Park Hee-Bok, Jacobsson Lina, Wahlberg Per, Siegel Paul B, Andersson Leif
Department of Medical Biochemistry and Microbiology, Uppsala University, Biomedical Center, Uppsala, Sweden.
Physiol Genomics. 2006 Apr 13;25(2):216-23. doi: 10.1152/physiolgenomics.00113.2005. Epub 2006 Jan 3.
The high- and low-growth lines of chickens have been developed from a single founder population by divergent selection for body weight at 56 days of age for more than 40 generations. The two lines show a ninefold difference in body weight at selection age and several interesting correlated selection responses such as altered body composition and metabolic differences. We have generated a reciprocal intercross comprising >800 F2 birds. In a previous study, we reported the detection of 13 quantitative trait loci (QTLs) affecting growth. Here we report QTLs for body composition (fat deposition, muscle development), weight of internal organs, and metabolic traits (plasma concentrations of glucose, insulin, cholesterol, glucagon, triglycerides, and IGF-I). Most of the QTLs with convincing statistical support mapped in the vicinity of growth QTLs. One of the most interesting observations was that the type of reciprocal cross had highly significant effects on body weight at hatch and on plasma concentrations of glucose, cholesterol, insulin, and IGF-I, but it had no significant effect on body weight at 56 days of age. The reciprocal cross explained between 15 and 35% of the phenotypic variance for weight at hatch and for plasma concentrations of glucose and insulin. The observed pattern indicated that these effects were caused by maternal effects or by genetic differences in mitochondrial DNA.
通过对56日龄体重进行超过40代的分化选择,从单一的基础群体中培育出了高生长和低生长品系的鸡。这两个品系在选择年龄时体重相差9倍,并且出现了一些有趣的相关选择反应,如身体组成的改变和代谢差异。我们构建了一个包含800多只F2代鸡的正反交群体。在之前的一项研究中,我们报告了检测到13个影响生长的数量性状位点(QTL)。在此,我们报告了影响身体组成(脂肪沉积、肌肉发育)、内脏器官重量和代谢性状(血浆葡萄糖、胰岛素、胆固醇、胰高血糖素、甘油三酯和IGF-I浓度)的QTL。大多数具有令人信服的统计支持的QTL位于生长QTL附近。最有趣的观察结果之一是,正反交类型对孵化时的体重以及血浆葡萄糖、胆固醇、胰岛素和IGF-I浓度有极显著影响,但对56日龄时的体重没有显著影响。正反交解释了孵化时体重以及血浆葡萄糖和胰岛素浓度表型变异的15%至35%。观察到的模式表明,这些影响是由母体效应或线粒体DNA的遗传差异引起的。