Alfa Ronald W, Kim Seung K
Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA Neuroscience Program, Stanford University School of Medicine, Stanford, CA 94305, USA
Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA Department of Medicine (Oncology), Stanford University School of Medicine, Stanford, CA 94305, USA
Dis Model Mech. 2016 Apr;9(4):365-76. doi: 10.1242/dmm.023887.
Mechanisms of glucose homeostasis are remarkably well conserved between the fruit flyDrosophila melanogasterand mammals. From the initial characterization of insulin signaling in the fly came the identification of downstream metabolic pathways for nutrient storage and utilization. Defects in these pathways lead to phenotypes that are analogous to diabetic states in mammals. These discoveries have stimulated interest in leveraging the fly to better understand the genetics of type 2 diabetes mellitus in humans. Type 2 diabetes results from insulin insufficiency in the context of ongoing insulin resistance. Although genetic susceptibility is thought to govern the propensity of individuals to develop type 2 diabetes mellitus under appropriate environmental conditions, many of the human genes associated with the disease in genome-wide association studies have not been functionally studied. Recent advances in the phenotyping of metabolic defects have positionedDrosophilaas an excellent model for the functional characterization of large numbers of genes associated with type 2 diabetes mellitus. Here, we examine results from studies modeling metabolic disease in the fruit fly and compare findings to proposed mechanisms for diabetic phenotypes in mammals. We provide a systematic framework for assessing the contribution of gene candidates to insulin-secretion or insulin-resistance pathways relevant to diabetes pathogenesis.
果蝇黑腹果蝇和哺乳动物之间的葡萄糖稳态机制非常保守。从果蝇胰岛素信号的初步特征中,发现了营养物质储存和利用的下游代谢途径。这些途径的缺陷会导致类似于哺乳动物糖尿病状态的表型。这些发现激发了人们利用果蝇更好地理解人类2型糖尿病遗传学的兴趣。2型糖尿病是在持续的胰岛素抵抗背景下由胰岛素不足引起的。尽管遗传易感性被认为在适当的环境条件下决定个体患2型糖尿病的倾向,但在全基因组关联研究中与该疾病相关的许多人类基因尚未进行功能研究。代谢缺陷表型分析的最新进展使果蝇成为对大量与2型糖尿病相关基因进行功能表征的优秀模型。在这里,我们研究了果蝇中代谢疾病建模研究的结果,并将这些发现与哺乳动物糖尿病表型的提出机制进行比较。我们提供了一个系统框架,用于评估候选基因对与糖尿病发病机制相关的胰岛素分泌或胰岛素抵抗途径的贡献。