West D B, Waguespack J, York B, Goudey-Lefevre J, Price R A
Obesity, Diabetes and Metabolism Section, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge 70808.
Mamm Genome. 1994 Sep;5(9):546-52. doi: 10.1007/BF00354928.
We describe a new multiple gene mouse model of differential sensitivity to dietary obesity that provides a tool for dissecting the genetic basis for body composition and obesity. AKR/J and SWR/J male mice, as well as male progeny of intercrosses between these strains, were fed a high-fat diet for 12 weeks beginning at 5 weeks of age. Body weight and energy intake were assessed weekly. At the conclusion of the dietary manipulation, an adiposity index was calculated by dividing the weight of seven dissected adipose depots by the carcass weight. AKR/J mice had approximately sixfold greater adiposity than SWR/J mice. Examination of the segregation of the adiposity trait in the progeny of crosses between these strains indicates that the trait is determined by a minimum of one to four genetic loci and that there is significant dominance of the AKR/J genotype. A preliminary analysis with markers linked to the known mouse obesity genes ob, db, tub, and fat showed no linkage with these loci. However, a quantitative trait locus was found that maps distal to the db gene on Chromosome (Chr) 4. This locus has been designated dietary obese 1 or Do1.
我们描述了一种对饮食性肥胖具有不同敏感性的新型多基因小鼠模型,该模型为剖析身体组成和肥胖的遗传基础提供了一种工具。AKR/J和SWR/J雄性小鼠,以及这些品系之间杂交产生的雄性后代,从5周龄开始喂食高脂饮食12周。每周评估体重和能量摄入。在饮食干预结束时,通过将七个解剖的脂肪库的重量除以胴体重量来计算肥胖指数。AKR/J小鼠的肥胖程度比SWR/J小鼠大约高六倍。对这些品系杂交后代中肥胖性状分离情况的检查表明,该性状至少由一到四个基因位点决定,并且AKR/J基因型具有显著的显性作用。对与已知小鼠肥胖基因ob、db、tub和fat相关的标记进行的初步分析表明,与这些位点没有连锁关系。然而,发现了一个数量性状位点,它定位于4号染色体(Chr)上db基因的远端。该位点已被命名为饮食性肥胖1或Do1。