Gene program-specific regulation of PGC-1α activity

被引:14
作者
Schmidt, Soren F. [1 ]
Mandrup, Susanne [1 ]
机构
[1] Univ So Denmark, Dept Biochem & Mol Biol, DK-5230 Odense M, Denmark
关键词
PGC-1; alpha; gluconeogenesis; liver; S6K1; TRANSCRIPTIONAL COACTIVATOR PGC-1; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; HEPATIC GLUCONEOGENESIS; RECEPTOR-ALPHA; NUCLEAR RECEPTORS; SKELETAL-MUSCLE; MITOCHONDRIAL BIOGENESIS; GLUCOSE-METABOLISM; FASTING RESPONSE;
D O I
10.1101/gad.2076411
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Peroxisome proliferator-activated receptor gamma (PPAR gamma) coactivator 1 alpha (PGC-1 alpha) activation coordinates induction of the hepatic fasting response through coactivation of numerous transcription factors and gene programs. In the June 15, 2011, issue of Genes & Development, Lustig and colleagues (pp. 1232-1244) demonstrated that phosphorylation of PGC-1 alpha by the p70 ribosomal protein S6 kinase 1 (S6K1) specifically interfered with the interaction between PGC-1 alpha and HNF4 alpha in liver and blocked the coactivation of the gluconeogenic target genes. This demonstrates how independent fine-tuning of gene programs coregulated by the same coactivator can be obtained.
引用
收藏
页码:1453 / 1458
页数:6
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