Ethanol increases apolipoprotein B mRNA editing in rat primary hepatocytes and McArdle cells

被引:20
作者
Van Mater, D
Sowden, MP
Cianci, J
Sparks, JD
Sparks, CE
Ballatori, N
Smith, HC [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Biochem & Biophys, Rochester, NY 14627 USA
[2] Univ Rochester, Sch Med & Dent, Dept Environm Med, Rochester, NY 14627 USA
[3] Univ Rochester, Sch Med & Dent, Dept Pathol & Lab Med, Rochester, NY 14627 USA
关键词
D O I
10.1006/bbrc.1998.9647
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apolipoprotein B (apoB) mRNA editing involves a site-specific cytidine to uridine transition catalyzed by the cytidine deaminase, APOBEC-1, in the context of and regulated by a multi-protein-containing editosome. ApoB mRNA editing in vivo is subject to tissue specific, developmental and metabolic regulation. me demonstrate for the first time that the amount of edited apoB mRNA in rat primary hepatocytes is markedly increased subsequent to transient treatment with ethanol in vitro. The apparent change in editing efficiency was dosedependent (from 0.1%-2.4% initial ethanol dose) and occurred with rapid onset. The proportion of edited apoB mRNA was also markedly enhanced in a rat hepatoma cell line, McArdle RH7777 cells and in a stable McArdle cell Line over-expressing APOBEC-1 by transient treatment with 2.5 % ethanol. in contrast, the apoB mRNA editing in a human hepatoma cell line, HepG2 cells and a stable HepG2 cell line over-expressing APOBEC-1 did not respond to ethanol treatment. The data support the possibility that editing activity is ethanol-responsive but suggest that this change is cell type-specific. (C) 1998 Academic Press.
引用
收藏
页码:334 / 339
页数:6
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