SELECTIVE HYPERMETHYLATION OF TRANSCRIBED NUCLEOSOMAL DNA BY SODIUM-BUTYRATE

被引:39
作者
BOFFA, LC
MARIANI, MR
PARKER, MI
机构
[1] UNIV CAPE TOWN,SCH MED,DEPT MED BIOCHEM,MRC,CELL BIOL ATHEROSCLEROSIS RES UNIT,CAPE TOWN 7925,SOUTH AFRICA
[2] IST,IST NAZL RIC CANC,DEPT CHEM CARCINOGENESIS,I-16132 GENOA,ITALY
关键词
D O I
10.1006/excr.1994.1107
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies have shown that treatment of cultured fibroblasts with millimolar concentrations of sodium butyrate results in increased methylation of cytosine residues in DNA. In this study, active nucleosomes were fractionated from the inactive ones by organomercurial agarose column chromatography. DNA in each fraction was hydrolyzed to its constituent bases and subjected to HPLC analysis in order to determine the 5-methylcytosine content. In control cells, the active nucleosomal DNA was hypomethylated (0.97 +/- 0.27% 5-methylcytosine) when compared with the inactive DNA fraction (1.61 +/- 0.15%). This result was not unexpected since DNA hypermethylation is generally associated with gene inactivation. Treatment of cells with sodium butyrate, however, resulted in increased methylation of the active nucleosomal DNA such that it was comparable to that of the inactive fraction of control cells (1.73 +/- 0.02% 5-methylcytosine). A much smaller increase in B-methylcytosine content was detected in the inactive DNA fraction of sodium butyrate-treated cells (from 1.61 to 1.89%). Removal of the sodium butyrate followed by a chase in butyrate-free medium for up to 120 h failed to reverse the butyrate-induced hypermethylation. Reversal was achieved only after continuous culture in butyrate-free medium for 10 days. (C) 1994 Academic Press, Inc.
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页码:420 / 423
页数:4
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