| Autor: |
Bardag-Gorce F; Department of Pathology, LA Biomed Research Institute, Harbor-UCLA Medical Center, 1000 W. Carson St., Torrance, CA 90509, USA., French BA, Joyce M, Baires M, Montgomery RO, Li J, French S |
| Jazyk: |
angličtina |
| Zdroj: |
Experimental and molecular pathology [Exp Mol Pathol] 2007 Apr; Vol. 82 (2), pp. 197-202. Date of Electronic Publication: 2007 Jan 08. |
| DOI: |
10.1016/j.yexmp.2006.10.006 |
| Abstrakt: |
When rats are fed ethanol intragastrically at a constant rate for 1 month, the urinary alcohol level (UAL) cycles over 7-9 day intervals. At the peak UAL, the liver is hypoxic shifting the redox state to a reduced rate. Microarray analysis done on livers at the UAL peaks shows changes in approximately 1300 gene expression compared to the pair-fed controls. To determine the mechanism of the gene expression changes, histone acetylation regulation was investigated in liver nuclear extracts at the peaks and troughs of the UAL and their pair-fed controls. No change occurred in SirT-1. P300, a histone acetyltransferase (HAT), which acetylates histone H3 on lysine 9, was increased at the peaks. Histone 3 acetylated at lysine 9 was also increased at the peaks. This indicates that the up regulated genes at the UAL peaks resulted from an increase in p300 transcription regulation, epigenetically. P300 activates transcription of numerous genes in response to signal transcription factors such as H1F 1alpha, increased in the nucleus at UAL peaks. Signal transduction pathways, such as NFkappaB, AP-1, ERK, JNK, and p38 were not increased at the peaks. beta-Catenin was increased in the nuclear extract at the UAL troughs, where increased gene expression was absent. The increase in gene expression at the peaks was due, in part, to increased acetylation of histone 3 at lysine 9. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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