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Chromatin Degradation and Cell Clearance During Apoptosis

细胞凋亡过程中染色质降解和细胞清除

基本信息

批准号：
7354072
负责人：
DING XUE
金额：
$ 26.57万
依托单位：
UNIVERSITY OF COLORADO
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-03-01 至 2011-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7354072
关键词：
Affect Animals Apoptosis Apoptotic Autoimmune Diseases Biochemical Biochemical Genetics Biological Biological Assay Caenorhabditis elegans Cancer Etiology Cell Count Cell Death Cell Proliferation Cells Chromatin Chromosomes Cloning Complex DNA Defect Degradation Pathway Development Eating Endopeptidases Equilibrium Event Excision Failure Genes Genetic Genetic Screening Genome Goals Homeostasis Immune Immune response In Situ Nick-End Labeling In Vitro Inflammation Knowledge Lead Malignant Neoplasms Mediating Methods Molecular Molecular Genetics Neurodegenerative Disorders Pathway interactions Pattern Peptide Hydrolases Phenotype Physiological Play Process Property Proteins RNA Interference Regulation Research Personnel Role Signal Transduction Site Surface Tissues Work base cell killing genetic analysis human disease in vivo insight mutant novel novel therapeutics nuclease preference prevent programs research study therapeutic target uncontrolled cell growth

项目摘要

DESCRIPTION (provided by applicant): As a normal aspect of animal development and tissue homeostasis, apoptosis plays an essential role in maintaining the physiological balance of appropriate cell numbers by opposing uncontrolled cell proliferation. Abnormal inactivation or activation of apoptosis can lead to uncontrolled cell growth or uncontrolled cell death and may result in human diseases such as cancer, neurodegenerative diseases, and autoimmune disorders. The broad and long-term objectives of this application are to understand the basic mechanisms underlying the control and execution of apoptosis and to use knowledge from such studies to develop new methods to treat and prevent apoptosis-related human diseases, especially caner. Chromosome fragmentation is a hallmark of apoptosis and a critical step in cell death execution. During apoptosis, a battery of nucleases are activated and act cooperatively and sequentially to promote fragmentation of chromosomal DNA. Seven new cell death-related nucleases (CRN nucleases) have been identified in C. elegans and found to act in at least two distinct pathways and two different functioning sites to promote DNA degradation and clearance of apoptotic cells during apoptosis. The goal of this application is to carry out biochemical, molecglar genetic, and cell biological studies in C. elegans to dissect the apoptotic DNA degradation machinery and to unravel the basic molecular mechanisms that regulate the execution of apoptotic DNA degradation and clearance of apoptotic cells. The specific aims are: 1) to carry out biochemical, molecular genetic, and functional analyses of C. elegans crn genes to understand how they work together to promote apoptotic DNA degradation; 2) to identify and characterize additional genes that are important for apoptotic DNA degradation; 3) to investigate how the chromosome fragmentation process affects clearance of apoptotic cells, another critical cell death execution event involved in tissue remodeling, suppression of inflammation, and regulation of immune reponses. The studies of the molecular components and biochemical mechanisms that regulate chromatin degradation and cell clearance during apoptosis will provide crucial insights into how cell death is executed and should contribute to the understanding of the basic mechanisms that regulate apoptosis in general.

描述（由申请人提供）：作为动物发育和组织稳态的正常方面，细胞凋亡通过对抗不受控制的细胞增殖，在维持适当细胞数量的生理平衡中发挥重要作用。细胞凋亡的异常失活或激活可导致不受控制的细胞生长或不受控制的细胞死亡，并可能导致人类疾病，例如癌症、神经退行性疾病和自身免疫性疾病。该应用的广泛和长期目标是了解细胞凋亡控制和执行的基本机制，并利用此类研究的知识开发新方法来治疗和预防与细胞凋亡相关的人类疾病，特别是癌症。染色体断裂是细胞凋亡的标志，也是细胞死亡执行的关键步骤。在细胞凋亡过程中，一系列核酸酶被激活并依次协同作用，促进染色体 DNA 断裂。在秀丽隐杆线虫中鉴定出七种新的细胞死亡相关核酸酶（CRN 核酸酶），并发现其在至少两个不同的途径和两个不同的功能位点中发挥作用，以促进凋亡细胞在凋亡过程中的 DNA 降解和清除。本申请的目标是在秀丽隐杆线虫中进行生化、分子遗传学和细胞生物学研究，以剖析凋亡 DNA 降解机制，并揭示调节凋亡 DNA 降解和凋亡细胞清除执行的基本分子机制。具体目标是：1）对线虫crn基因进行生化、分子遗传学和功能分析，了解它们如何协同作用促进凋亡DNA降解； 2) 鉴定和表征对细胞凋亡 DNA 降解很重要的其他基因； 3) 研究染色体断裂过程如何影响凋亡细胞的清除，这是参与组织重塑、抑制炎症和调节免疫反应的另一个关键细胞死亡执行事件。对细胞凋亡过程中调节染色质降解和细胞清除的分子成分和生化机制的研究将为细胞死亡如何执行提供重要的见解，并有助于理解一般调节细胞凋亡的基本机制。