Myotonic Dystrophy: Molecular Pathophysiology and CNS Effects

强直性肌营养不良：分子病理生理学和中枢神经系统影响

• 批准号: 8305703
• 负责人: Laura P.W Ranum
• 金额: $ 119.84万
• 依托单位: UNIVERSITY OF FLORIDA
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-15 至 2013-09-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8305703
• 关键词: Affect; Behavior; Binding Proteins; Brain; Child; Chromosomes, Human, Pair 19; Chromosomes, Human, Pair 3; Consensus; Defect; Development; Disease; Endocrine system; Eye; Family member; Functional disorder; Generations; Genes; Genetic Transcription; Goals; Heart; Hereditary Disease; Image; Introns; Lead; Learning; Magnetic Resonance Imaging; Mediating; Mental Retardation; Microsatellite Repeats; Molecular; Muscle; Muscular Dystrophies; Mutation; Myotonic Dystrophy; Neuraxis; Neuropsychological Tests; Pathogenesis; Patients; Pattern; Personality; Protein Kinase; RNA; RNA-Binding Proteins; Reporting; Research Personnel; Resolution; Skeletal Muscle; Sleep; Transcript; clinically significant; disease-causing mutation; executive function; gain of function; interdisciplinary approach; molecular pathology; mouse model; neuropathology; optical imaging; programs

Myotonic dystrophy type 1 (DM1) is caused by a CTG expansion mutation located in the 3' untranslated portion of the dystrophica myotonica protein kinase gene. The identification and characterization of RNA-binding proteins that interact with expanded CUG repeats and the discovery that a similar transcribed but untranslated CCTG expansion in an intron causes myotonic dystrophy type 2 (DM2), have uncovered a new type of mechanism in which microsatellite expansion mutations cause disease through an RNA gain of function mechanism in which CUG and CCUG expansion transcripts lead to the dysregulation of key RNA-binding proteins, including muscleblind (MbnH) and CUG-binding protein (CUG-BP), which in turn lead to the downstream dysregulation of specific set of genes that cause the multisystemic features common to both diseases. Although the CNS deficits are one of the most clinically significant aspects of DM, the molecular mechanisms underlying these changes are unclear. Only DM1 causes developmental defects, including mental retardation, but both forms of DM result in degenerative CNS effects that have not yet been well characterized. The focus of this proposal is to characterize the CNS effects of the DM1 and DM2 mutations in patients through imaging studies and neuropsychological testing and to relate these changes to the underlying molecular deficits through the generation and characterization of mouse models. To accomplish these goals the following Projects and Cores are proposed as part of our overall Program entitled: Myotonic Dystrophy: Molecular Pathophysiology and CNS Effects. Project 1: Temporal/spatial RNA expression effects in DM1 and DM2 Project 2: Mechanisms of RNA-Mediated CNS Pathogenesis in Myotonic Dystrophy Project 3: Structural and Functional CNS Changes in Children with Myotonic Dystrophy Type 1 Core A: Neuropathology and Optical Imaging Core Core B: Administrative Core

强直性肌营养不良1型（DM 1）是由位于肌营养不良症蛋白激酶基因3'非翻译部分的CTG扩增突变引起的。与扩增的CUG重复序列相互作用的RNA结合蛋白的鉴定和表征，以及发现内含子中类似的转录但未翻译的CCTG扩增导致强直性肌营养不良2型（DM 2），发现了一种新的机制，其中微卫星扩增突变通过RNA获得功能机制引起疾病，其中CUG和CCUG扩增转录本导致关键RNA的失调，结合蛋白，包括肌盲（MbnH）和CUG结合蛋白（CUG-BP），这反过来又导致下游的一组特定基因的失调，导致两种疾病共同的多系统特征。虽然中枢神经系统的缺陷是糖尿病的最重要的临床方面之一，这些变化的分子机制尚不清楚。只有DM 1会导致发育缺陷，包括智力迟钝，但这两种形式的DM导致退行性CNS效应，尚未得到很好的表征。该提案的重点是通过影像学研究和神经心理学测试表征患者中DM 1和DM 2突变的CNS效应，并通过小鼠模型的生成和表征将这些变化与潜在的分子缺陷联系起来。为了实现这些目标，以下项目和核心建议作为我们的整体计划的一部分，题为：强直性肌营养不良症：分子病理生理学和中枢神经系统的影响。 项目1：DM 1和DM 2中的时间/空间RNA表达效应 项目2：强直性肌营养不良中RNA介导的CNS发病机制 项目3：1型肌强直性营养不良儿童的结构和功能CNS变化 核心A：神经病理学和光学成像核心 核心B：行政核心