Processing of Pre-Messenger RNA

前信使 RNA 的加工

• 批准号: 6613433
• 负责人: SUSAN M BERGET
• 金额: $ 48.92万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 1988
• 资助国家: 美国
• 起止时间: 1988-04-01 至 2006-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6613433
• 关键词: RNA binding protein; RNA splicing; cell line; gene induction /repression; genetic enhancer element; genetic regulation; genetic regulatory element; helicase; introns; laboratory rat; nucleic acid biosynthesis; nucleic acid sequence; precursor mRNA; protein binding; protein protein interaction; protein purification; spliceosomes; transcription factor

DESCRIPTION (provided by applicant): Alternative pre-mRNA splicing contributes significantly to genetic diversity in vertebrates. This proposal is aimed at understanding the mechanisms underlying the regulation of alternative pre-mRNA splicing. Alternatively spliced regions of a pre-mRNA are characterized by the presence of splicing enhancer or silencer sequence elements recognized by splicing factors. Our work concentrates on four systems of pre-mRNA splicing that involve different types of regulatory elements and splicing factors. Included in the RNA regulatory sequence elements to be studied are: 1) C/A-rich exon enhancers that stimulate exon inclusion, G/A-rich exon enhancers that stimulate exon inclusion and regulate 5' splice site usage, G-rich intron enhancers that regulate 5' splice site usage, and C-rich intron elements that stimulate splicing and spliceosome assembly. Experiments are described to: 1) continue characterization of the factors that recognize these RNA elements, 2) identify and characterize factors that recognize element-binding factors to regulate splicing, 3) determine the role of RNA helicases in alternative splicing and 4) investigate the hypothesis that alternative splicing and transcriptional elongation are linked.

描述（由申请人提供）：前体mRNA的选择性剪接对脊椎动物的遗传多样性有重要贡献。该建议旨在了解替代性前mRNA剪接的调节机制。前体mRNA的选择性剪接区的特征在于存在剪接因子识别的剪接增强子或沉默子序列元件。我们的工作集中在四个系统的前mRNA剪接，涉及不同类型的调控元件和剪接因子。待研究的RNA调控序列元件包括：1）刺激外显子包含的富含C/A的外显子增强子，刺激外显子包含并调控5'剪接位点使用的富含G/A的外显子增强子，调控5'剪接位点使用的富含G的内含子增强子，以及刺激剪接和剪接体组装的富含C的内含子元件。实验描述为：1）继续鉴定识别这些RNA元件的因子，2）鉴定和鉴定识别元件结合因子以调节剪接的因子，3）确定RNA解旋酶在选择性剪接中的作用，以及4）研究选择性剪接和转录延伸相关联的假设。