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Defining the Functional Role of a Novel MS Susceptibility Gene, IL7R alpha chain

定义新型 MS 易感基因 IL7R α 链的功能作用

基本信息

批准号：
7920153
负责人：
SIMON G GREGORY
金额：
$ 34.94万
依托单位：
DUKE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-09-01 至 2014-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7920153
关键词：
6p21.3 Affect Alleles Alternative Splicing Architecture Autoimmunity Binding Biological CD8B1 gene Candidate Disease Gene Cell Maintenance Cell Survival Cell physiology Cells Chromosomes Chronic Cognition Complex Copy Number Polymorphism Data Dependency Development Diagnosis Disease Disease susceptibility Etiology Exons Family Fatigue Gene Expression Genes Genetic Grant Histocompatibility Homeostasis IL7R gene Immune Immune response In Vitro Individual Inflammation Inflammatory Interleukin-7 Light Maintenance Mediating Membrane Memory Messenger RNA Minor Molecular Molecular Analysis Multiple Sclerosis Muscle Weakness Myelin Nature Neuraxis Neurodegenerative Disorders Neurologic Neurologic Dysfunctions Pathology Pathway interactions Patients Peripheral Peripheral Blood Mononuclear Cell Play Population Predisposition Process Production Protein Isoforms Proteins RNA Splicing Receptor Gene Relapsing-Remitting Multiple Sclerosis Repression Research Rest Risk Role SNP genotyping Sensory Signal Pathway Signal Transduction Susceptibility Gene T cell differentiation T cell regulation T memory cell T-Lymphocyte Testing Trans-Activators Trans-Splicing Transcriptional Silencer Elements Transmembrane Domain United States Wheelchairs alpha chain interleukin-7 receptor base case control cohort cytotoxic disability experience genetic analysis genetic association genetic linkage analysis human TSLP protein in vivo novel outcome forecast pathogen protein expression public health relevance receptor binding response

项目摘要

DESCRIPTION (provided by applicant): Defining the functional role of a novel MS susceptibility gene, IL7R alpha chain. Multiple sclerosis (MS) is a debilitating neurodegenerative disorder of the central nervous system (CNS) that is thought to be mediated by T-cell autoimmunity and causes neurological inflammation and progressive neurological dysfunction. The `complex disease' nature of MS has made it difficult to identify genes implicated in, and understand the underlying molecular mechanisms of the disease. We have recently generated exciting new data which has identified significant association with MS of a SNP within the interleukin 7 alpha chain receptor gene (IL7R1). Further, we have proven that the associated SNP leads to increased skipping of the transmembrane domain of the protein, resulting in increased production of the soluble form of IL7R1. The objective of this grant is to build upon this ground breaking discovery. We propose to identify the cis- and trans- factors involved in exon 6 IL-7R1 splicing, determine the effect that exon skipping has upon interleukin 7 (IL-7) and thymic stromal lymphopoietin (TSLP) pathways, and the influences that this has upon naove T- cell differentiation and memory T-cell homeostasis. By elucidating these mechanisms we hope to gain a better understand IL7R1 is functionally implicated in the etiology of MS. PUBLIC HEALTH RELEVANCE: Multiple sclerosis (MS) is a debilitating neurodegenerative disorder of the central nervous system that affects more than 400,000 individuals in the United States. We have recently generated exciting new data in which have identified a gene (IL-7R) implicated in MS. This grant builds upon our discovery by investigating of the functional that the candidate gene plays in immune response and how this may contribute to MS. We propose to compare the function of IL-7R in specific immune cells in MS patients and control individuals to identify how IL-7R influences immune cell maintenance.

描述（由申请人提供）：定义一种新的MS易感基因IL7R α链的功能作用。多发性硬化症（MS）是一种中枢神经系统（CNS）的衰弱性神经退行性疾病，被认为是由t细胞自身免疫介导的，可引起神经炎症和进行性神经功能障碍。多发性硬化症的“复杂疾病”性质使得鉴定与该疾病有关的基因和了解其潜在的分子机制变得困难。我们最近获得了令人兴奋的新数据，发现了白细胞介素7 α链受体基因（IL7R1）中一个SNP与MS的显著关联。此外，我们已经证明，相关的SNP导致蛋白质跨膜结构域的跳跃增加，导致可溶性形式IL7R1的产生增加。这项拨款的目的是在这一突破性发现的基础上进一步发展。我们建议确定参与外显子6 IL-7R1剪接的顺式和反式因子，确定外显子跳跃对白细胞介素7 （IL-7）和胸腺基质淋巴生成素（TSLP）途径的影响，以及这对幼年T细胞分化和记忆T细胞稳态的影响。通过阐明这些机制，我们希望更好地了解IL7R1在MS病因学中的功能作用。