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卵磷脂胆固醇酰基转移酶(LCAT)的一种DNA多态性与狒狒体内LCAT活性改变及高密度脂蛋白大小分布有关。

A DNA polymorphism for LCAT is associated with altered LCAT activity and high density lipoprotein size distributions in baboons.

作者信息

Rainwater D L, Blangero J, Hixson J E, Birnbaum S, Mott G E, VandeBerg J L

机构信息

Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78228-0147.

出版信息

Arterioscler Thromb. 1992 Jun;12(6):682-90. doi: 10.1161/01.atv.12.6.682.

DOI:10.1161/01.atv.12.6.682
PMID:1350465
Abstract

A polymorphic Pvu II site was mapped to intron 5 of LCAT, the gene encoding baboon lecithin: cholesterol acyltransferase (LCAT). In a study of 83 baboons, heterozygous baboons (Pv1/Pv2) had significantly higher LCAT enzyme activity levels than did baboons homozygous for the more common allele (Pv1/Pv1). LCAT genotype explained 6% of the total variation in LCAT enzyme activity. To test for allelic effects on cholesterol metabolism, we compared serum concentrations of high density lipoprotein (HDL) cholesterol and apolipoprotein A-I (apo A-I). We also compared distributions of cholesterol and apo A-I among three HDL size classes (HDL1, HDL2, and HDL3). All measurements were obtained for each baboon after long-term feeding of a basal diet low in cholesterol and fat and again after 7 weeks on an atherogenic diet. Heterozygous baboons had significantly lower serum levels of total cholesterol than did homozygotes. In addition, we detected significant effects of LCAT genotype on size distributions of HDL cholesterol and apo A-I on both diets but did not detect any genotype-by-diet interaction. Heterozygotes had increased amounts of cholesterol and apo A-I in HDL3 particles and lower amounts of cholesterol and apo A-I in the larger HDL size classes by comparison with homozygotes. Overall, the LCAT polymorphism explained a significant proportion of total variation in cholesterol (4-10%) and apo A-I (13%) distributions on both diets. Thus, the results indicate that the LCAT polymorphism is associated with significant differences in LCAT enzyme activity and with alterations in HDL compositions.

摘要

一个多态性的Pvu II位点被定位到编码狒狒卵磷脂胆固醇酰基转移酶(LCAT)的基因LCAT的内含子5上。在一项对83只狒狒的研究中,杂合狒狒(Pv1/Pv2)的LCAT酶活性水平显著高于更常见等位基因纯合的狒狒(Pv1/Pv1)。LCAT基因型解释了LCAT酶活性总变异的6%。为了测试等位基因对胆固醇代谢的影响,我们比较了高密度脂蛋白(HDL)胆固醇和载脂蛋白A-I(apo A-I)的血清浓度。我们还比较了胆固醇和apo A-I在三种HDL大小类别(HDL1、HDL2和HDL3)中的分布情况。在每只狒狒长期喂食低胆固醇和低脂肪的基础饮食后以及在致动脉粥样化饮食7周后,分别获取了所有测量数据。杂合狒狒的血清总胆固醇水平显著低于纯合子。此外,我们检测到LCAT基因型对两种饮食中HDL胆固醇和apo A-I的大小分布均有显著影响,但未检测到任何基因型与饮食的相互作用。与纯合子相比,杂合子在HDL3颗粒中的胆固醇和apo A-I含量增加,而在较大的HDL大小类别中的胆固醇和apo A-I含量降低。总体而言,LCAT多态性解释了两种饮食中胆固醇(4 - 10%)和apo A-I(13%)分布总变异的很大一部分。因此,结果表明LCAT多态性与LCAT酶活性的显著差异以及HDL组成的改变有关。

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