Monitoring mechanisms in mammalian ribosome biogenesis

哺乳动物核糖体生物发生的监测机制

基本信息

批准号：
7340764
负责人：
DIMITRI G PESTOV
金额：
$ 23.07万
依托单位：
UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-02-01 至 2010-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7340764
关键词：
Address Anabolism Binding Biochemical Biochemical Genetics Biogenesis Cell Cycle Arrest Cell Cycle Checkpoint Cell Proliferation Cells Complex Defect Dissection Family member GTP-Binding Proteins Goals Guanine Nucleotides Guanosine Triphosphate Phosphohydrolases Hydrolysis In Vitro Link Malignant Neoplasms Mammalian Cell Mediating Mediator of activation protein Medical Surveillance Methods Modeling Molecular Monitor Mus Mutation Nucleolar Proteins Pathway interactions Play Process Property Protein p53 Proteins Refractory Ribosomal RNA Ribosomes Role Signal Transduction Stress System TP53 gene Therapeutic Intervention cell growth conformational conversion design human disease in vivo insight mutant novel research study response sensor

Address Anabolism Binding Biochemical Biochemical Genetics Biogenesis Cell Cycle Arrest Cell Cycle Checkpoint Cell Proliferation Cells Complex Defect Dissection Family member GTP-Binding Proteins Goals Guanine Nucleotides Guanosine Triphosphate Phosphohydrolases Hydrolysis In Vitro Link Malignant Neoplasms Mammalian Cell Mediating Mediator of activation protein Medical Surveillance Methods Modeling Molecular Monitor Mus Mutation Nucleolar Proteins Pathway interactions Play Process Property Protein p53 Proteins Refractory Ribosomal RNA Ribosomes Role Signal Transduction Stress System TP53 gene Therapeutic Intervention cell growth conformational conversion design human disease in vivo insight mutant novel research study response sensor

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项目摘要

DESCRIPTION (provided by applicant): Synthesis of new ribosomes is an essential cellular activity and it is becoming increasingly clear that ribosome biogenesis plays an important role in cancer and human disease. However, molecular mechanisms of this highly complex process and its links to other cellular pathways remain inadequately understood, especially in a mammalian system. Recent evidence indicates that mammalian cells possess a surveillance system that communicates perturbations in ribosome synthesis to the tumor suppressor p53. It is currently unknown how errors in ribosome assembly are recognized and which components in the ribosome biogenesis machinery mediate signaling to the p53 pathway. We seek to understand the mechanisms that provide monitoring of ribosome biogenesis in mammalian cells through analysis of the newly discovered nucleolar GTP-binding proteins (GTPases) Nog1 and Nug1A/B. Recent experimental evidence shows that the function of these GTPases is essential for synthesis of 60S ribosomal subunits and also implicates them as potential signaling links between ribosome synthesis and proliferation control pathways. The studies proposed here are designed to elucidate the role of the mammalian nucleolar GTPases in surveillance of ribosome biogenesis and to gain insight into the molecular mechanisms of their action. We will begin by addressing two questions to assess the monitoring function of the nucleolar GTPases. What is the role of mouse Nog1 and Nug1A/B in rRNA maturation? How does their function contribute to the accuracy of ribosome biogenesis and signaling to the p53 network? By using a combination of biochemical and genetic approaches, we will further investigate the molecular mechanisms of a model representative of the group, Nog1. What role do guanine nucleotide binding and hydrolysis play in the activities of this GTPase? What proteins serve as effectors and regulators of Nog1 function and how do they influence its GTPase cycle? Collectively, these studies should provide significant new information on a novel group of GTP-binding proteins, yield mechanistic insights into ribosome assembly and contribute to our understanding of the link between ribosome biogenesis and proliferation control in mammalian cells.

描述（由申请人提供）：新核糖体的合成是一种必不可少的细胞活性，越来越清楚核糖体生物发生在癌症和人类疾病中起重要作用。然而，这种高度复杂的过程的分子机制及其与其他细胞途径的联系仍然不足，尤其是在哺乳动物系统中。最近的证据表明，哺乳动物细胞具有监测系统，该系统将核糖体合成中的扰动传达到肿瘤抑制p53中。目前尚不清楚核糖体组装中的误差如何被识别，以及核糖体生物发生机械中哪些组件介导信号传导到p53途径。我们试图通过分析新发现的核仁GTP结合蛋白（GTPases）NOG1和NUG1A/B来了解哺乳动物细胞中核糖体生物发生的机制。最近的实验证据表明，这些GTPases的功能对于60S核糖体亚基的合成至关重要，并且也将它们视为核糖体合成与增殖控制途径之间的潜在信号连接。此处提出的研究旨在阐明哺乳动物核仁GTPases在核糖体生物发生监测中的作用，并深入了解其作用的分子机制。我们将首先解决两个问题，以评估核仁GTPase的监测功能。小鼠NOG1和NUG1A/B在rRNA成熟中的作用是什么？它们的功能如何有助于核糖体生物发生和对p53网络的信号传导的准确性？通过结合生化方法和遗传方法，我们将进一步研究代表该组NOG1的模型的分子机制。鸟嘌呤核苷酸结合和水解在该GTPase的活性中起什么作用？哪些蛋白质是NOG1功能的效应子和调节剂，它们如何影响其GTPase周期？总的来说，这些研究应提供有关一组新型GTP结合蛋白的重要新信息，对核糖体组装的机理见解，并有助于我们理解哺乳动物细胞中核糖体生物发生与增殖控制之间的联系。