Yamada T, Miyake T, Sugiura K, Narita A, Wei K, Wei S, Moralejo D H, Ogino T, Gaillard C, Sasaki Y, Matsumoto K
Laboratory of Animal Breeding and Genetics, Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto 606-8502.
Exp Anim. 2001 Apr;50(2):115-23. doi: 10.1538/expanim.50.115.
The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is an animal model for obese-type non-insulin-dependent diabetes mellitus (NIDDM) in humans. Our present investigation was designed to identify epistatic interactions influencing NIDDM by performing least squares analysis of variance of all pairs of informative markers in 160 F2 progenies bred from an intercross of OLETF and Fischer-344 rats. We identified four interactions between Nidd15/of (chromosome 7) and Nidd16/of (chromosome 14), Nidd15/of and Nidd17/of (chromosome 15), Nidd16/of and Nidd18/of (chromosome 15), and Nidd16/of and Nidd19/of (chromosome 17), which account for a total of approximately 40% of the genetic variation of entire glucose levels after glucose challenge in the F2. The Nidd16/of locus, which is involved in three of four digenic interactions, and the Nidd19/of are likely to correspond to Nidd2/of and Nidd14/of, NIDDM loci previously identified in the F2 by single-QTL model and multiple-QTL model, respectively, while Nidd15/of, Nidd17/of and Nidd18/of loci reflect novel NIDDM loci. An aberrant increase of the entire glucose level due to synergism occurs in the double OLETF homozygote genotype of Nidd15/of and Nidd16/of, and of Nidd16/of and Nidd19/of, as well as in the OLETF homozygote genotypes of Nidd15/of and Nidd16/of, respectively, combined with the heterozygote genotypes of Nidd17/of and Nidd18/of. These findings demonstrate that inter-allelic interactions are likely to be an important component of NIDDM susceptibility.
大冢长-艾氏德岛肥胖(OLETF)大鼠是人类肥胖型非胰岛素依赖型糖尿病(NIDDM)的动物模型。我们目前的研究旨在通过对由OLETF大鼠和Fischer-344大鼠杂交产生的160只F2后代中所有信息性标记对进行最小二乘方差分析,来确定影响NIDDM的上位性相互作用。我们鉴定出Nidd15/of(第7号染色体)与Nidd16/of(第14号染色体)、Nidd15/of与Nidd17/of(第15号染色体)、Nidd16/of与Nidd18/of(第15号染色体)以及Nidd16/of与Nidd19/of(第17号染色体)之间的四种相互作用,这些相互作用总共占F2代葡萄糖激发后整个血糖水平遗传变异的约40%。参与四个双基因相互作用中的三个的Nidd16/of位点和Nidd19/of位点可能分别对应于先前通过单QTL模型和多QTL模型在F2代中鉴定出的NIDDM位点Nidd2/of和Nidd14/of,而Nidd15/of、Nidd17/of和Nidd18/of位点反映了新的NIDDM位点。在Nidd15/of和Nidd1及Nidd16/of和Nidd19/of的双OLETF纯合子基因型中,以及在Nidd15/of和Nidd16/of的OLETF纯合子基因型分别与Nidd17/of和Nidd18/of的杂合子基因型组合时,由于协同作用会出现整个血糖水平的异常升高。这些发现表明等位基因间相互作用可能是NIDDM易感性的一个重要组成部分。