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在一个多因素小鼠模型中控制体脂、脂蛋白代谢和胰岛素水平的基因位点。

Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model.

作者信息

Mehrabian M, Wen P Z, Fisler J, Davis R C, Lusis A J

机构信息

Department of Medicine, University of California, Los Angeles, California 90095, USA.

出版信息

J Clin Invest. 1998 Jun 1;101(11):2485-96. doi: 10.1172/JCI1748.

Abstract

We analyzed the inheritance of body fat, leptin levels, plasma lipoprotein levels, insulin levels, and related traits in an intercross between inbred mouse strains CAST/Ei and C57BL/6J. CAST/Ei mice are unusually lean, with only approximately 8% of body weight as fat, whereas C57BL/6J mice have approximately 18% body fat. Quantitative trait locus analysis using > 200 F2 mice revealed highly significant loci (lod scores > 4.3) on chromosomes 2 (three separate loci) and 9 that contribute to mouse fat-pad mass for mice on a high-fat diet. Some loci also influenced plasma lipoprotein levels and insulin levels either on chow or high-fat diets. Two loci for body fat and lipoprotein levels (on central and distal chromosome 2) coincided with a locus having strong effects on hepatic lipase activity, an activity associated with visceral obesity and lipoprotein levels in humans. A locus contributing to plasma leptin levels (lod score 5.3) but not obesity was identified on chromosome 4, near the leptin receptor gene. These data identify candidate regions and candidate genes for studies of human obesity and diabetes, and suggest obesity is highly complex in terms of the number of genetic factors involved. Finally, they support the existence of specific genetic interactions between body fat, insulin metabolism, and lipoprotein metabolism.

摘要

我们分析了近交系小鼠CAST/Ei和C57BL/6J杂交后代中体脂、瘦素水平、血浆脂蛋白水平、胰岛素水平及相关性状的遗传情况。CAST/Ei小鼠异常消瘦,体脂仅约占体重的8%,而C57BL/6J小鼠的体脂约为18%。对200多只F2小鼠进行数量性状基因座分析发现,在高脂饮食条件下,2号染色体(三个独立基因座)和9号染色体上存在对小鼠脂肪垫质量有高度显著影响的基因座(对数优势分数>4.3)。一些基因座在正常饮食或高脂饮食条件下也会影响血浆脂蛋白水平和胰岛素水平。两个与体脂和脂蛋白水平相关的基因座(位于2号染色体中部和远端)与一个对肝脂肪酶活性有强烈影响的基因座重合,该活性与人类内脏肥胖和脂蛋白水平相关。在4号染色体上,靠近瘦素受体基因的位置发现了一个影响血浆瘦素水平(对数优势分数5.3)但不影响肥胖的基因座。这些数据确定了人类肥胖和糖尿病研究的候选区域和候选基因,并表明肥胖在涉及的遗传因素数量方面非常复杂。最后,这些数据支持了体脂、胰岛素代谢和脂蛋白代谢之间存在特定遗传相互作用的观点。

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