TY - JOUR
T1 - Growth hormone corrects proliferation and transcription of phosphoenolpyruvate carboxykinase in livers of old mice via elimination of CCAAT/enhancer-binding protein α-Brm complex
AU - Wang, Guo Li
AU - Shi, Xiurong
AU - Salisbury, Elizabeth
AU - Sun, Yuxiang
AU - Albrecht, Jeffrey H.
AU - Smith, Roy G.
AU - Timchenko, Nikolai A.
PY - 2007/1/12
Y1 - 2007/1/12
N2 - Growth hormone (GH), which is reduced with age, corrects the impaired proliferative capacity of livers of old animals. In this paper, we present a mechanism by which GH eliminates age-dependent negative control of proliferation and increases transcription of liver-specific genes in livers of old mice. The reduced proliferative capacities of the liver of old animals are associated with the CCAAT/enhancer-binding protein α (C/EBPα)-Brm complex, which inhibits E2F-dependent promoters. We found that a sequestration of C/EBPα into complexes with Brm leads to a weak interaction of C/EBPα with promoters of liver-specific genes, expression of which is reduced in old animals. Injection of either GH or the regulator of the amplitude of endogenous GH release, ghrelin, reduces the C/EBPα-Brm complex in livers of old mice, leading to a derepression of E2F targets, to increased interactions of C/EBPα with promoters of liver-specific genes, and to correction of their expression. GH-dependent elimination of the complex is mediated by the inhibition of cyclin D3-CDK4 activity and by elevation of a phosphatase, protein phosphatase 2A, which dephosphorylates C/EBPα and dissociates the complex.
AB - Growth hormone (GH), which is reduced with age, corrects the impaired proliferative capacity of livers of old animals. In this paper, we present a mechanism by which GH eliminates age-dependent negative control of proliferation and increases transcription of liver-specific genes in livers of old mice. The reduced proliferative capacities of the liver of old animals are associated with the CCAAT/enhancer-binding protein α (C/EBPα)-Brm complex, which inhibits E2F-dependent promoters. We found that a sequestration of C/EBPα into complexes with Brm leads to a weak interaction of C/EBPα with promoters of liver-specific genes, expression of which is reduced in old animals. Injection of either GH or the regulator of the amplitude of endogenous GH release, ghrelin, reduces the C/EBPα-Brm complex in livers of old mice, leading to a derepression of E2F targets, to increased interactions of C/EBPα with promoters of liver-specific genes, and to correction of their expression. GH-dependent elimination of the complex is mediated by the inhibition of cyclin D3-CDK4 activity and by elevation of a phosphatase, protein phosphatase 2A, which dephosphorylates C/EBPα and dissociates the complex.
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U2 - 10.1074/jbc.M608226200
DO - 10.1074/jbc.M608226200
M3 - Article
C2 - 17107955
AN - SCOPUS:33847716727
SN - 0021-9258
VL - 282
SP - 1468
EP - 1478
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 2
ER -