Gauguier D, Froguel P, Parent V, Bernard C, Bihoreau M T, Portha B, James M R, Penicaud L, Lathrop M, Ktorza A
Wellcome Trust Centre for Human Genetics, Headington, Oxford, UK.
Nat Genet. 1996 Jan;12(1):38-43. doi: 10.1038/ng0196-38.
Goto-Kakizaki (GK) rats are a well characterized model for non-insulin dependent diabetes mellitus (NIDDM). We have used a combination of physiological and genetic studies to identify quantitative trait loci (QTLs) responsible for the control of glucose homeostasis and insulin secretion in a F2 cohort bred from spontaneously diabetic GK rats. The genetic dissection of NIDDM allowed us to map up to six independently segregating loci predisposing to hyperglycaemia, glucose intolerance or altered insulin secretion, and a seventh locus implicated in body weight. QTLs implicated in glucose tolerance and adiposity map to the same region of rat chromosome 1, and may indicate the influence of a single locus. Our study demonstrates that distinct combinations of genetic loci are responsible for different physiological characteristics associated with the diabetic phenotype in the GK rat, and it constitutes an important step for directing the search for the genetic factors involved in human NIDDM.
Goto-Kakizaki(GK)大鼠是一种特征明确的非胰岛素依赖型糖尿病(NIDDM)模型。我们结合生理学和遗传学研究,在由自发性糖尿病GK大鼠培育的F2群体中,鉴定出负责控制葡萄糖稳态和胰岛素分泌的数量性状基因座(QTL)。对NIDDM的基因剖析使我们能够定位多达六个独立分离的易导致高血糖、葡萄糖不耐受或胰岛素分泌改变的基因座,以及第七个与体重相关的基因座。与葡萄糖耐量和肥胖相关的QTL定位于大鼠1号染色体的同一区域,这可能表明存在单个基因座的影响。我们的研究表明,不同的基因座组合导致了GK大鼠糖尿病表型相关的不同生理特征,这是指导寻找人类NIDDM相关遗传因素的重要一步。