Genetic Studies of Diabetes

糖尿病的遗传学研究

• 批准号: 9770835
• 负责人: CARL S. THUMMEL
• 金额: $ 38.13万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-09-30 至 2021-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9770835
• 关键词: Adult; Affect; Animal Model; Animals; Beta Cell; Binding; Biological Models; Biology; Cells; Cellular biology; ChIP-seq; Clinic; Defect; Development; Diabetes Mellitus; Disease; Drosophila genus; Evolution; Fat Body; Foundations; Future; Gene Expression; Gene Expression Profiling; Genes; Genetic; Genetic study; Glucose; Glucose Intolerance; Goals; HNF4A gene; Health; Heart Diseases; Homeostasis; Human; Hyperglycemia; Impairment; Incidence; Inflammation; Inflammatory Response Pathway; Inherited; Insulin; Insulin-Dependent Diabetes Mellitus; Intestines; Kidney Failure; Link; Liver; Mammals; Messenger RNA; Metabolic; Metabolic dysfunction; Metabolic syndrome; Metabolism; Mitochondria; Mitochondrial Proteins; Molecular; Mutation; Neurobiology; Non-Insulin-Dependent Diabetes Mellitus; Nuclear; Nuclear Receptors; Orthologous Gene; Pancreas; Pathway interactions; Patients; Pattern; Peripheral; Phenotype; Physiological; Physiology; Protein Isoforms; Proteins; RNA Interference; Research; Research Design; Risk Factors; Role; Signal Transduction; Stroke; Structure of beta Cell of islet; System; Testing; Therapeutic; Tissues; Work; associated symptom; blood glucose regulation; combat; defined contribution; design; experimental study; fly; functional group; gene function; genome-wide; improved; insight; insulin secretion; insulin signaling; liver metabolism; mitochondrial dysfunction; mitochondrial genome; mouse model; mutant; novel strategies; novel therapeutic intervention; prevent; receptor; transcription factor; transcriptome sequencing

In addition to the widely studied type 1 and type 2 diabetes, there are a number of monogenic inherited forms of this disorder, including Maturity-Onset Diabetes of the Young (MODY). The genetic basis for the first MODY subtype was discovered 20 years ago through its association with mutations in the HNF4A nuclear receptor. This link with a transcription factor focused efforts on defining the central roles of Hnf4A in the key tissues where it controls metabolism: the liver, intestine, and pancreas. Genetic studies in mouse models, however, did not recapitulate the full range of symptoms associated with MODY1 – in particular, the sustained hypoinsulinemic hyperglycemia seen in the clinic. We discovered that the expression pattern of HNF4A is conserved through evolution, from flies to mammals, and that mutants for the Drosophila ortholog of Hnf4A (dHNF4) display a range of phenotypes that resemble those of MODY1 patients. These include adult-onset hyperglycemia, impaired glucose-stimulated insulin secretion, glucose intolerance, and reduced peripheral insulin signaling. In addition, our RNA-seq transcriptional profiling identified several functional groups of dHNF4-regulated genes that act in the tissues where the receptor is expressed in flies and humans. This includes widespread effects on inflammatory response pathways, similar to the role of Hnf4A in the mammalian intestine, as well as key genes involved in glucose-stimulated insulin secretion. Unexpectedly, we also discovered that mitochondrial-encoded gene expression is significantly reduced in the mutant, and that dHNF4 protein localizes to mitochondria and binds specifically to the control region of the mitochondrial genome. dHNF4 also directly regulates nuclear genes that encode mitochondrial proteins, demonstrating a central role in mitochondrial physiology. Given that only a few nuclear transcription factors have been identified in mitochondria, and their roles are poorly understood, we propose to undertake a detailed analysis of the mitochondrial functions of dHNF4 and link these to key downstream roles of the receptor. In addition, we will use Drosophila genetics to elucidate the interactions between mitochondrial dysfunction, inflammation, and metabolic defects in the context of diabetes. Although these pathways are often associated in metabolic syndrome, their cause and effect relationships remain unclear. Our overall hypothesis is that dHNF4 acts in multiple tissues to maintain mitochondrial function and to suppress inflammation and diabetes. We propose three specific aims to (1) determine the tissue-specific functions of dHNF4, (2) determine the physiological functions of dHNF4-regulated pathways and target genes, and (3) characterize the evolutionary conservation of dHNF4 functions, from flies to mammals. Taken together, this research will provide a simple genetic system to dissect the interplay between mitochondrial dysfunction, inflammation, and diabetes, as well as an animal model for MODY1. Our results, in turn, can be used to guide future studies in mouse models as well as devise new potential therapeutic approaches for preventing and treating diabetes in humans.

除了被广泛研究的1型和2型糖尿病外，还有许多单基因遗传形式 这种疾病，包括成熟型青年糖尿病(MODY)。第一个MODY的遗传学基础 亚型是20年前通过与HNF4a核受体突变有关而被发现的。 这种与转录因子的联系集中在确定HNF4a在关键组织中的中心作用上 它控制新陈代谢的地方：肝脏、肠道和胰腺。然而，在小鼠模型中进行的遗传学研究， 没有概括与MODY1相关的所有症状-特别是持续的 临床上可见低血糖性高血糖。我们发现HNF4a的表达模式是 在进化中保守，从苍蝇到哺乳动物，以及HNF4a的果蝇直系突变体 (DHNF4)表现出一系列与MODY1患者相似的表型。其中包括成人发病 高血糖、葡萄糖刺激的胰岛素分泌受损、糖耐量异常和外周血细胞减少 胰岛素信号。此外，我们的rna-seq转录图谱鉴定了几个功能基团。 DHNF4调节的基因，作用于苍蝇和人类中表达受体的组织。这 包括对炎症反应途径的广泛影响，类似于HNF4a在哺乳动物中的作用 肠道，以及参与葡萄糖刺激的胰岛素分泌的关键基因。没想到，我们也 发现线粒体编码的基因在突变体中的表达显著降低，dHNF4 蛋白质定位于线粒体，并与线粒体基因组的控制区特异结合。 DHNF4还直接调节编码线粒体蛋白的核基因，显示出核心作用 在线粒体生理学方面。考虑到只有几个核转录因子在 线粒体，以及它们的作用鲜为人知，我们建议对 DHNF4的线粒体功能，并将这些与受体的关键下游作用联系起来。此外，我们还将 利用果蝇遗传学阐明线粒体功能障碍、炎症和 糖尿病背景下的代谢缺陷。尽管这些途径通常与代谢有关 它们之间的因果关系尚不清楚。我们的总体假设是dHNF4在 多种组织，维持线粒体功能，抑制炎症和糖尿病。我们建议 三个特定目的：(1)确定dHNF4的组织特异性功能；(2)确定生理功能 DHNF4调控途径和靶基因的功能，以及(3)进化保守的特征 DHNF4的功能，从苍蝇到哺乳动物。总而言之，这项研究将提供一个简单的遗传系统 解剖线粒体功能障碍、炎症和糖尿病之间的相互作用，以及一个动物 MODY1型号。反过来，我们的结果可以用来指导未来对小鼠模型的研究，以及设计 预防和治疗人类糖尿病的新的潜在治疗方法。