Post-Translational and Epigenetic Control of Branched-Chain Amino Acid Metabolism

支链氨基酸代谢的翻译后和表观遗传控制

• 批准号: 10225807
• 负责人: Matthew D Hirschey
• 金额: $ 12.26万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2018
• 资助国家: 美国
• 起止时间: 2018-06-01 至 2022-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10225807
• 关键词: Acetyl Coenzyme A; Acetylation; Acyl Coenzyme A; Acylation; Address; Adult; Affect; Biological; Branched-Chain Amino Acids; Carbon; Catabolism; Complex; Complications of Diabetes Mellitus; Coupling; Data; Defect; Development; Diabetes Mellitus; Diet; Disease; Enzymes; Epigenetic Process; Event; Excision; Experimental Designs; Family; Foundations; Functional disorder; Gene Expression; Genetic Transcription; Glucose; Goals; Health; Hepatic; Histone Acetylation; Histones; Homeostasis; Human; Insulin Resistance; Intervention; Isotope Labeling; Knowledge; Laboratories; Lead; Leucine; Lipids; Lysine; Macronutrients Nutrition; Maps; Measurement; Measures; Metabolic; Metabolic Control; Metabolic Pathway; Metabolism; Methods; Mission; Mitochondria; Mitochondrial Proteins; Modeling; Modification; Molecular; Mus; Names; Non-Insulin-Dependent Diabetes Mellitus; Nutrient; Obesity; Overnutrition; Pathway interactions; Peptides; Pharmacology; Physiological; Plasma; Play; Post-Translational Protein Processing; Prevention; Protein Acetylation; Proteins; Proteome; Proteomics; Public Health; Publishing; Reader; Reagent; Regulation; Research; Role; SIRT1 gene; Shapes; Sirtuins; Site-Directed Mutagenesis; Sum; Technology; Tissues; United States National Institutes of Health; acyl group; amino acid metabolism; deacylation; detection of nutrient; epigenome; genetic manipulation; histone modification; innovation; metabolomics; non-histone protein; novel; novel therapeutics; nutrient metabolism; oxidation; prevent; response; theories

Understanding the molecular mechanisms that contribute to dysregulated metabolism in diabetes is essential for developing effective prevention methods and discovering a cure. Over the past 10 years, substantial evidence supports the mitochondrial overload theory of overnutrition-induced metabolic dysregulation, including a specific role for dysregulated branched-chain amino acid (BCAA) metabolism. The goal here is to identify how acyl-CoA species derived from BCAA metabolism induce protein and histone modifications, and to assess how protein hyperacylation affects metabolic regulation in the setting of overnutrition. We recently discovered a class of highly reactive acyl-CoA species derived from leucine oxidation that modify enzymes involved in BCAA catabolism. We also uncovered a novel enzymatic activity of the mitochondrial sirtuin SIRT4 to remove these modifications, thereby regulating leucine catabolic flux. These discoveries define a new paradigm of protein acylation and deacylation, and identify an unexpected level of control over BCAA metabolism and nutrient homeostasis. In this project, we will build upon these findings and focus on the following Specific Aims: 1) To determine how alterations in nutrient flux lead to changes in mitochondrial protein acylation; 2) To determine the consequence of mitochondrial protein hyperacylation on BCAA enzyme function in the setting of over-nutrition; and 3) To determine how metabolites derived from nutrient metabolism are sensed and integrated into the epigenome. Together, these studies combine a comprehensive experimental design and an innovative conceptual framework in order to determine how intermediary metabolites derived from central carbon metabolism drive specific nutrient-sensing responses. Furthermore, this study will build a foundation of knowledge to further how these pathways contribute to the pathophysiology of diabetes. Ultimately, these studies will deepen our understanding of emergent, novel metabolic control mechanisms, and have the potential to inform the development of new therapies and prevention methods.

了解导致糖尿病代谢失调的分子机制对于开发有效的预防方法和发现治愈方法至关重要。在过去的10年中，大量的证据支持营养过剩诱导的代谢失调的线粒体过载理论，包括失调的支链氨基酸（BCAA）代谢的特定作用。本研究的目的是确定BCAA代谢产生的酰基辅酶A如何诱导蛋白质和组蛋白修饰，并评估蛋白质过度酰化如何影响营养过剩环境中的代谢调节。我们最近发现了一类高活性的酰基辅酶A物种，来自亮氨酸氧化，修饰参与BCAA催化剂的酶。我们还发现了线粒体sirtuin SIRT 4的一种新的酶活性，以去除这些修饰，从而调节亮氨酸分解代谢通量。这些发现定义了蛋白质酰化和去酰化的新范式，并确定了对BCAA代谢和营养稳态的意想不到的控制水平。在这个项目中，我们将建立在这些发现的基础上，并专注于以下具体目标：1）确定营养通量的改变如何导致线粒体蛋白酰化的变化; 2）确定在营养过剩的情况下，线粒体蛋白酰化对BCAA酶功能的影响; 3）确定营养代谢产生的代谢物如何被感知并整合到表观基因组中。总之，这些研究结合了联合收割机一个全面的实验设计和创新的概念框架，以确定如何中间代谢物来自中央碳代谢驱动特定的营养感应反应。此外，这项研究将建立一个知识基础，以进一步了解这些途径如何促进糖尿病的病理生理学。最终，这些研究将加深我们对新的代谢控制机制的理解，并有可能为新疗法和预防方法的开发提供信息。