Transcription mechanism of Myrf for central nervous system myelination

Myrf对中枢神经系统髓鞘形成的转录机制

• 批准号: 9384786
• 负责人: YUNGKI PARK
• 金额: $ 3.39万
• 依托单位: STATE UNIVERSITY OF NEW YORK AT BUFFALO
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-01-01 至 2019-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9384786
• 关键词: Adult; Applications Grants; Binding; Biogenesis; Bioinformatics; Biological Assay; Cell Line; Cell Nucleus; ChIP-seq; Cleaved cell; Collaborations; Computer Analysis; Cues; DNA; Data; Development; Endoplasmic Reticulum; Genetic Transcription; Genetic study; Homo; Immunofluorescence Immunologic; Immunoprecipitation; Impairment; In Vitro; Investigation; Laboratories; Learning; Life; Link; Luciferases; Maintenance; Mass Spectrum Analysis; Mediating; Membrane; Membrane Proteins; Modeling; Molecular; Molecular Chaperones; Mus; Mutagenesis; Myelin; N-terminal; Names; Nature; Neuraxis; Oligodendroglia; Phenotype; Proteolysis; Publishing; Regulation; Role; Small Interfering RNA; Specificity; Stimulus; Sum; Tertiary Protein Structure; Thick; Transcriptional Regulation; Western Blotting; Work; chromatin protein; combinatorial; experimental analysis; experimental study; myelination; nervous system disorder; neuropsychiatric disorder; notch protein; novel; protein complex; public health relevance; transcription factor

 DESCRIPTION (provided by applicant): Myelination of the central nervous system (CNS) by oligodendrocytes (OLs) is essential for the development and function of the CNS. Myelin develops in the CNS as OLs differentiate into the myelin-forming mature phenotype. The differentiation of OLs is under tight regulation, and its dysregulation causes neurological disorders and has been linked to neuropsychiatric diseases. Genetic studies have shown that Myrf is a key transcription factor for the development and life-long maintenance of myelin in the CNS. Recent studies have also demonstrated that Myrf is critical to the fine-tuning of myelin thickness and its plasticity that underlies learning in the adult stage. Despite these crucial role, it remains poorly understood how Myrf regulates transcription, and this significantly impedes the progress in this field. Using bioinformatics and experimental approaches, we recently made the breakthrough observations that Myrf is a membrane-bound transcription factor, and that Myrf may function as a homo-trimeric transcription factor. Membrane-bound transcription factors are generated as membrane proteins that, upon relevant stimuli, undergo proteolytic activation to release transcription factor domains from the membrane, with Notch being the most famous example. Our discovery fundamentally changes the paradigm for Myrf, providing a powerful framework to understand its functional mechanism. Building upon this discovery, Aim I will elucidate how Myrf is activated by proteolysis. The proteolytic activation of Myrf releases its N-terminal fragment from the membrane, allowing it to translocate into the nucleus for transcriptional regulation. Aim II will determine how the N-terminal fragment of Myrf interacts with DNA as a homo-trimer for transcription. Our computational and experimental analyses indicate that functional collaboration with other transcription factors is critical to the transcriptional activity of Myrf. Aim III will elucidate which transcription factors interact with yrf for coordinated differentiation of OLs. In sum, this study will elucidate the transcription mechanism of Myrf for OL differentiation and CNS myelination.