» Articles » PMID: 20933024

Metabolic Control of Mitochondrial Biogenesis Through the PGC-1 Family Regulatory Network

Overview
Specialties Biochemistry
Biophysics
Date 2010 Oct 12
PMID 20933024
Citations 590
Authors
Affiliations
Soon will be listed here.
Abstract

The PGC-1 family of regulated coactivators, consisting of PGC-1α, PGC-1β and PRC, plays a central role in a regulatory network governing the transcriptional control of mitochondrial biogenesis and respiratory function. These coactivators target multiple transcription factors including NRF-1, NRF-2 and the orphan nuclear hormone receptor, ERRα, among others. In addition, they themselves are the targets of coactivator and co-repressor complexes that regulate gene expression through chromatin remodeling. The expression of PGC-1 family members is modulated by extracellular signals controlling metabolism, differentiation or cell growth and in some cases their activities are known to be regulated by post-translational modification by the energy sensors, AMPK and SIRT1. Recent gene knockout and silencing studies of many members of the PGC-1 network have revealed phenotypes of wide ranging severity suggestive of complex compensatory interactions or broadly integrative functions that are not exclusive to mitochondrial biogenesis. The results point to a central role for the PGC-1 family in integrating mitochondrial biogenesis and energy production with many diverse cellular functions. This article is part of a Special Issue entitled: Mitochondria and Cardioprotection.

Citing Articles

The role of mA modification during macrophage metabolic reprogramming in human diseases and animal models.

Wang H, Xu P, Yin K, Wang S Front Immunol. 2025; 16:1521196.

PMID: 40066451 PMC: 11891544. DOI: 10.3389/fimmu.2025.1521196.


Preliminary Data on the Senolytic Effects of Ledeb. Extract Containing Agrimols for Immunosenescence in Middle-Aged Humans: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Comparison Study.

Shimizu Y, Shimodan S, Hayashida M, Yazaki M, Sakurada T, Watanabe T Nutrients. 2025; 17(4).

PMID: 40004995 PMC: 11858573. DOI: 10.3390/nu17040667.


Are Mitochondria a Potential Target for Treating β-Thalassemia?.

Pierro E, Stefano V, Migone De Amicis M, Graziadei G J Clin Med. 2025; 14(4).

PMID: 40004626 PMC: 11856739. DOI: 10.3390/jcm14041095.


Eugenol Promotes Apoptosis in Leukemia Cells via Targeting the Mitochondrial Biogenesis PPRC1 Gene.

Al-Harbi S, Alkholiwy E, Ali Ahmed S, Aljurf M, Al-Hejailan R, Aboussekhra A Cells. 2025; 14(4).

PMID: 39996733 PMC: 11853370. DOI: 10.3390/cells14040260.


Brown Adipose Tissue undergoes pathological perturbations and shapes C2C12 myoblast homeostasis in the SOD1-G93A mouse model of Amyotrophic Lateral Sclerosis.

Rosina M, Scaricamazza S, Riggio F, Fenili G, Giannessi F, Matteocci A Heliyon. 2025; 11(3):e41801.

PMID: 39916853 PMC: 11800085. DOI: 10.1016/j.heliyon.2025.e41801.


References
1.
Becker T, Gebert M, Pfanner N, van der Laan M . Biogenesis of mitochondrial membrane proteins. Curr Opin Cell Biol. 2009; 21(4):484-93. DOI: 10.1016/j.ceb.2009.04.002. View

2.
Seelan R, Grossman L . Structural organization and promoter analysis of the bovine cytochrome c oxidase subunit VIIc gene. A functional role for YY1. J Biol Chem. 1997; 272(15):10175-81. DOI: 10.1074/jbc.272.15.10175. View

3.
Goto H, Motomura S, Wilson A, Freiman R, Nakabeppu Y, Fukushima K . A single-point mutation in HCF causes temperature-sensitive cell-cycle arrest and disrupts VP16 function. Genes Dev. 1997; 11(6):726-37. DOI: 10.1101/gad.11.6.726. View

4.
Arany Z, He H, Lin J, Hoyer K, Handschin C, Toka O . Transcriptional coactivator PGC-1 alpha controls the energy state and contractile function of cardiac muscle. Cell Metab. 2005; 1(4):259-71. DOI: 10.1016/j.cmet.2005.03.002. View

5.
HATEFI Y . The mitochondrial electron transport and oxidative phosphorylation system. Annu Rev Biochem. 1985; 54:1015-69. DOI: 10.1146/annurev.bi.54.070185.005055. View