Regulation and Function of SUMO-1 Protein Modification

SUMO-1 蛋白修饰的调控和功能

• 批准号: 8062276
• 负责人: MICHAEL J. MATUNIS
• 金额: $ 33.08万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-03-01 至 2014-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8062276
• 关键词: Address; Affect; Amino Acids; Anaphase; Applications Grants; Binding; Binding Proteins; Biochemical; CENP-E protein; Cell Cycle; Cell Proliferation; Cell division; Cell physiology; Cells; Chromatin; Chromosome Structures; Chromosomes; Detection; Development; Enzymes; Funding; Goals; Human; Kinetochores; Knowledge; Lead; Malignant Neoplasms; Mammalian Cell; Mammals; Mediating; Mitosis; Mitotic; Modification; Molecular; Normal Cell; Phosphorylation; Play; Post-Translational Protein Processing; Process; Property; Proteins; Regulation; Research; Research Design; Role; Signal Transduction; Small Ubiquitin-Related Modifier Proteins; Structure; Testing; Ubiquitin; Ubiquitination; cancer therapy; isopeptidase; paralogous gene; public health relevance; segregation; telophase

DESCRIPTION (provided by applicant): SUMOs (small ubiquitin-related modifiers) are ~100 amino acid proteins that are posttranslationally and covalently conjugated to hundreds of other proteins and thereby regulate a wide range of cellular processes. We have found that sumoylation, like ubiquitination and phosphorylation, is an essential regulator of mitosis in mammalian cells. Mammals express three SUMO paralogs: SUMO-1, SUMO-2 and SUMO-3 (because SUMO-2 and SUMO-3 are 96% identical, they are referred to as SUMO-2/3). Our findings indicate that SUMO-1 and SUMO-2/3 are conjugated to unique subsets of proteins during mitosis and that they regulate distinct processes. However, many unanswered questions still exist. Many of the relevant targets of SUMO-1 and SUMO-2/3 modification remain to be identified and characterized, and mechanisms regulating their temporal modification in mitosis are not known. In addition, the specific molecular effects of SUMO-1 and SUMO-2/3 modification on their targets, and how these effects facilitate progression through mitosis, are still poorly understood. The goals of the research proposed in this renewal grant application are to address these questions and develop a detailed molecular understanding of how sumoylation affects progression through mitosis. These goals will be achieved through four specific aims: (1) We will define the roles that SUMO-2/3 modification and binding play in the targeting and assembly of kinetochore-associated proteins during mitosis. (2) We will identify and characterize molecular mechanisms regulating the temporal and spatial sumoylation of proteins during mitosis. (3) We will identify and characterize chromosome-associated proteins sumoylated during anaphase and telophase. (4) We will investigate the biophysical properties and functions of polymeric SUMO-2/3 chains and mitosis-related chain-binding proteins. PUBLIC HEALTH RELEVANCE: Understanding the factors and signals that regulate normal cell division is essential for a full understanding of the causes of human cancer and for development of new anti-cancer therapies. We have identified sumoylation (the covalent linkage of the SUMO protein to other cellular proteins) as a critical process required for normal cell division. Our studies are designed to provide a more complete understanding of how sumoylation regulates cell division at the molecular level. Knowledge gained from these studies has the potential to lead to the development of new strategies for both the detection and for the treatment of human cancers.

描述（由申请人提供）：sumo（小泛素相关修饰剂）是约100个氨基酸的蛋白质，它们在翻译后与数百种其他蛋白质共价偶联，从而调节广泛的细胞过程。我们发现summoylation，就像泛素化和磷酸化一样，是哺乳动物细胞有丝分裂的重要调节因子。哺乳动物表达三种相扑类比：SUMO-1、SUMO-2和SUMO-3（因为SUMO-2和SUMO-3 96%相同，所以它们被称为SUMO-2/3）。我们的研究结果表明，SUMO-1和SUMO-2/3在有丝分裂过程中与独特的蛋白质亚群结合，并调节不同的过程。然而，仍然存在许多未解之谜。SUMO-1和SUMO-2/3修饰的许多相关靶点仍有待鉴定和表征，有丝分裂中调节其时间修饰的机制尚不清楚。此外，SUMO-1和SUMO-2/3修饰对其靶标的特定分子作用，以及这些作用如何促进有丝分裂的进展，仍然知之甚少。这项研究的目标是解决这些问题，并对summoylation如何通过有丝分裂影响进展进行详细的分子理解。这些目标将通过以下四个具体目标来实现：(1)我们将定义SUMO-2/3修饰和结合在有丝分裂过程中着丝酶相关蛋白的靶向和组装中所起的作用。(2)我们将确定和表征有丝分裂过程中调节蛋白质时空聚合的分子机制。(3)我们将鉴定和表征染色体相关蛋白在后期和末期的聚合。(4)我们将研究聚合SUMO-2/3链和有丝分裂相关链结合蛋白的生物物理特性和功能。