, Henrik ;
Wijeyekoon, Bhathiya ;
Sutherland, Andrew I. ;
Grosfeld, Alexandra ;
Aragones, Julian ;
Schneider, Martin ;
van Geyte, Katie ;
Teixeira, Dania ;
Diez-Juan, Antonio ;
Lopez-Barneo, Jose ;
Channon, Keith M. ;
Maxwell, Patrick H. ;
Pugh, Christopher W. ;
Davies, Alun M. ;
Carmeliet, Peter ;
Ratcliffe, Peter J. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (10) :3386-3400
[5]   Epidermal sensing of oxygen is essential for systemic hypoxic response [J].
Boutin, Adam T. ;
Weidemann, Alexander ;
Fu, Zhenxing ;
Mesropian, Lernik ;
Gradin, Katarina ;
Jamora, Colin ;
Wiesener, Michael ;
Eckardt, Kai-Uwe ;
Koch, Cameron J. ;
Ellies, Lesley G. ;
Haddad, Gabriel ;
Haase, Volker H. ;
Simon, M. Celeste ;
Poellinger, Lorenz ;
Powell, Frank L. ;
Johnson, Randall S. .
CELL, 2008, 133 (02) :223-234
[6]   Posttranslational hydroxylation of ankyrin repeats in IκB proteins by the hypoxia-inducible factor (HIF) asparaginyl hydroxylase, factor inhibiting HIF (FIH) [J].
Cockman, Matthew E. ;
Lancaster, David E. ;
Stolze, Ineke P. ;
Hewitson, Kirsty S. ;
McDonough, Michael A. ;
Coleman, Mathew L. ;
Coles, Charlotte H. ;
Yu, Xiaohong ;
Hay, Ronald T. ;
Ley, Steven C. ;
Pugh, Christopher W. ;
Oldham, Neil J. ;
Masson, Norma ;
Schofield, Christopher J. ;
Ratcliffe, Peter J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (40) :14767-14772
[7]   Proteomics-based Identification of Novel Factor Inhibiting Hypoxia-inducible Factor (FIH) Substrates Indicates Widespread Asparaginyl Hydroxylation of Ankyrin Repeat Domain-containing Proteins [J].
Cockman, Matthew E. ;
Webb, James D. ;
Kramer, Holger B. ;
Kessler, Benedikt M. ;
Ratcliffe, Peter J. .
MOLECULAR & CELLULAR PROTEOMICS, 2009, 8 (03) :535-546
[8]   Signalling Cross Talk of the HIF System: Involvement of the FIH Protein [J].
Coleman, M. L. ;
Ratcliffe, P. J. .
CURRENT PHARMACEUTICAL DESIGN, 2009, 15 (33) :3904-3907
[9]   Asparaginyl hydroxylation of the notch ankyrin repeat domain by factor inhibiting hypoxia-inducible factor [J].
Coleman, Mathew L. ;
McDonough, Michael A. ;
Hewitson, Kirsty S. ;
Coles, Charlotte ;
Mecinovic, Jasmin ;
Edelmann, Mariola ;
Cook, Kristina M. ;
Cockman, Matthew E. ;
Lancaster, David E. ;
Kessler, Benedikt M. ;
Oldham, Neil J. ;
Ratcliffe, Peter J. ;
Schofield, Christopher J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (33) :24027-24038
[10]   ASB4 is a Hydroxylation substrate of FIH and promotes vascular differentiation via an oxygen-dependent mechanism [J].
Ferguson, James E., III ;
Wu, Yaxu ;
Smith, Kevin ;
Charles, Peter ;
Powers, Kyle ;
Wang, Hong ;
Patterson, Cam .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (18) :6407-6419