Characterization of the mRNP closed-loop structure

mRNP 闭环结构的表征

• 批准号: 8496294
• 负责人: CLYDE L DENIS
• 金额: $ 33.12万
• 依托单位: UNIVERSITY OF NEW HAMPSHIRE
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-06-15 至 2017-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8496294
• 关键词: Affinity Chromatography; Animal Model; Binding; Biochemical; Biological; Biological Sciences; Cell Nucleus; Charge; Complex; Coupled; Cytoplasmic Granules; Data; Defect; Detection; Disease; Eukaryota; Event; Fluorescence; Genetic Transcription; Glucose; Goals; Grant; Immunoprecipitation; Individual; Initiator Codon; Investigation; Light; Link; Macromolecular Complexes; Mass Chromatography; Mass Spectrum Analysis; Messenger RNA; Methionine; Modeling; Mutation; Nature; Nuclear; Peptide Initiation Factors; Play; Poly(A) Tail; Poly(A)-Binding Protein I; Process; Production; Protein Binding; Protein Biosynthesis; Proteins; Public Health; RNA; RNA Cap-Binding Proteins; Recycling; Regulation; Research; Resort; Ribosomes; Role; Saccharomyces cerevisiae; Scanning; Shapes; Stress; Structural Protein; Structure; Study models; Sucrose; Suggestion; System; Systems Analysis; Techniques; Terminator Codon; Time; Training; Transfer RNA; Translation Initiation; Translational Repression; Translations; Yeasts; analytical ultracentrifugation; biological systems; graduate student; mRNA Export; macromolecular assembly; messenger ribonucleoprotein; novel; protein complex; protein expression; public health relevance; termination factor; tool; undergraduate student

DESCRIPTION (provided by applicant): The goal of these studies is to use the novel technique of analytical ultracentrifugation with fluorescence detection system (AU-FDS) to analyze translation complexes by detecting specific GFP- tagged proteins and mRNA. AU provides real-time analysis of the size of complexes using various wavelengths to identify biological molecules. It provides enhanced precision as to the actual size of complexes and avoids the inexactitude and the time-intensive nature inherent in secondary Western and Northern analysis. Importantly, AU-FDS allows the identification of macromolecular complexes that have not previously been visualized by standard techniques. Most critically, while other immunoprecipitation studies indicate that proteins interact, AU-FDS studies take this research to the next logical step: identifying the number, size, and composition of these protein complexes. Previously, we have used AU-FDS analysis coupled with an affinity purification of a Flag- tagged translational component (Flag-PAB1 or RPL25A-Flag) to identify from the yeast S. cerevisiae a 77S monosomal translation complex that contained mRNA, the closed-loop structural components, eIF4E, eIF4G, PAB1, and the 80S ribosome. In expansion of these studies we have used affinity purification of translation termination factor, Flag-eRF1, to identif four novel complexes, 21S, 28S, 38S, and 77S in size. The 21S/28S complexes (about 0.5 to 1.4 MDa depending on their shape) contained at least eRF1, eIF4E, eIF4G1, PAB1, HRP1, and mRNA. Many common stress granule proteins and eIF2 and eIF5 initiation factors were not present in the 21S/28S complexes. Our data suggest that the 21S/28S complexes are similar to the putative closed-loop mRNP structure. This model is consonant with the recent suggestion that HRP1 plays a role in transitioning mRNA, newly imported from the nucleus, into a translatable form. Alternatively, these complexes could be post- termination mRNP structures. In this grant we shall use the complementary techniques of AU-FDS and mass spectrometry to identify all of the components of the 21S/28S complexes. These studies will inform as to which translation initiation components, translation termination factors, and/or stress granule proteins are present in the complexes. Specific mutations in transcription, mRNA export, translation initiation, termination, and P body/stress granule formation will be used to identify at which step these Flag- eRF1 complexes are functioning. In addition, we will use a number of defined mutations in eIF4E, eIF4G, and PAB1 to investigate the structure and shape of the putative closed-loop mRNPs. Finally, the exact translational complexes bound by translational repressors, SBP1, SCD6, and NPL3, will be determined by AU-FDS using Flag-tagged versions of PAB1, eIF4E, and eRF1.

描述(申请人提供)：这些研究的目标是使用分析超速离心荧光检测系统(AU-FDS)的新技术，通过检测特定的GFP标记的蛋白质和mRNA来分析翻译复合体。AU使用不同的波长对复合体的大小进行实时分析，以识别生物分子。它提高了复合体实际大小的精确度，避免了二级西方和北方分析中固有的不准确和时间密集的性质。重要的是，AU-FDS允许识别以前没有通过标准技术可视化的大分子络合物。最关键的是，虽然其他免疫沉淀研究表明蛋白质相互作用，但AU-FDS研究将这项研究带入了下一个合乎逻辑的步骤：确定这些蛋白质复合体的数量、大小和组成。此前，我们已经使用AU-FDS分析结合Flag标记的翻译成分(Flag-PAB1或RPL25A-Flag)的亲和纯化来从酿酒酵母中鉴定出一个77S单体翻译复合体，它包含mRNA、闭环结构成分、eIF4E、eIF4G、PAB1和80S核糖体。在这些研究的扩展中，我们使用翻译终止因子Flag-eRF1的亲和纯化来鉴定四个新的复合物，大小分别为21S、28S、38S和77S。21S/28S复合体至少含有eRF1、eIF4E、eIF4G1、PAB1、HRP1和mRNA。在21S/28S复合体中不存在许多常见的应激颗粒蛋白和eIF2和eIF5启动因子。我们的数据表明，21S/28S复合体类似于假定的闭环mRNP结构。这一模型与最近的建议是一致的，即HRP1在将新从细胞核输入的mRNA转化为可翻译形式方面发挥了作用。或者，这些复合体可以是终止后的mRNP结构。在这笔赠款中，我们将使用AU-FDS和质谱学的互补技术来鉴定21S/28S复合体的所有成分。这些研究将告知在复合体中存在哪些翻译起始成分、翻译终止因子和/或应激颗粒蛋白。在转录、信使核糖核酸输出、翻译起始、终止和P小体/应激颗粒形成中的特定突变将被用来确定这些Flag-eRF1复合体在哪一步发挥作用。此外，我们将使用eIF4E、eIF4G和PAB1中的一些已定义的突变来研究可能的闭环mRNPs的结构和形状。最后，由翻译抑制子SBP1、SCD6和NPL3结合的确切翻译复合体将由AU-FDS使用PAB1、eIF4E和eRF1的标记版本来确定。