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油酰辅酶A是硬脂酰辅酶A去饱和酶1基因亚型的主要从头合成产物,也是哈德氏腺1-烷基-2,3-二酰甘油生物合成的底物。

Oleoyl-CoA is the major de novo product of stearoyl-CoA desaturase 1 gene isoform and substrate for the biosynthesis of the Harderian gland 1-alkyl-2,3-diacylglycerol.

作者信息

Miyazaki M, Kim H J, Man W C, Ntambi J M

机构信息

Department of Biochemistry and Nutritional Sciences, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

J Biol Chem. 2001 Oct 19;276(42):39455-61. doi: 10.1074/jbc.M106442200. Epub 2001 Aug 10.

Abstract

1-Alkyl-2,3-diacylglycerol (ADG) is a unique neutral lipid found in the eyeball-associated Harderian gland (HG) of the mouse and acts as a lubricant to facilitate eyelid movement. We found that the HG of the mice with a disruption in the gene for stearoyl-CoA desaturase 1 (SCD1) (SCD1-/-) is deficient in ADG. The amount of C20:1n-9, which is a major fatty acid of ADG, was reduced by greater than 90% despite normal elongase enzyme activity proposed to elongate it from C18:1n-9. HG from SCD1-/- mice exhibited high desaturase activity toward C16:0-CoA as substrate but had very low desaturase activity toward C18:0-CoA. Feeding diets containing high levels of oleate to the SCD1-/- mice did not increase the levels of C18:1n-9 or C20:1n-9 in the HG and failed to restore the ADG to the levels found in the HG of the wild-type mouse. De novo ADG synthesis as measured by the incorporation of [(3)H]glycerol and [(14)C]glucose was high in the SCD1+/+ mouse but was reduced by greater than 90% in the HG of SCD1-/- mouse. The deficiencies in the levels of ADG and C20:1n-9 were not compensated for by the expression of SCD2 and SCD3 isoforms in the HG of the SCD1-/- mouse. These observations demonstrate that SCD1-synthesized oleoyl-CoA is a major substrate required for the biosynthesis of normal levels of ADG and that the SCD isoforms present in the HG have different substrate specificity.

摘要

1-烷基-2,3-二酰基甘油(ADG)是一种独特的中性脂质,存在于小鼠眼球相关的哈德氏腺(HG)中,起到润滑作用以促进眼睑运动。我们发现,硬脂酰辅酶A去饱和酶1(SCD1)基因缺失的小鼠(SCD1-/-)的HG中缺乏ADG。尽管存在将C18:1n-9延长为ADG主要脂肪酸C20:1n-9的正常延长酶活性,但C20:1n-9的含量仍降低了90%以上。SCD1-/-小鼠的HG对以C16:0-CoA为底物表现出高去饱和酶活性,但对C18:0-CoA的去饱和酶活性非常低。给SCD1-/-小鼠喂食含高油酸水平的日粮,并未增加HG中C18:1n-9或C20:1n-9的水平,也未能将ADG恢复到野生型小鼠HG中的水平。通过掺入[(3)H]甘油和[(14)C]葡萄糖测定的从头合成ADG在SCD1+/+小鼠中较高,但在SCD1-/-小鼠的HG中降低了90%以上。SCD1-/-小鼠HG中ADG和C20:1n-9水平的缺陷并未因SCD2和SCD3同工型的表达而得到补偿。这些观察结果表明,SCD1合成的油酰辅酶A是正常水平ADG生物合成所需的主要底物,并且HG中存在的SCD同工型具有不同的底物特异性。

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