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Publication : Ndrg2 is a PGC-1α/ERRα target gene that controls protein synthesis and expression of contractile-type genes in C2C12 myotubes.

First Author  Foletta VC Year  2013
Journal  Biochim Biophys Acta Volume  1833
Issue  12 Pages  3112-3123
PubMed ID  24008097 Mgi Jnum  J:204087
Mgi Id  MGI:5529572 Doi  10.1016/j.bbamcr.2013.08.011
Citation  Foletta VC, et al. (2013) Ndrg2 is a PGC-1alpha/ERRalpha target gene that controls protein synthesis and expression of contractile-type genes in C2C12 myotubes. Biochim Biophys Acta 1833(12):3112-23
abstractText  The stress-responsive, tumor suppressor N-myc downstream-regulated gene 2 (Ndrg2) is highly expressed in striated muscle. In response to anabolic and catabolic signals, Ndrg2 is suppressed and induced, respectively, in mouse C2C12 myotubes. However, little is known about the mechanisms regulating Ndrg2 expression in muscle, as well as the biological role for Ndrg2 in differentiated myotubes. Here, we show that Ndrg2 is a target of a peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha) and estrogen-related receptor alpha (ERRalpha) transcriptional program and is induced in response to endurance exercise, a physiological stress known also to increase PGC-1alpha/ERRalpha activity. Analyses of global gene and protein expression profiles in C2C12 myotubes with reduced levels of NDRG2, suggest that NDRG2 affects muscle growth, contractile properties, MAPK signaling, ion and vesicle transport and oxidative phosphorylation. Indeed, suppression of NDRG2 in myotubes increased protein synthesis and the expression of fast glycolytic myosin heavy chain isoforms, while reducing the expression of embryonic myosin Myh3, other contractile-associated genes and the MAPK p90 RSK1. Conversely, enhanced expression of NDRG2 reduced protein synthesis, and furthermore, partially blocked the increased protein synthesis rates elicited by a constitutively active form of ERRalpha. In contrast, suppressing or increasing levels of NDRG2 did not affect mRNA expression of genes involved in mitochondrial biogenesis that are regulated by PGC-1alpha or ERRalpha. This study shows that in C2C12 myotubes Ndrg2 is a novel PGC-1alpha/ERRalpha transcriptional target, which influences protein turnover and the regulation of genes involved in muscle contraction and function.
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