The Trinucleotide Repeat Containing 6a-Mediated miRNA Activities in the Ciliogenesis of Airway Epithelium

含有 6a 的三核苷酸重复介导的 miRNA 在气道上皮纤毛发生中的活性

• 批准号: 9196391
• 负责人: Wellington V. Cardoso
• 金额: $ 41.62万
• 依托单位: COLUMBIA UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-01-01 至 2019-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9196391
• 关键词: Address; Affect; Area; Biological; Bronchitis; Cells; Centrioles; Chronic; Cilia; Complex; Core Protein; Coughing; Cultured Cells; Cytoplasmic Granules; Data; Defect; Development; Disease; Docking; Enzymes; Epithelial Cells; Event; Exonuclease; Gene Silencing; Glycine; Goals; Homeostasis; Human; Impairment; In Vitro; Knowledge; Location; Lung; Lung diseases; Mammalian Cell; Mediating; Messenger RNA; MicroRNAs; Microscopic; Microtubule Polymerization; Molecular Weight; Mucociliary Clearance; Mus; Mutant Strains Mice; Organism; Pathway interactions; Pattern; Phenotype; Play; Poly A; Population; Primary Ciliary Dyskinesias; Process; Proteins; Public Health; Recruitment Activity; Reporting; Respiration Disorders; Role; Scaffolding Protein; Testing; Translations; Trinucleotide Repeats; Tryptophan; Up-Regulation; airway epithelium; base; cell type; cilium biogenesis; derepression; design; genome-wide; in vivo; insight; kinetosome; mutant; novel; primary outcome; programs; public health relevance

 DESCRIPTION (provided by applicant): Tnrc6a proteins are essential for miRNA-mediated gene silencing, a fundamental mechanism required for proper development, homeostasis, and function of an organism. The function and mechanism of Tnrc6a (GW182) and its associated cytoplasmic granules, GW/P-bodies (GWBs) have been well studied in mammalian cells cultured in vitro. However, the significance for the formation of GWBs is unclear. Moreover, the expression, localization and function of Tnrc6a and GWBs during development in vivo are still poorly understood. To study Tnrc6a and GWBs in vivo, we have generated Tnrc6a mutant mice, and shown that Tnrc6a is required for miRNA-induced gene silencing. In this proposal, we will expand our studies to understand a subcellular localized miRNA mechanism that is associated with Tnrc6a and GWBs in multiciliated cells of airways. We have remarkable preliminary observations that Tnrc6a is highly expressed in multiciliated cells and Tnrc6a proteins are concentrated in GWBs that are closely associated with centrioles/basal bodies. Moreover, disruption of Tnrc6a expression leads to major defects in cilia formation. In Aim1, we proposed to determine how Tnrc6a regulates cilia formation and function by affecting key cellular events of ciliogenesis. In Aim 2, we proposed to rigorously characterize these unique multiciliated cell-specific GWBs, and determine the functional significance of formation and localization of Trnc6a/GWBs in ciliogenesis. In Aim3, we will identify the miRNA program associated with these centriole associated GWBs that regulates ciliogenesis. Successful accomplishment of these studies will allow us to identify a novel subcellular localized miRNA mechanism in ciliogenesis that is associated with selectively enriched expression of Tnrc6a and the formation and localization of GWBs. RELEVANCE TO PUBLIC HEALTH: Aberrant expression and function of miRNA activities have been associated with human disorders including primary ciliary dyskinesia (PCD). Studies proposed in this application are aimed to elucidate novel and fundamental miRNA mechanisms that are essential for proper differentiation of multiciliated cells. Results from these studies should provide insight into how miRNAs regulate normal cilia assembly during development and how deregulation of this process leads to defective cilia in human disorders.

 描述（由申请人提供）：Tnrc 6a蛋白是miRNA介导的基因沉默所必需的，这是生物体正常发育、稳态和功能所需的基本机制。Tnrc 6a（GW 182）及其相关的胞质颗粒GW/P体（GWB）在体外培养的哺乳动物细胞中的功能和机制已被充分研究。然而，GWB形成的意义尚不清楚。此外，Tnrc 6a和GWB在体内发育过程中的表达、定位和功能仍然知之甚少。为了在体内研究Tnrc 6a和GWB，我们已经产生了Tnrc 6a突变小鼠，并表明Tnrc 6a是miRNA诱导的基因沉默所必需的。在这个提议中，我们将扩大我们的研究，以了解与气道多纤毛细胞中的Tnrc 6a和GWB相关的亚细胞定位miRNA机制。我们有显着的初步观察，Tnrc 6a是高度表达的多纤毛细胞和Tnrc 6a蛋白集中在GWB是密切相关的中心粒/基体。此外，Tnrc 6a表达的破坏导致纤毛形成的主要缺陷。在Aim 1中，我们提出确定Tnrc 6a如何通过影响纤毛发生的关键细胞事件来调节纤毛的形成和功能。在目标2中，我们提出严格表征这些独特的多纤毛细胞特异性GWB，并确定Trnc 6a/GWB在纤毛发生中的形成和定位的功能意义。在Aim 3中，我们将确定与这些中心粒相关的GWB相关的miRNA程序，这些GWB调节纤毛发生。这些研究的成功完成将使我们能够确定一种新的亚细胞定位的miRNA机制，在纤毛发生，是与选择性富集表达的Tnrc 6a和GWB的形成和定位。与公共卫生的相关性：miRNA活性的异常表达和功能与包括原发性纤毛运动障碍（PCD）在内的人类疾病相关。本申请中提出的研究旨在阐明多纤毛细胞适当分化所必需的新的和基本的miRNA机制。这些研究的结果应该提供深入了解miRNA如何在发育过程中调节正常的纤毛组装，以及该过程的失调如何导致人类疾病中的纤毛缺陷。