Yaguchi Hiroshi, Togawa Katsuhiko, Moritani Maki, Itakura Mitsuo
Division of Genetic Information, Institute for Genome Research, University of Tokushima, Tokushima 770-8503, Japan.
Genomics. 2005 May;85(5):591-9. doi: 10.1016/j.ygeno.2005.01.006.
To identify new genetic determinants relevant to type 2 diabetes (T2D), diabetic F2 progeny were generated by intercrossing F1 mice obtained from a cross of BKS.Cg-Lepr(db)+/+m and DBA/2, and T2D-related phenotypes were measured. In the F2 population, increased susceptibility to diabetes and obesity was observed. We also detected the major quantitative trait loci (QTL) modifying the severity of diabetes on chromosome 9, where peaks of logarithm of odds (LOD) overlapped for three traits. To identify candidate genes in the QTL intervals, we combined "expression QTL" (eQTL), taking mRNA levels as quantitative traits, and "interstrain sequence variations, including cSNPs." As a result, four genes were identified from cosegregation of clinical QTL with eQTL and 13 genes were found from interstrain cSNPs as candidates in the T2D modifier QTL. Our combined approach shows the acceleration of the discovery of candidate genes in the QTL of interest, spanning several megabases.
为了鉴定与2型糖尿病(T2D)相关的新遗传决定因素,通过将从BKS.Cg-Lepr(db)+/+m与DBA/2杂交获得的F1小鼠进行杂交来产生糖尿病F2后代,并测量与T2D相关的表型。在F2群体中,观察到对糖尿病和肥胖的易感性增加。我们还在9号染色体上检测到了影响糖尿病严重程度的主要数量性状基因座(QTL),其中三个性状的优势对数(LOD)峰值重叠。为了鉴定QTL区间内的候选基因,我们将以mRNA水平作为数量性状的“表达QTL”(eQTL)与“包括cSNP在内的品系间序列变异”相结合。结果,从临床QTL与eQTL的共分离中鉴定出4个基因,从品系间cSNP中发现13个基因作为T2D修饰QTL的候选基因。我们的联合方法显示了在跨越几个兆碱基的感兴趣QTL中发现候选基因的速度加快。