The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome

剪接体对核前信使RNA剪接的催化机制

• 批准号: 9276215
• 负责人: Joseph Anthony Piccirilli
• 金额: $ 22.53万
• 依托单位: UNIVERSITY OF CHICAGO
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-24 至 2018-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9276215
• 关键词: Achievement; Address; Affect; Architecture; Binding; Binding Sites; Biochemistry; Biological Assay; Biology; Bypass; Catalysis; Catalytic Domain; Catalytic RNA; Cells; Chemicals; Chemistry; Collaborations; Defect; Dimensions; Disease; Docking; Enzymes; Eukaryota; Evolution; Gene Expression; Genes; Genetic Transcription; Goals; Health; Human; Individual; Introns; Investigation; Ions; Left; Mediating; Metals; Modeling; Molecular Genetics; Mutation; Nuclear; Pathway interactions; Play; Positioning Attribute; Proteins; Proteome; RNA; RNA Splicing; Regulation; Resolution; Role; Site; Small Nuclear RNA; Spliceosomes; Staging; Structure; System; Testing; Translations; Work; base; catalyst; divalent metal; endonuclease; human disease; inorganic phosphate; insight; mRNA Precursor; meetings; novel; reconstitution; scaffold; treatment strategy

DESCRIPTION (provided by applicant): Our long-term goal is to elucidate the mechanisms by which the spliceosome catalyzes pre-mRNA splicing and in particular to define the structural and functional role of RNA and protein in catalysis. Catalysis of pre-mRNA splicing by the spliceosome is a defining feature of eukaryotes. In humans, catalysis is required to excise ten introns on average for nearly every gene, and catalysis at alternative sites expands the proteome and contributes to the complexity of higher eukaryotes. Indeed, mutations in at least 15% of human diseases result from errors in splicing. Despite this importance of pre-mRNA splicing to eukaryotic gene expression, for decades our understanding of splicing catalysis has languished, particularly in comparison to our understanding of catalysis at the two other major stages of gene expression - transcription and translation. We have not even known whether catalysis is mediated by the RNA or protein parts of the spliceosome. However, through our collaborative efforts, we have recently provided definitive evidence that the RNA parts catalyze splicing, positioning two divalent metal ions for interaction with the scissile phosphates. Strikingly, our work also establishes that the spliceosome utilizes a catalytic mechanism indistinguishable from the catalytic mechanism of self-splicing group II RNA introns, extending the parallels with the group II intron to the atomic level at the catalytic core and providing strog support for the hypothesis that these two enzymes share common evolutionary origins. Despite this advance and other achievements in the field, many fundamental questions remain. For example, how are the nucleophiles in either splicing system activated for catalysis, how does the architecture of the spliceosomal catalytic core position the reactive sites for catalysis, and what is the role of protein in mediating RNA-based catalysis? To answer these questions, we aim to test a metal cluster model for catalysis of nuclear pre-mRNA splicing, to define the architecture and dynamics of the catalytic core of the spliceosome, and to define the essential role of protein in assisting RNA-based splicing catalysis. We will accomplish these aims through a continuation of our unique and synergistic collaboration that allows for a combined approach of chemistry, biochemistry and molecular genetics. This work will transform our understanding of the roles of RNA and protein in spliceosomal catalysis, with significant implications for understanding the origins and evolution of the spliceosome.

描述（由申请人提供）：我们的长期目标是阐明剪接体催化前mRNA剪接的机制，特别是定义RNA和蛋白质在催化中的结构和功能作用。剪接体对前 mRNA 剪接的催化是真核生物的一个决定性特征。在人类中，几乎每个基因平均需要催化作用来切除十个内含子，而替代位点的催化作用会扩展蛋白质组并增加高等真核生物的复杂性。事实上，至少 15% 的人类疾病的突变是由剪接错误造成的。尽管mRNA前体剪接对于真核基因表达非常重要，但几十年来，我们对剪接催化的理解一直处于停滞状态，特别是与我们对基因表达的另外两个主要阶段（转录和翻译）催化的理解相比。我们甚至不知道催化作用是由剪接体的RNA还是蛋白质部分介导的。然而，通过我们的合作努力，我们最近提供了明确的证据，证明 RNA 部分催化剪接，定位两个二价金属离子与可裂解的磷酸盐相互作用。引人注目的是，我们的工作还证实剪接体利用了与自剪接 II 族 RNA 内含子的催化机制无法区分的催化机制，将与 II 族内含子的相似之处扩展到催化核心的原子水平，并为该假设提供了强有力的支持。这两种酶具有共同的进化起源。尽管该领域取得了这一进展和其他成就，但仍然存在许多基本问题。例如，任一剪接系统中的亲核试剂如何被激活以进行催化，剪接体催化核心的结构如何定位催化反应位点，以及蛋白质在介导基于RNA的催化中的作用是什么？为了回答这些问题，我们的目标是测试用于核前mRNA剪接催化的金属簇模型，定义剪接体催化核心的结构和动力学，并定义蛋白质在协助基于RNA的剪接中的重要作用催化。我们将通过继续我们独特的协同合作来实现这些目标，这种合作允许化学、生物化学和分子遗传学的综合方法。这项工作将改变我们对 RNA 和蛋白质在剪接体催化中的作用的理解，对于理解剪接体的起源和进化具有重要意义。