Gohda Tomohito, Makita Yuichiro, Shike Toshihide, Tanimoto Mitsuo, Funabiki Kazuhiko, Horikoshi Satoshi, Tomino Yasuhiko
Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Diabetes. 2003 Aug;52(8):2175-81. doi: 10.2337/diabetes.52.8.2175.
The KK/Ta strain serves as a suitable polygenic mouse model for the common form of type 2 diabetes associated with obesity in humans. Recently, we reported the susceptibility loci contributing to type 2 diabetes and related phenotypes in KK/Ta mice. In this study, we focused on expression in the kidneys and liver of KK/Ta and BALB/c mice using differential display (DD) PCR. Zn-alpha(2) glycoprotein-1 (Azgp1) mRNA levels were increased in the kidneys and liver in KK/Ta mice, and sequence analysis revealed a missense mutation. We analyzed the relationship between this polymorphism and various phenotypes in 208 KK/Ta x (BALB/c x KK/Ta) F1 backcross mice. Statistical analysis revealed that Azgp1 and D17Mit218 exhibit a suggestive linkage to body weight (8 weeks) (logarithm of odds 2.3 and 2.9, respectively). Moderate gene-gene interactions were observed at these loci. Adiponectin mRNA levels in 3T3-L1 cells transfected with the expression pcDNA 3.1 vector containing Azgp1 coding sequence of KK/Ta mice were significantly higher than those of BALB/c mice. These results suggest that Azgp1 is a possible candidate gene for regulation of body weight, elucidation of polygenic inheritance, and age-dependent changes in the genetic control of obesity.
KK/Ta品系是一种适用于人类常见的与肥胖相关的2型糖尿病的多基因小鼠模型。最近,我们报道了KK/Ta小鼠中导致2型糖尿病及相关表型的易感基因座。在本研究中,我们使用差异显示(DD)PCR技术聚焦于KK/Ta和BALB/c小鼠肾脏和肝脏中的基因表达。在KK/Ta小鼠的肾脏和肝脏中,锌-α(2)糖蛋白-1(Azgp1)的mRNA水平升高,序列分析显示存在一个错义突变。我们在208只KK/Ta×(BALB/c×KK/Ta)F1回交小鼠中分析了这种多态性与各种表型之间的关系。统计分析表明,Azgp1和D17Mit218与体重(8周龄)存在提示性连锁关系(优势对数分别为2.3和2.9)。在这些基因座观察到中等程度的基因-基因相互作用。用含有KK/Ta小鼠Azgp1编码序列的表达pcDNA 3.1载体转染的3T3-L1细胞中脂联素的mRNA水平显著高于BALB/c小鼠。这些结果表明,Azgp1可能是调节体重、阐明多基因遗传以及肥胖遗传控制中年龄依赖性变化的候选基因。