Protein RNA Rearrangements in the Spliceosome

剪接体中蛋白质 RNA 重排

• 批准号: 7259452
• 负责人: CHARLES C QUERY
• 金额: $ 38.71万
• 依托单位: ALBERT EINSTEIN COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-08-01 至 2008-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7259452
• 关键词: 3' Splice Site; ATP phosphohydrolase; ATPase Domain; Active Sites; Affinity; Alleles; Alternative Splicing; Binding; Biochemical; Catalytic Domain; Chemicals; Class; Code; Complement; Complex; DDX16 Gene; DNA Sequence Rearrangement; Decompression Sickness; Development; Event; Excision; Exons; Family; Figs - dietary; Fission Yeast; Gene Expression; Genetic; Genetic Screening; Genetic Transcription; Goals; Hela Cells; Heterogeneous Nuclear RNA; Human; Individual; Infection; Introns; Investigation; Ligands; Link; Mediating; Modification; Molecular Conformation; Mutate; Mutation; Nucleotides; Pathway interactions; Pattern; Polyadenylation; Process; Proteins; RNA; RNA Splicing; Reaction; Relative (related person); Research Personnel; Role; Saccharomyces cerevisiae; Scheme; Screening procedure; Site; Spliceosome Assembly Pathway; Spliceosomes; Substrate Interaction; System; U2 Small Nuclear Ribonucleoprotein; U6 small nuclear RNA; Yeasts; comparative; falls; helicase; improved; in vivo; mRNA Precursor; mutant; programs; research study; tumorigenesis

DESCRIPTION (provided by applicant): Excision of introns from precursor messenger RNA by the spliceosome is a critical step in almost all human gene expression. This process is highly regulated, integrally linked with the transcription of genes and other processing events, such as polyadenylation and nucleotide modification. A better understanding of pre-mRNA splicing will be essential to further understand mechanisms that regulate splicing, that control patterns of alternative splicing, and that contribute to development, oncogenesis and retroviral infections. The mechanism by which the spliceosome recognizes the exact sites for the chemical events and how he reactions are catalyzed are not well understood. The long-term goals of this project are to understand interactions and rearrangements between spliceosome components and the RNA ligands that are substrates for the catalytic reactions. Ample evidence argues for multiple rearrangements of factors and multiple recognition events at the branch site. Investigation of these events -- which are not understood mechanistically -- will elucidate interactions and rearrangements among core components and may serve as a paradigm for other rearrangements and multiple recognition events that occur elsewhere in the spliceosome. This proposal focuses first on the first ATP-dependent step of spliceosome assembly - the stable binding of U2 snRNP around the branch region, and investigates the action of an ATPase, Prp5. As the first ATP-dependent event, this step provides a uniquely simplified system, for studying the action of a spliceosomal ATPase. Further experiments will focus on the mechanism and the consequences of a recently identified bridging interaction between U1 and U2 snRNPs that is mediated by Prp5. Finally, using a new genetic screen, we are investigating interactions between the branch site (and the 5' and 3' splices sites) and components of the spliceosome critical for the second catalytic reaction, interactions between the identified components and the RNA substrate, and interactions of the identified components with other constituents of the spliceosome -- with a particular bent as to mechanism by which these components interact to help juxtapose the reactants for the second chemical step.

描述（由申请人提供）：剪接体从前体信使RNA中切除内含子是几乎所有人类基因表达的关键步骤。这一过程受到高度调控，与基因转录和其他加工事件（如聚腺苷酸化和核苷酸修饰）紧密相关。更好地了解pre-mRNA剪接对于进一步理解调节剪接的机制、控制可选剪接模式以及促进发育、肿瘤发生和逆转录病毒感染至关重要。