Anabolic function of the type II isozyme of hexokinase in hepatic lipid synthesis

被引:21
作者
Sebastian, S
Horton, JD
Wilson, JE [1 ]
机构
[1] Michigan State Univ, Dept Biochem, E Lansing, MI 48824 USA
[2] Univ Texas, SW Med Ctr, Dept Mol Genet, Dallas, TX 75235 USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75235 USA
关键词
D O I
10.1006/bbrc.2000.2527
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
The mRNA encoding the Type II isozyme of hexokinase was markedly elevated in livers of transgenic mice overexpressing the transcriptionally active nuclear form of sterol regulatory element binding protein-1a (nSREBP-1a), but not in transgenic mice overexpressing the nSREBP-1c or nSREBP-2 isoforms. Cellulose acetate electrophoresis and immunoblotting results confirmed selective increase of the Type II isozyme in livers of transgenic mice expressing nSREBP-1a, SREBP-1a has previously been shown to activate transcription of genes encoding enzymes involved in biosynthesis of fatty acids and glycerolipids and to a lesser extent the enzymes of cholesterol biosynthesis. Thus, these results are consistent with the view that the Type II isozyme serves an anabolic function, providing precursors and reducing equivalents required for increased rates of hepatic lipid synthesis, (C) 2000 Academic Press.
引用
收藏
页码:886 / 891
页数:6
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