Elucidating the Relations of Heat Shock Factors, Molecular Chaperones and Prions

阐明热休克因子、分子伴侣和朊病毒的关系

基本信息

批准号：
7467208
负责人：
LIMING LI
金额：
$ 31.14万
依托单位：
NORTHWESTERN UNIVERSITY AT CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-02-01 至 2013-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7467208
关键词：
Affect Alleles Anabolism Animal Model Anxiety Biology Bovine Spongiform Encephalopathy Cells Chronic Complex Condition Creutzfeldt-Jakob Syndrome Data Development Epidemic Equilibrium Etiology Future Gene Targeting Genes Genetic Screening Goals Heat shock proteins Heat-Shock Response Light Link Maintenance Microarray Analysis Molecular Molecular Chaperones Molecular Conformation Mutation Neurodegenerative Disorders Phenotype Play Prion Diseases Prions Process Protein Structure Initiative Protein-Folding Disease Proteins Public Health Publishing Regulation Reporting Research Role Saccharomyces cerevisiae Saccharomycetales Stress Testing Variant Wasting Syndrome Yeasts conformational conversion drug discovery genetic analysis heat shock transcription factor mutant novel novel therapeutics polypeptide prion hypothesis protein folding success

项目摘要

DESCRIPTION (provided by applicant): Despite decades of scientific research and heightening public and governmental anxiety over the potential dangers of infectious proteins and their role in epidemics such as new variant Creutzfeldt-Jacob disease, Mad Cow disease, and chronic Wasting disease, the mechanisms responsible for the conversion of a normal cellular protein into an infectious prion protein continue to defy understanding. The cellular factors instrumental to the protein conformational changes that result in prion formation, as well as those factors necessary for the subsequent stabilization of the altered prion conformation, remain a mystery. Considering that prion formation and inheritance are tightly related to the protein folding machinery, we propose to investigate the link between prion formation and heat shock transcriptional factors (HSFs). HSFs are evolutionally conserved transcriptional factors responsible for the biosynthesis of the majority of molecular chaperones, which are essential for protecting cells from extreme harsh conditions by refolding or dis-aggregating denatured proteins produced during the stress. Several molecular chaperones are also shown to play essential roles in prion propagation. Using the budding yeast Saccharomyces cerevisiae as the model organism, we propose to elucidate the relationship between HSFs and prion formation/propagation. Our long-term goal of the proposed research is to identify protein factors whose functions are regulated by HSFs and are essential for prion formation/propagation. The specific aims are: 1) to examine the regulatory role of heat shock protein 90kDa (Hsp90) complex in de novo formation and "strain" maintenance of [PSI+]; 2) to test if HSF and Hsp90 complex regulate other yeast prions. We will investigate if the effects of HSF and Hsp90/cochaperones are [PSI+] specific: 3) to identify additional novel factors that are HSF targets and responsible for prion formation and propagation. PUBLIC HEALTH RELEVANCE: Prion diseases are a group of infectious neurodegenerative diseases also known as transmissible spongiform encephalopathies. The molecular mechanisms govern the etiology of prion diseases are poorly understood. We propose to identify cellular factors that are required for prion conformational conversion and are important for subsequent stabilization of the acquired prion conformation. The success of proposed study will likely provide target genes for future drug discovery and new therapeutics for the devastating prion diseases.

描述（由申请人提供）：尽管经过数十年的科学研究，公众和政府对传染性蛋白质的潜在危险及其在新变种克雅氏病、疯牛病和慢性消耗性疾病等流行病中的作用的担忧日益加剧，但其机制负责将正常细胞蛋白转化为传染性朊病毒蛋白的机制仍然难以理解。有助于导致朊病毒形成的蛋白质构象变化的细胞因素，以及随后稳定改变的朊病毒构象所必需的因素，仍然是一个谜。考虑到朊病毒的形成和遗传与蛋白质折叠机制密切相关，我们建议研究朊病毒的形成和热休克转录因子（HSF）之间的联系。 HSF 是进化上保守的转录因子，负责大多数分子伴侣的生物合成，这对于通过重折叠或解聚应激过程中产生的变性蛋白质来保护细胞免受极端恶劣条件的影响至关重要。一些分子伴侣也被证明在朊病毒传播中发挥重要作用。使用芽殖酵母酿酒酵母作为模型生物，我们建议阐明 HSF 与朊病毒形成/传播之间的关系。我们拟议研究的长期目标是确定其功能受 HSF 调节且对朊病毒形成/传播至关重要的蛋白质因子。具体目标是： 1) 检查热休克蛋白 90kDa (Hsp90) 复合物在 [PSI+] 的从头形成和“应变”维持中的调节作用； 2) 测试HSF和Hsp90复合物是否调节其他酵母朊病毒。我们将研究 HSF 和 Hsp90/共伴侣蛋白的影响是否具有 [PSI+] 特异性：3) 确定作为 HSF 目标并负责朊病毒形成和传播的其他新因子。公共卫生相关性：朊病毒病是一组传染性神经退行性疾病，也称为传染性海绵状脑病。控制朊病毒疾病病因的分子机制尚不清楚。我们建议鉴定朊病毒构象转化所需的细胞因子，并且对于随后获得的朊病毒构象的稳定非常重要。拟议研究的成功可能会为未来的药物发现和毁灭性朊病毒疾病的新疗法提供靶基因。