Cell Cycle Regulation of IRP2 Phosphorylation During Hematopoiesis

造血过程中 IRP2 磷酸化的细胞周期调控

基本信息

批准号：
10639952
负责人：
Elizabeth Ann Leibold
金额：
$ 55.5万
依托单位：
UNIVERSITY OF UTAH
依托单位国家：
美国
项目类别：
财政年份：
2023
资助国家：
美国
起止时间：
2023-07-01 至 2027-06-30
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10639952
关键词：
3&apos Untranslated Regions Affect Alanine Alleles Anemia Binding Binding Proteins Blood Cell Count Bone Marrow Bone Marrow Cells Bone Marrow Transplantation CRISPR/Cas technology Cell Cycle Cell Cycle Arrest Cell Cycle Regulation Cell Death Cell Differentiation process Cell Lineage Cell Survival Cells Characteristics Codon Nucleotides DNA biosynthesis Development Duodenum Dysmyelopoietic Syndromes Elements Embryo Engineering Enterobacteria phage P1 Cre recombinase Enterocytes Erythroblasts Erythrocytes Erythroid Erythroid Cells Erythropoiesis Exhibits Ferritin Fibroblasts Flow Cytometry Functional disorder G2 Phase Gene Expression Generations Goals Hela Cells Hematological Disease Hematology Hematopoiesis Hematopoietic stem cells Heme Hemoglobin In Vitro Inherited Iron Iron Regulatory Protein 2 Knock-in Mouse LoxP-flanked allele Macrocytic Anemia Mediating Messenger RNA Mitochondria Mitosis Molecular Mouse Strains Mus Mutate Oxidative Stress Oxygen Pathway interactions Persons Phenotype Phosphorylation Physiological Population Process Production Proliferating Proteins Proteomics RNA RNA Binding Reporting Respiration Role S phase SKP Cullin F-Box Protein Ligases Serine Serum Spleen Splenomegaly Supporting Cell System TFRC gene Testing Tissues Translations Transplantation cell growth cell growth regulation cofactor erythroid differentiation in vivo insight iron deficiency iron metabolism mRNA Stability mRNA Translation metal transporting protein 1 mouse model mutant novel posttranscriptional single-cell RNA sequencing stem stem cell proliferation transplant model ubiquitin ligase uptake

项目摘要

ABSTRACT Iron is essential for cellular growth due to its role as a cofactor in proteins involved in DNA synthesis, mitochondrial respiration and hemoglobin production. Vertebrate iron metabolism is controlled post- transcriptionally by iron-regulatory protein 2 (Irp2). Irp2 binds to iron-responsive elements (IREs) in the mRNAs of proteins involved in iron uptake (transferrin receptor 1), sequestration (ferritin) and export (ferroportin), and regulates the translation or stability of these mRNAs. During iron deficiency, Irp2 binds IREs to regulate mRNA translation or stability, whereas during iron sufficiency, Irp2 is degraded by the FBXL5-SCF ubiquitin ligase. Here we show that Irp2 is regulated by iron-independent phosphorylation of Ser157 during G2/M that disrupts its interaction with ferritin IRE mRNA during mitosis and depresses ferritin translation. Expression of Irp2-S157A in Irp2KO-MEFs causes a G2/M delay and slows proliferation. The significance of S157 phosphorylation was investigated in mice where Ser157 was mutated to Ala157 (Irp2A/A)). Irp2A/A mice exhibit macrocytic anemia, defective erythroid terminal differentiation, splenomegaly, and dysregulated systemic iron metabolism. We propose that cell-cycle regulation of ferritin and other IRE-mRNAs may provide a mechanism to modulate the cellular labile iron pool during the cell cycle. Our overall goal is to determine how loss of S157 phosphorylation perturbs erythropoiesis and causes anemia. Our aims are to 1) determine the cell-autonomous role for Irp2- S157 phosphorylation in erythropoiesis by bone marrow (BM) transplantation and flow cytometric analysis of cell-cycle status, proliferation, iron and other parameters, 2) identify mechanisms underlying dysregulated erythropoiesis in Irp2A/A mice using a mouse erythroblast in vitro differentiation system with WT and Irp2A/A BM cells, and proteomic analysis of erythroblast populations to identify protein changes between WT and Irp2A/A cells, and 3) generate an erythroid-specific Irp2A/A knockin mouse model to study erythroid terminal differentiation. We anticipate that our studies will provide new insights of normal and dysregulated erythropoiesis.

抽象的铁对于细胞生长至关重要，因为它是参与 DNA 合成的蛋白质的辅助因子，线粒体呼吸和血红蛋白产生。脊椎动物的铁代谢在后期受到控制由铁调节蛋白 2 (Irp2) 转录。 Irp2 与 mRNA 中的铁反应元件 (IRE) 结合参与铁摄取（转铁蛋白受体 1）、隔离（铁蛋白）和输出（铁转运蛋白）的蛋白质，以及调节这些 mRNA 的翻译或稳定性。缺铁期间，Irp2 结合 IRE 来调节 mRNA 翻译或稳定性，而在铁充足期间，Irp2 被 FBXL5-SCF 泛素连接酶降解。在这里，我们表明 Irp2 在 G2/M 期间受到与铁无关的 Ser157 磷酸化的调节，从而破坏它在有丝分裂过程中与铁蛋白 IRE mRNA 相互作用并抑制铁蛋白翻译。 Irp2-S157A的表达 Irp2KO-MEF 中的 Irp2KO-MEF 会导致 G2/M 延迟并减慢增殖。 S157磷酸化的意义是在 Ser157 突变为 Ala157 (Irp2A/A) 的小鼠中进行了研究。 Irp2A/A小鼠表现出大细胞性贫血，红系终末分化缺陷、脾肿大和全身铁代谢失调。我们提出铁蛋白和其他 IRE-mRNA 的细胞周期调节可能提供一种调节机制细胞周期期间细胞不稳定的铁库。我们的总体目标是确定 S157 磷酸化的丧失是如何发生的干扰红细胞生成并导致贫血。我们的目标是 1) 确定 Irp2 的细胞自主作用- 骨髓 (BM) 移植红细胞生成中的 S157 磷酸化和流式细胞术分析细胞周期状态、增殖、铁和其他参数，2) 确定失调的机制使用具有 WT 和 Irp2A/A BM 的小鼠成红细胞体外分化系统在 Irp2A/A 小鼠中进行红细胞生成细胞和成红细胞群体的蛋白质组学分析，以确定 WT 和 Irp2A/A 之间的蛋白质变化细胞，3) 生成红细胞特异性 Irp2A/A 敲入小鼠模型来研究红细胞末端差异化。我们预计我们的研究将为正常和失调提供新的见解红细胞生成。