Identification and expression of a rat fatty acid elongase involved in the biosynthesis of C18 fatty acids

被引:73
|
作者
Inagaki, K [1 ]
Aki, T [1 ]
Fukuda, Y [1 ]
Kawamoto, S [1 ]
Shigeta, S [1 ]
Ono, K [1 ]
Suzuki, O [1 ]
机构
[1] Hiroshima Univ, Grad Sch Adv Sci Matter, Dept Mol Biotechnol, Higashihiroshima 7398530, Japan
关键词
fatty acid chain elongation; liver; palmitic acid; stearic acid;
D O I
10.1271/bbb.66.613
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
A major part of the palmitic acid (C16:0) generated by fatty acid synthase is converted into stearic acid (C18:0) via carbon chain elongation. Here, we describe the cloning and expression of a rat hepatic enzyme, rELO2, responsible for the elongation of C16:0, presumably at the condensing reaction. Heterologous expression experiments in a yeast, Saccharomyces cereviside, demonstrated the elongation activity of rELO2 on C16:0 and to a lesser extent, C18:0 and fatty acids with low desaturation degree. This was distinct from that rELO1, a rat homolog of HELO1, which preferably catalyzed the elongation of mono- and polyunsaturated fatty acids of C16-C20. The Northern analysis showed that the expression of rELO2, but not rELO1, in hepatocytes was activated by the cycles of fasting and refeeding rats on a fat-free diet. Under these conditions, the rELO1 was expressed constitutively in various tissues but the rELO2 transcripts were detected predominantly in liver.
引用
收藏
页码:613 / 621
页数:9
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