Oxidative stress, telomere damage and Werner syndrome.

氧化应激、端粒损伤和维尔纳综合征。

• 批准号: 7586091
• 负责人: ROBERT Anthony MARCINIAK
• 金额: $ 29.33万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-15 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7586091
• 关键词: Age; Aging; Aging-Related Process; Antioxidants; Biological Assay; Breeding; Cell Aging; Cell Cycle; Cell Cycle Stage; Cell Line; Cell division; Cells; Chromosomes; Chronic; DNA; Data; Defect; Dependence; Deterioration; Development; Disease; Event; Exhibits; Exonuclease; Fibroblasts; Frequencies; Functional disorder; G-Quartets; Generations; Genes; Genetic Recombination; Growth; Hereditary Disease; Homologous Gene; Human; Human Cell Line; Human Genetics; In Vitro; Individual; Lesion; Link; Location; Longevity; Mediating; Modeling; Molecular Analysis; Mus; Mutant Strains Mice; Mutation; Nature; Organism; Oxidative Stress; Oxygen measurement, partial pressure, arterial; Pathology; Pathway interactions; Phenotype; Physiological; Population; Premature aging syndrome; Process; Proteins; Publishing; Recruitment Activity; Relative (related person); Research Personnel; Rest; Role; Signal Transduction; Sister; Sister Chromatid Exchange; Structure; Sum; Syndrome; System; Telomerase; Telomerase RNA Component; Telomere Maintenance; Testing; Time; Werner Syndrome; Yeasts; base; demographics; genetic analysis; helicase; human SOD2 protein; human WRN protein; immortalized cell; in vivo; insight; mutant; normal aging; novel; null mutation; oxidative damage; polypeptide; programs; repaired; research study; response; senescence; telomerase reverse transcriptase; telomere; tissue culture

DESCRIPTION (provided by applicant): As population demographics in the US continue to skew towards older ages, determining the processes that underlie the physical deterioration that occurs in normal aging becomes of increasing importance. An analysis of the genetics of human aging is possible and promises to yield new insight into these processes. The genes responsible for most genetic disorders of human premature aging have been identified. Werner's syndrome (WS) is one such disorder. The overall aim of this proposal is to use the molecular analysis of WS to better understand the aging process in the normal human population. WS is a human genetic disorder with features suggestive of accelerated aging. The gene defective in most cases of WS encodes a polypeptide with both helicase and exonuclease activities. Multiple studies support a role or roles of the WS protein in telomere maintenance. Telomere loss is predicted to reflect the sum of DNA lost uniformly at all telomeres during replication, and sporadic loss events occurring at individual telomeres with variable frequency. The latter class of events includes loss of telomere sequences due to damage to telomere DNA. Using a simple inhibition of colony formation assay, we have found that primary WS fibroblasts are defective in repair of oxidative telomere damage. Based on our preliminary data and published analyses of the effect of oxidative stress on telomere sequence loss in normal fibroblasts and studies of the role of WS protein in telomere processing, we suggest a model in which the WS protein participates in repair of damage to telomeres. In Aim 1, we will study the nature of the lesions produced by oxidative damage at telomeres and the mechanisms by which the cell recognizes and responds to this damage. In Aim 2, we will study the role of the WS protein in the response to telomere damage caused by oxidative stress. The mechanism by which telomerase suppresses the sensitivity of WS fibroblasts to oxidative stress will be determined in Aim 3. The studies in Aims 1-3 will be performed in tissue culture; to determine the in vivo relevance of the role of oxidative stress in the development of phenotypes related to telomere deficiency, in Aim 4 we will study mice that are deficient in combinations of the WS helicase, telomerase RNA component, and superoxide dismutase 2. These studies provide a novel link between oxidative stress, telomere dysfunction and a human progeroid syndrome. The relative contribution of sporadic loss events and end-replication inefficiency to rates of overall telomere sequence loss is currently unknown. Increased understanding of sporadic loss events and the pathways influencing their occurrence is of critical importance in devising strategies to minimize telomere loss.

描述(申请人提供)：随着美国人口结构继续向高龄倾斜，确定在正常老龄化过程中发生的身体退化的过程变得越来越重要。对人类衰老的遗传学进行分析是可能的，并有望对这些过程产生新的见解。导致人类早衰的大多数遗传性疾病的基因已经被确定。沃纳综合征(WS)就是这样一种障碍。这项建议的总体目标是使用WS的分子分析来更好地了解正常人群中的衰老过程。WS是一种人类遗传性疾病，具有加速衰老的特征。在大多数WS病例中，缺陷基因编码一种同时具有解旋酶和核酸外切酶活性的多肽。多项研究支持WS蛋白在端粒维持中的作用。端粒丢失被预测为反映复制过程中所有端粒均匀丢失的DNA的总和，以及个别端粒以不同频率发生的零星丢失事件。后一类事件包括端粒DNA损伤导致的端粒序列丢失。使用简单的克隆形成抑制实验，我们发现原代WS成纤维细胞在修复氧化端粒损伤方面存在缺陷。根据我们的初步数据和已发表的关于氧化应激对正常成纤维细胞端粒序列丢失的影响以及WS蛋白在端粒加工中作用的研究，我们提出了WS蛋白参与端粒损伤修复的模型。在目标1中，我们将研究端粒氧化损伤造成的损伤的性质，以及细胞识别和响应这种损伤的机制。在目标2中，我们将研究WS蛋白在氧化应激引起的端粒损伤反应中的作用。目标3将确定端粒酶抑制WS成纤维细胞对氧化应激敏感性的机制。在目标1-3中的研究将在组织培养中进行；为了确定氧化应激在与端粒缺乏相关的表型发展中的作用在体内的相关性，在目标4中，我们将研究WS解旋酶、端粒酶RNA成分和超氧化物歧化酶2的组合缺陷的小鼠。这些研究提供了氧化应激、端粒功能障碍和人类孕激素综合征之间的新联系。目前尚不清楚零星丢失事件和末端复制低效对整个端粒序列丢失率的相对贡献。增加对零星丢失事件和影响其发生的途径的了解，对于制定减少端粒丢失的策略至关重要。