Proteolytic Control of Iron Metabolism by the Ubiquitin Ligase FBXL5

泛素连接酶 FBXL5 对铁代谢的蛋白水解控制

• 批准号: 8499363
• 负责人: James Akira Wohlschlegel
• 金额: $ 28.56万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8499363
• 关键词: Binding; Biochemical; Biochemical Pathway; Biogenesis; Biological; Cell Respiration; Cells; Communication; Coupled; DNA Repair; Dependence; Development; Diabetes Mellitus; Disease; Energy Metabolism; Equilibrium; Gene Expression; Goals; Hemerythrin; Homeostasis; Homologous Gene; Human; Huntington Disease; Investigation; Iron; Iron Regulatory Protein 2; Iron-Sulfur Proteins; Knowledge; Laboratories; Life; Malignant Neoplasms; Mediating; Molecular; Neurodegenerative Disorders; Nuclear; Nutrient; Oxidative Stress; Pathway interactions; Play; Post-Translational Protein Processing; Post-Translational Regulation; Process; Protein S; Proteins; Proteomics; Regulation; Role; Saccharomycetales; Set protein; Signal Transduction; Sulfur; System; Testing; Toxic effect; Transcriptional Regulation; Ubiquitin; Ubiquitination; Work; base; insight; iron metabolism; mRNA Stability; malignant breast neoplasm; meetings; multicatalytic endopeptidase complex; novel; novel therapeutics; nucleotide metabolism; overexpression; prevent; public health relevance; research study; response; tumorigenesis; ubiquitin ligase; ubiquitin-protein ligase; uptake; yeast protein

DESCRIPTION (provided by applicant): Iron is an essential nutrient that functions as a key co-factor for many cellular proteins involved in aerobic respiration, nucleotide metabolism, gene expression, and DNA repair. Given its central role in sustaining life, it is not surprising that cells have established a variety of elaborate regulatory mechanisms to control iron availability and usage. While characterizing components of the ubiquitination machinery that are deregulated in tumorigenesis, we identified a ubiquitin ligase subunit called FBXL5. In preliminary work, we demonstrated the FBXL5 is a novel regulator of iron metabolism that proteolytically controls the expression of important effectors of iron metabolism and cytoplasmic iron-sulfur cluster assembly. The major goal of this proposal is to examine the biological mechanisms by which FBXL5 regulates and is regulated by iron-related pathways. In specific aim 1, we will examine the molecular basis of the iron-regulated interaction of FBXL5 with IRP2, a key regulator of iron homeostasis. The experiments in specific aim 2 will revolve around the regulation of FBXL5 itself and elucidating the novel proteolytic pathway responsible for its proteasome-dependent degradation under conditions of low iron availability. Specific aim 3 will focus on the establishing the functional relevance of the interaction between FBXL5 and MMS19 and CIAO1, two putative components of the cytosolic iron assembly (CIA) pathway which is required for the assembly of Fe/S clusters in extramitochondrial proteins. Investigation of these three aims will provide a comprehensive view of how FBXL5 is able to influence multiple iron-associated processes. Ultimately, we hope that this work will offer insight into how the deregulation of FBXL5 and its downstream pathways may contribute to tumorigenesis while simultaneously highlighting potential new therapeutic strategies.

描述（由申请人提供）：铁是一种必需营养素，作为参与有氧呼吸、核苷酸代谢、基因表达和DNA修复的许多细胞蛋白质的关键辅因子发挥作用。鉴于其在维持生命中的核心作用，细胞建立了各种复杂的调节机制来控制铁的可用性和使用也就不足为奇了。在表征肿瘤发生中失调的泛素化机制的组成部分时，我们鉴定了一种称为FBXL 5的泛素连接酶亚基。在前期工作中，我们证明了FBXL 5是一种新的铁代谢调节剂，其通过蛋白水解控制铁代谢和细胞质铁硫簇组装的重要效应子的表达。该提案的主要目标是研究FBXL 5调节的生物学机制以及铁相关途径的调节。在具体目标1中，我们将研究FBXL 5与IRP 2（铁稳态的关键调节因子）的铁调节相互作用的分子基础。具体目标2中的实验将围绕FBXL 5本身的调节，并阐明在低铁可用性条件下负责其蛋白酶体依赖性降解的新型蛋白水解途径。具体目标3将集中于建立FBXL 5和MMS 19和CIA 01之间相互作用的功能相关性，这是线粒体外蛋白质中Fe/S簇组装所需的细胞溶质铁组装（CIA）途径的两个推定组分。这三个目标的调查将提供一个全面的看法FBXL 5是如何能够影响多个铁相关的过程。最终，我们希望这项工作能够深入了解FBXL 5及其下游通路的失调如何有助于肿瘤发生，同时突出潜在的新治疗策略。