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Characterization of functional molecular domains of MeCP2

MeCP2 功能分子结构域的表征

基本信息

批准号：
10459358
负责人：
Bridget E Collins
金额：
$ 4.6万
依托单位：
VANDERBILT UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-08-01 至 2023-05-12
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10459358
关键词：
Address Adverse effects Affect Affinity Age Aggressive behavior Alleles Behavioral Binding Biological Assay Brain Brain region C-Terminal Binding Protein 2 C-terminal Cell model Cells Chromatin Communication Communities Complement Complementary DNA Complex Critical Thinking DNA DNA Binding Data Development Disease Disease model Dissection Environment Fellowship Functional disorder Gene Expression Genes Genetic Genetic Engineering Genetic Transcription Goals Hand High Prevalence In Vitro Individual Institutes Investigation Life Link MeCP2 Duplication Syndrome Methyl-CpG-Binding Protein 2 Missense Mutation Molecular Molecular Conformation Movement Mus Mutation Neurodevelopmental Disorder Overlearning Pathogenicity Patients Pediatric Neurology Phenotype Physiological Plasmids Point Mutation Proteins Reader Repressor Proteins Research Research Training Rett Syndrome Risk Severity of illness Speech System Technical Expertise Therapeutic Time Training Transgenic Organisms Work autistic clinical decision-making clinically relevant conditioned fear disability disease-causing mutation falls gain of function gain of function mutation gene therapy genetic corepressor girls in vivo innovation insight loss of function loss of function mutation molecular domain mouse model mutant novel novel therapeutic intervention pediatric department precision medicine preservation protein function restoration skills

项目摘要

PROJECT SUMMARY/ABSTRACT Rett syndrome, an X-linked neurodevelopmental disorder caused predominantly by mutations in the gene encoding chromatin modulator Methyl-CpG-binding protein 2 (MECP2), is a leading genetic cause of disability in girls worldwide. Affected individuals develop typically for a period of 6-18 months, at which time the disease causes developmental regression with loss of purposeful hand movements, loss of speech, and autistic features. Treatment options are currently limited to symptomatic management, making the development of novel therapeutic approaches critically important. 10% of disease-causing MECP2 mutations arise in its C- terminal domain. However, despite the high prevalence of mutations in this region, few studies have investigated their pathophysiological mechanism(s). Furthermore, proposed therapeutic strategies for RTT focus largely on remedying loss-of-function (LOF) mutations that occur in other domains of MeCP2 - the methyl-binding and NCoR-interaction domains. Previous work suggests that the C-terminus may alter local chromatin binding and conformation, but thorough functional studies of different types of C-terminal mutations are lacking. Preliminary data shows that one of the most common C-terminal mutations that eliminates the entire domain, R294X, yields a truncated protein product in mice that accumulates with age and binds chromatin more tightly than wild-type MeCP2, suggesting that the R294X mutation may not act through simple LOF. With the resulting hypothesis that some C-terminal mutations cause Rett syndrome via a non-LOF mechanism, this proposal aims to 1) determine the contributions of the MeCP2 C-terminus to protein function as a transcriptional modulator, 2) elucidate how the R294X mutation elicits transcriptional dysregulation in three different brain regions, and 3) establish the behavioral consequences of transgenic complementation of the R294X allele. The proposed studies will involve the development of an in vitro framework to probe C- terminal Mecp2 mutations in functional assays for chromatin binding and co-repressor interaction, as well as the use of dual molecular and behavioral approaches to dissect the pathogenic mechanism of the prevalent R294X mutation. This research will provide mechanistic insight into the complex neurodevelopmental disorder Rett syndrome, as well as assist clinical decision-making by identifying the viability of proposed therapies for individuals with C-terminal MECP2 mutations. The proposed research will be accomplished through a carefully crafted fellowship training plan that involves opportunities to develop the applicant's technical expertise, critical-thinking skills, and scientific communication skills. Further, the research environment provided in turns by the MSTP, Vanderbilt Brain Institute, and Department of Pediatric Neurology is ideal for the proposed research and training, harboring a reputation for scientific excellence, a collegial community, and a strong focus on trainee development.

项目摘要/摘要 Rett综合征，一种主要由基因突变引起的X连锁神经发育障碍编码染色质调节剂甲基CpG结合蛋白2(MECP2)是导致残疾的主要遗传原因在世界各地的女孩中。受影响的个体通常发展为6-18个月，此时疾病导致发育衰退，失去有目的的手部动作、言语障碍和自闭症功能。目前的治疗选择仅限于对症治疗，这使得新的治疗方法至关重要。10%的致病基因MECP2突变发生在其C- 终端域。然而，尽管该区域突变的发生率很高，但很少有研究探讨了它们的病理生理机制(S)。此外，针对RTT提出了治疗策略主要关注于补救发生在MeCP2其他区域的功能丧失(LOF)突变-The 甲基结合区域和NCoR-相互作用区域。以前的工作表明，C-末端可能会改变局部染色质结合和构象，但对不同类型的C末端突变进行全面的功能研究都是缺乏的。初步数据显示，最常见的C末端突变之一消除了整个结构域R294X在小鼠体内产生一种截短的蛋白质产物，该产物随着年龄的增长而积累并结合染色质比野生型MeCP2更紧密，表明R294X突变可能不是通过简单的洛夫。由此产生的假设是某些C末端突变通过非LOF导致Rett综合征机制，本建议旨在1)确定MeCP2 C末端对蛋白质功能的贡献作为一种转录调节因子，2)阐明R294X突变是如何在三个不同的大脑区域，以及3)建立转基因互补的行为后果 R294X等位基因。拟议的研究将涉及开发一种体外框架来探索C- 染色质结合和共抑制物相互作用功能分析中的末端MeCP2突变，以及用双重分子和行为学方法剖析流行肺炎的发病机制 R294X突变。这项研究将为复杂的神经发育障碍提供机械学上的见解。 Rett综合征，以及通过确定拟议的治疗方法的可行性来辅助临床决策具有C-末端MECP2突变的个体。拟议的研究将通过仔细的精心设计的奖学金培训计划，包括发展申请人的技术专长的机会；批判性思维能力和科学沟通能力。此外，研究环境轮流提供由MSTP、范德比尔特脑研究所和儿科神经科提出的理想建议研究和培训，拥有卓越的科学声誉，大学社区和强大的注重实习生发展。