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在一个多因素小鼠模型中确定四个决定肥胖的染色体位点。

Identification of four chromosomal loci determining obesity in a multifactorial mouse model.

作者信息

Warden C H, Fisler J S, Shoemaker S M, Wen P Z, Svenson K L, Pace M J, Lusis A J

机构信息

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

出版信息

J Clin Invest. 1995 Apr;95(4):1545-52. doi: 10.1172/JCI117827.

Abstract

We previously described a new mouse model for multigenic obesity, designated BSB. We now report the use of a complete linkage map approach to identify loci contributing to body fat and other traits associated with obesity in this model. Four loci exhibiting linkage with body fat, or with the weights of four different fat depots, residing on mouse chromosomes 6, 7, 12, and 15, were identified and confirmed by analysis of additional BSB mice. Each of the four loci differed with respect to their effects on the percent of body fat, specific fat depots and plasma lipoproteins. The loci exhibited allele-specific, non-additive interactions. A locus for hepatic lipase activity was co-incident with the body fat and total cholesterol loci on chromosome 7, providing a possible mechanism linking plasma lipoproteins and obesity. The chromosome 7 locus affecting body fat, total cholesterol and hepatic lipase activity was isolated in congenic strains whose donor strain regions overlap with the chromosome 7 BSB locus. These results provide candidate genes and candidate loci for the analysis of human obesity.

摘要

我们之前描述了一种用于多基因肥胖的新小鼠模型,命名为BSB。我们现在报告使用完整的连锁图谱方法来鉴定该模型中导致体脂及其他与肥胖相关性状的基因座。通过对额外的BSB小鼠进行分析,鉴定并确认了四个与体脂或四个不同脂肪库重量相关的基因座,它们分别位于小鼠的6号、7号、12号和15号染色体上。这四个基因座对体脂百分比、特定脂肪库和血浆脂蛋白的影响各不相同。这些基因座表现出等位基因特异性的非加性相互作用。一个肝脂肪酶活性基因座与7号染色体上的体脂和总胆固醇基因座重合,这为血浆脂蛋白与肥胖之间的联系提供了一种可能的机制。在供体品系区域与7号染色体BSB基因座重叠的近交系中分离出了影响体脂、总胆固醇和肝脂肪酶活性的7号染色体基因座。这些结果为人类肥胖分析提供了候选基因和候选基因座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/391b/295638/4264d840fff8/jcinvest00025-0132-a.jpg

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