Reed Danielle R, Li Xia, McDaniel Amanda H, Lu Ke, Li Shanru, Tordoff Michael G, Price R Arlen, Bachmanov Alexander A
Monell Chemical Senses Center, 3500 Market Street, Philadelphia, Pennsylvania 19104, USA.
Mamm Genome. 2003 May;14(5):302-13. doi: 10.1007/s00335-002-2170-y.
Mice have proved to be a powerful model organism for understanding obesity in humans. Single gene mutants and genetically modified mice have been used to identify obesity genes, and the discovery of loci for polygenic forms of obesity in the mouse is an important next step. To pursue this goal, the inbred mouse strains 129P3/J (129) and C57BL/6ByJ (B6), which differ in body weight, body length, and adiposity, were used in an F2 cross to identify loci affecting these phenotypes. Linkages were determined in a two-phase process. In the first phase, 169 randomly selected F2 mice were genotyped for 134 markers that covered all autosomes and the X Chromosome (Chr). Significant linkages were found for body weight and body length on Chr 2. In addition, we detected several suggestive linkages on Chr 2 (adiposity), 9 (body weight, body length, and adiposity), and 16 (adiposity), as well as two suggestive sex-dependent linkages for body length on Chrs 4 and 9. In the second phase, 288 additional F2 mice were genotyped for markers near these regions of linkage. In the combined set of 457 F2 mice, six significant linkages were found: Chr 2 (Bwq5, body weight and Bdln3, body length), Chr 4 (Bdln6, body length, males only), Chr 9 (Bwq6, body weight and Adip5, adiposity), and Chr 16 (Adip9, adiposity), as well as several suggestive linkages (Adip2, adiposity on Chr 2, Bdln4 and Bdln5, body length on Chr 9). In addition, there was a suggestive linkage to body length in males on Chr 9 (Bdln4). For adiposity, there was evidence for epistatic interactions between loci on Chr 9 (Adip5) and 16 (Adip9). These results reinforce the concept that obesity is a complex trait. Genetic loci and their interactions, in conjunction with sex, age, and diet, determine body size and adiposity in mice.
事实证明,小鼠是了解人类肥胖问题的一种强大的模式生物。单基因突变体和基因改造小鼠已被用于识别肥胖基因,而在小鼠中发现多基因形式肥胖的基因座是接下来重要的一步。为了实现这一目标,将体重、体长和肥胖程度不同的近交系小鼠品系129P3/J(129)和C57BL/6ByJ(B6)用于F2杂交,以识别影响这些表型的基因座。连锁关系通过两个阶段来确定。在第一阶段,对169只随机选择的F2小鼠进行了134个标记的基因分型,这些标记覆盖了所有常染色体和X染色体(Chr)。在第2号染色体上发现了与体重和体长显著的连锁关系。此外,我们在第2号染色体(肥胖程度)、第9号染色体(体重、体长和肥胖程度)和第16号染色体(肥胖程度)上检测到了几个暗示性的连锁关系,以及在第4号和第9号染色体上两个暗示性的与体长有关的性别依赖性连锁关系。在第二阶段,对另外288只F2小鼠在这些连锁区域附近的标记进行了基因分型。在总共457只F2小鼠中,发现了六个显著的连锁关系:第2号染色体(Bwq5,体重;Bdln3,体长)、第4号染色体(Bdln6,体长,仅雄性)、第9号染色体(Bwq6,体重;Adip5,肥胖程度)和第16号染色体(Adip9,肥胖程度),以及几个暗示性的连锁关系(Adip2,第2号染色体上的肥胖程度;Bdln4和Bdln5,第9号染色体上的体长)。此外,在第9号染色体上雄性小鼠的体长存在一个暗示性的连锁关系(Bdln4)。对于肥胖程度,有证据表明第9号染色体(Adip5)和第16号染色体(Adip9)上的基因座之间存在上位性相互作用。这些结果强化了肥胖是一个复杂性状的概念。基因座及其相互作用,连同性别、年龄和饮食,决定了小鼠的体型和肥胖程度。