Scherneck Stephan, Vogel Heike, Nestler Matthias, Kluge Reinhart, Schürmann Annette, Joost Hans-Georg
German Institute of Human Nutrition Potsdam-Rehbrücke, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany.
Results Probl Cell Differ. 2010;52:57-68. doi: 10.1007/978-3-642-14426-4_6.
Type 2 diabetes is a polygenic disease resulting from a combination of different disease alleles reflecting obesity, insulin resistance, and hyperglycemia. Using a positional cloning strategy with different inbred strains of mice, we mapped a disease locus for obesity-associated diabetes on chromosome 4. We analyzed all genes in this region and identified distinct differences in the expression levels of the transcription factor Zfp69. The expression of this gene mediated diabetes progression in a leptin-deficient congenic mouse line. The animals developed a disease pattern of hyperglycemia, reduced gonadal fat mass, and increased plasma and liver triglycerides, resembling a potential defect in triglyceride storage . In order to elucidate the impact of the human ortholog of Zfp69 in the development of type 2 diabetes, we tested its mRNA expression in human white adipose tissue. Consistent with the mouse data, mRNA-expression was significantly higher in diabetic subjects than in unaffected controls.
2型糖尿病是一种多基因疾病,由反映肥胖、胰岛素抵抗和高血糖的不同疾病等位基因组合导致。我们采用定位克隆策略,利用不同的近交系小鼠,在4号染色体上定位了一个与肥胖相关糖尿病的疾病位点。我们分析了该区域的所有基因,并确定了转录因子Zfp69表达水平的明显差异。该基因的表达在瘦素缺陷的同源小鼠品系中介导了糖尿病进展。这些动物出现了高血糖、性腺脂肪量减少以及血浆和肝脏甘油三酯增加的疾病模式,类似于甘油三酯储存的潜在缺陷。为了阐明Zfp69的人类同源物在2型糖尿病发生中的作用,我们检测了其在人白色脂肪组织中的mRNA表达。与小鼠数据一致,糖尿病患者的mRNA表达明显高于未受影响的对照组。