Estrogen related receptors (ERRs): A new dawn in transcriptional control of mitochondrial gene networks

被引:153
作者
Eichner, Lillian J. [1 ,2 ]
Giguere, Vincent [1 ,2 ,3 ,4 ]
机构
[1] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3A 1A1, Canada
[4] McGill Univ, Dept Oncol, Montreal, PQ H3A 1A1, Canada
关键词
Energy metabolism; Functional genomics; Nuclear receptors; PGC-1; PROLIFERATOR-ACTIVATED RECEPTOR; PHOSPHORYLATION-DEPENDENT SUMOYLATION; BREAST-CANCER CELLS; NUCLEAR RECEPTORS; GAMMA COACTIVATOR-1-ALPHA; ENERGY-METABOLISM; RESPONSE ELEMENT; INVERSE AGONIST; SKELETAL-MUSCLE; DOWN-REGULATION;
D O I
10.1016/j.mito.2011.03.121
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial dysfunction contributes to the etiology of numerous diseases. Consequently, improving our knowledge of how to modulate mitochondrial activity is of considerable interest. One means to achieve this goal would be to control in a global and comprehensive manner the expression of most if not all nuclear encoded mitochondrial genes. The advent of genome-wide location analysis of transcription factor occupancy coupled with functional studies in cell and animal models has recently shown that three transcription factors possess this unique attribute. Unexpectedly, these factors are orphan members of the superfamily of nuclear receptors known as estrogen-related receptors (ERRs) alpha, beta and gamma. In this review, we will integrate current knowledge gathered through several functional and physiological genomic studies to provide persuasive evidence that the ERRs are indeed master regulators of mitochondrial biogenesis and function. (C) 2011 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:544 / 552
页数:9
相关论文
共 111 条
[1]   Nuclear receptors, mitochondria and lipid metabolism [J].
Alaynick, William A. .
MITOCHONDRION, 2008, 8 (04) :329-337
[2]   ERRγ directs and maintains the transition to oxidative metabolism in the postnatal heart [J].
Alaynick, William A. ;
Kondo, Richard P. ;
Xie, Wen ;
He, Weimin ;
Dufour, Catherine R. ;
Downes, Michael ;
Jonker, Johan W. ;
Giles, Wayne ;
Naviaux, Robert K. ;
Giguere, Vincent ;
Evans, Ronald M. .
CELL METABOLISM, 2007, 6 (01) :13-24
[3]   ERRγ Regulates Cardiac, Gastric, and Renal Potassium Homeostasis [J].
Alaynick, William A. ;
Way, James M. ;
Wilson, Stephanie A. ;
Benson, William G. ;
Pei, Liming ;
Downes, Michael ;
Yu, Ruth ;
Jonker, Johan W. ;
Holt, Jason A. ;
Rajpal, Deepak K. ;
Li, Hao ;
Stuart, Joan ;
McPherson, Ruth ;
Remlinger, Katja S. ;
Chang, Ching-Yi ;
McDonnell, Donald P. ;
Evans, Ronald M. ;
Billin, Andrew N. .
MOLECULAR ENDOCRINOLOGY, 2010, 24 (02) :299-309
[4]   Common polymorphisms of the PPAR-γ2 (Pro12Ala) and PGC-1α (Gly482Ser) genes are associated with the conversion from impaired glucose tolerance to type 2 diabetes in the STOP-NIDDM trial [J].
Andrulionytè, L ;
Zacharova, J ;
Chiasson, JL ;
Laakso, M .
DIABETOLOGIA, 2004, 47 (12) :2176-2184
[5]   Identification of ERRα as a specific partner of PGC-1α for the activation of PDK4 gene expression in muscle [J].
Araki, M ;
Motojima, K .
FEBS JOURNAL, 2006, 273 (08) :1669-1680
[6]   Transcriptional coactivator PGC-1α controls the energy state and contractile function of cardiac muscle [J].
Arany, Z ;
He, HM ;
Lin, JD ;
Hoyer, K ;
Handschin, C ;
Toka, O ;
Ahmad, F ;
Matsui, T ;
Chin, S ;
Wu, PH ;
Rybkin, II ;
Shelton, JM ;
Manieri, M ;
Cinti, S ;
Schoen, FJ ;
Bassel-Duby, R ;
Rosenzweig, A ;
Ingwall, JS ;
Spiegelman, BM .
CELL METABOLISM, 2005, 1 (04) :259-271
[7]  
Ariazi EA, 2002, CANCER RES, V62, P6510
[8]  
Augereau Patrick, 2006, Nucl Recept Signal, V4, pe024
[9]   PPARδ:: a dagger in the heart of the metabolic syndrome [J].
Barish, GD ;
Narkar, VA ;
Evans, RM .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (03) :590-597
[10]   Epiderma growth factor-induced signaling in breast cancer cells resufts in selective target gene activation by orphan nuclear receptor estrogen-related receptor α [J].
Barry, JB ;
Giguère, V .
CANCER RESEARCH, 2005, 65 (14) :6120-6129