Defining the human telomere signaling networks and their implication in cancer

定义人类端粒信号网络及其在癌症中的意义

• 批准号: 8306885
• 负责人: Zhou Songyang
• 金额: $ 29.58万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-01 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8306885
• 关键词: Binding; Biology; Cell Survival; Cells; Chromatin; Chromosome abnormality; Collection; Complex; DNA Damage; DNA Replication Damage; Development; Disease; Early Diagnosis; Enzymes; Fluorescence; Functional disorder; Gene Expression; Genetic Recombination; Genetic Transcription; Genome; Genome Stability; Genomic Instability; Goals; Growth and Development function; Homeostasis; Human; Length; Light; Link; Malignant Neoplasms; Mammalian Cell; Maps; Mediating; Methodology; Methods; Molecular; Mutation; Normal Cell; Pathway interactions; Phosphoric Monoester Hydrolases; Phosphorylation; Post-Translational Protein Processing; Premature aging syndrome; Protein Binding; Protein phosphatase; Proteins; Proteomics; Recruitment Activity; Regulation; Resolution; Role; SHPS-1 protein; Scanning; Screening procedure; Sequence Analysis; Signal Pathway; Signal Transduction; Site; TERF1 gene; TINF2 gene; Telomerase; Telomere Maintenance; Telomere-Binding Proteins; Telomeric Repeat Binding Protein 1; Therapeutic; Transcriptional Regulation; Ubiquitination; Work; age related; base; cellular targeting; design; effective therapy; genome-wide; human disease; insight; interstitial; loss of function; novel; protein function; protein protein interaction; response; telomere; therapy development; tumorigenesis; ubiquitin-protein ligase

DESCRIPTION (provided by applicant): Telomere dysfunction is a well-documented contributing factor to diseases such as cancer. Our proposed work should identify new targets and pathways and provide mechanistic details of their function, thereby facilitating in our identifying novel targets for therapies, gaining new insight into the pathways and signals for disease initiation, and shedding light on new and more effective treatment options. We hypothesize that distinct and uncharacterized classes of signaling and regulatory proteins bind directly to core telomeric proteins and modulate telomere homeostasis. Our long-term goal is to elucidate the mechanisms by which telomeric proteins and their associated factors regulate various signaling pathways at the telomeres. The goal of this project is to systematically identify novel regulators recruited to the telomeres by telomeric proteins such as TRF2, and to study how these targets may participate in telomere regulation. The specific aims of the proposal are: Specific Aim 1: To systematically identify new telomere regulators and signaling networks. Genome-wide approaches will be employed to identify new cellular targets of TRF2, and generate high-resolution maps of TRF2-centric signaling networks. Secondary screens are proposed to confirm and prioritize the targets identified. Specific Aim 2: To determine the function of the newly identified regulators. This aim will focus on new TRF2 targets PNUTS and ubiquitin E3 ligases, in their regulation of TRF2 function and telomere maintenance, and possible roles in extra-telomeric activities.

描述（由申请人提供）：端粒功能障碍是一个有充分证据的疾病因素，如癌症。我们提出的工作应该确定新的靶点和途径，并提供其功能的机制细节，从而促进我们确定新的治疗靶点，获得疾病起始的途径和信号的新见解，并揭示新的和更有效的治疗方案。我们假设，不同的和未表征的信号和调节蛋白直接结合到核心端粒蛋白和调节端粒稳态。我们的长期目标是阐明端粒蛋白及其相关因子调控端粒各种信号通路的机制。该项目的目标是系统地识别端粒蛋白（如TRF2）募集到端粒的新型调节因子，并研究这些靶点如何参与端粒调节。该提案的具体目标是：具体目标1：系统地识别新的端粒调节器和信号网络。全基因组方法将用于鉴定TRF2的新细胞靶点，并生成以TRF2为中心的信号网络的高分辨率地图。建议进行二次筛选，以确认确定的目标并对其进行优先排序。具体目标2：确定新确定的监管机构的功能。本研究将重点关注新的TRF2靶点PNUTS和泛素E3连接酶对TRF2功能和端粒维持的调节，以及它们在端粒外活性中的可能作用。