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Sökning: WFRF:(Alvaro M.) > (2005-2009) > Butyrate mediates d...

Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes

Rada-Iglesias, Alvaro (författare)
Uppsala universitet,Institutionen för genetik och patologi
Enroth, Stefan (författare)
Uppsala universitet,Centrum för bioinformatik
Ameur, Adam (författare)
Uppsala universitet,Centrum för bioinformatik
visa fler...
Koch, Christoph M. (författare)
Clelland, Gayle K. (författare)
Respuela-Alonso, Patricia (författare)
Uppsala universitet,Institutionen för genetik och patologi
Wilcox, Sarah (författare)
Dovey, Oliver M. (författare)
Ellis, Peter D. (författare)
Langford, Cordelia F. (författare)
Dunham, Ian (författare)
Komorowski, Jan (författare)
Uppsala universitet,Centrum för bioinformatik
Wadelius, Claes (författare)
Uppsala universitet,Institutionen för genetik och patologi
visa färre...
 (creator_code:org_t)
2007-06-13
2007
Engelska.
Ingår i: Genome Research. - : Cold Spring Harbor Laboratory. - 1088-9051 .- 1549-5469. ; 17:6, s. 708-719
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Butyrate is a histone deacetylase inhibitor (HDACi) with anti-neoplastic properties, which theoretically reactivates epigenetically silenced genes by increasing global histone acetylation. However, recent studies indicate that a similar number or even more genes are down-regulated than up-regulated by this drug. We treated hepatocarcinoma HepG2 cells with butyrate and characterized the levels of acetylation at DNA-bound histones H3 and H4 by ChIP-chip along the ENCODE regions. In contrast to the global increases of histone acetylation, many genomic regions close to transcription start sites were deacetylated after butyrate exposure. In order to validate these findings, we found that both butyrate and trichostatin A treatment resulted in histone deacetylation at selected regions, while nucleosome loss or changes in histone H3 lysine 4 trimethylation (H3K4me3) did not occur in such locations. Furthermore, similar histone deacetylation events were observed when colon adenocarcinoma HT-29 cells were treated with butyrate. In addition, genes with deacetylated promoters were down-regulated by butyrate, and this was mediated at the transcriptional level by affecting RNA polymerase II (POLR2A) initiation/elongation. Finally, the global increase in acetylated histones was preferentially localized to the nuclear periphery, indicating that it might not be associated to euchromatin. Our results are significant for the evaluation of HDACi as anti-tumourogenic drugs, suggesting that previous models of action might need to be revised, and provides an explanation for the frequently observed repression of many genes during HDACi treatment.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

Acetylation/drug effects
Adenocarcinoma/*metabolism
Butyrates/*pharmacology
Cell Line; Tumor
Colonic Neoplasms/*metabolism
Enzyme Inhibitors/*pharmacology
Gene Expression Profiling
Gene Expression Regulation; Neoplastic/*drug effects
Histone Deacetylases/antagonists & inhibitors/metabolism
Histones/*metabolism
Humans
Neoplasm Proteins/*metabolism
Oligonucleotide Array Sequence Analysis
Protein Processing; Post-Translational/*drug effects
MEDICINE
MEDICIN
Biology
Biologi

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