Regulation of microRNA processing

microRNA 加工的调控

• 批准号: 8630834
• 负责人: Gabriele Varani
• 金额: $ 28.32万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-01 至 2018-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8630834
• 关键词: 3' Untranslated Regions; Affect; Alternative Splicing; Alzheimer' s Disease; Binding; Binding Sites; Biochemical; Biogenesis; Biological Assay; Biological Process; Cell Death; Cell Extracts; Cell Line; Cell Nucleus; Cell Survival; Cell physiology; Cells; Cholesterol; Chronic Disease; Cleaved cell; Complex; Cyclic Peptides; Cytoplasm; Development; Dicer Enzyme; Disease Progression; Down-Regulation; Engineering; Family; Foxes; Functional RNA; Gene Expression; Gene Targeting; Genes; Genetic; Human; In Vitro; Individual; Lead; Lipoproteins; Malignant Neoplasms; Messenger RNA; MicroRNAs; Nucleotides; Oligonucleotides; Oncogenic; Peptides; Physiological; Plasma; Post-Transcriptional Regulation; Process; Production; Protein Engineering; Protein Family; Proteins; RNA Binding; RNA Precursors; RNA Recognition Motif; RNA Splicing; RNA-Binding Proteins; Regulation; Ribonuclease III; Therapeutic; Time; Transcript; analog; base; cancer cell; exportin 5; human DICER1 protein; human disease; improved; in vivo; inhibitor/antagonist; insulin sensitivity; mRNA Precursor; mRNA Stability; malignant breast neoplasm; mimetics; novel strategies; novel therapeutics; overexpression; pre-miRNA; pri-miRNA; public health relevance; stem; tumor progression

DESCRIPTION (provided by applicant): MicroRNAs represent a large class of non-coding RNAs that regulate gene expression by interacting with the 3'-untranslated region of target mRNAs. In addition to being essential regulators of development, differentiation and many other basic cellular processes, microRNA expression is associated with the progression of cancer and other chronic diseases, suggesting that regulation of specific microRNAs could have significant therapeutic benefits. Our objective is to investigate the mechanism by which pre-mRNA splicing factors regulate processing of a subset of miRNA precursors. Since we have also identified peptide mimetics that inhibit processing of an oncogenic miRNA (miR- 21) by the RNase III enzyme Dicer, we also propose to investigate the mechanism of inhibition of microRNA processing by this new class of molecules and to further develop their activity. We specifically propose to: 1) Study the regulation of microRNA processing by the Fox-1 family of splicing factors. We will investigate the structural and biochemical mechanism of regulation and the physiological consequences of downregulation of miR-20b expression by Fox-1 and Fox-2. 2) Study the structural and biochemical mechanism of inhibition of microRNA processing by a new class of peptide mimetics and by engineered RNA- binding proteins we have identified. 3) Improve the activity of the peptide inhibitors we have discovered. By conducting this project, we will investigate how processing of microRNA precursors is regulated by endogenous RNA-binding proteins and by exogenous inhibitors. This will provide information critical to understand post-transcriptional regulation of microRNA production, and new approach to inhibiting the activity of oncogenic microRNAs and to improve the potency of the inhibitors.

描述（由申请人提供）：microRNA代表一类非编码RNA，通过与靶mRNA的3'-非翻译区相互作用来调节基因表达。除了是发展的必要调节因子，分化和许多其他基本细胞过程外，MicroRNA表达与癌症和其他慢性疾病的进展有关，这表明对特定microRNA的调节可能具有显着的治疗益处。 我们的目的是研究MRNA前剪接因子调节miRNA前体的处理的机制。由于我们还确定了RNASE III酶dicer抑制抑制致癌miRNA（miR-21）的肽模拟物，因此我们还建议研究这种新的分子抑制microRNA加工的机制，并进一步发展其活性。我们特别提出：1）研究FOX-1剪接因子家族对microRNA处理的调节。我们将研究调节的结构和生化机制以及FOX-1和FOX-2对miR-20b表达下调的生理后果。 2）研究新型肽模拟物和我们已经确定的工程RNA结合蛋白抑制microRNA加工的结构和生化机制。 3）改善我们发现的肽抑制剂的活性。通过进行该项目，我们将研究MicroRNA前体的加工如何受内源性RNA结合蛋白和外源抑制剂的调节。这将提供关键的信息，以了解microRNA产生的转录后调节，以及抑制致癌微RORNA活性并提高抑制剂效力的新方法。