Regulation of Retinal Physiology by micro-RNAs

micro-RNA 对视网膜生理学的调节

基本信息

批准号：
8431587
负责人：
Krzysztof Palczewski
金额：
$ 35.55万
依托单位：
CASE WESTERN RESERVE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2013
资助国家：
美国
起止时间：
2013-03-01 至 2018-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8431587
关键词：
Adult Algorithms Anatomy Animals Base Pairing Biochemical Bioinformatics Cell Death Cells Cessation of life Data Degenerative Disorder Development Disease Disease model Event Exhibits Exposure to Eye Gene Cluster Gene Expression Gene Expression Profile Gene Expression Regulation Gene Targeting Genes Health Immunoprecipitation Investigation Knockout Mice Light Link Measures Mediating Messenger RNA MicroRNAs Mitotic Molecular Mus Open Reading Frames Organ Pathology Pathway interactions Phenotype Photoreceptors Physiological Physiological Processes Physiology Plants Play Porifera Protein Biosynthesis Proteins RNA RNA Binding RNA-Binding Proteins RNA-Induced Silencing Complex Regulation Repression Residual state Retina Retinal Retinal Degeneration Retinitis Pigmentosa Role Seeds Sensory Site Stress Techniques Technology Tissues Translational Repression Translations Visual system structure base crosslink in vivo insight interest loss of function mouse model new technology next generation sequencing novel novel strategies paralogous gene prevent public health relevance research study treatment strategy vision development

项目摘要

DESCRIPTION (provided by applicant): Micro-RNAs (miRNAs) are small, stable RNA molecules that post-transcriptionally regulate gene expression in plants and animals. They act by base pairing to partially complementary sequences on target messenger RNAs to inhibit protein synthesis, primarily through translational repression and mRNA destabilization. More than 250 miRNAs are reportedly expressed in the retina, and miRNA gene regulation has been shown to impact retinal development, function, and disease. miRs -96, -183, and -182 comprise an evolutionarily conserved, paralogous gene cluster. Simultaneous partial disruption of the activities of these miRNAs in photoreceptors results in a robust light-induced retinal degeneration phenotype, implying that these miRNAs serve a neuroprotective function during exposure to light. Thus, this miRNA-mediated photoreceptor survival pathway is a novel target for potential therapy of retinal degenerative disorders. To evaluate the impact of the miR-183 cluster on photoreceptor survival more directly in the context of retinal degenerative disease, the consequences of miR-183 cluster loss-of-function will be evaluated in new mouse models of autosomal dominant and autosomal recessive retinitis pigmentosa. A knockout mouse model will be generated to determine the impact of complete loss of miRNA cluster activity. Additionally, a combination of 'top-down' and 'bottom-up' approaches will be employed to dissect out the molecular events underlying miRNA-mediated photoreceptor protection. Newly developed biochemical techniques will be used to identify functionally relevant direct targets of these miRNAs in the retina, and next generation sequencing technology will be employed to evaluate miRNA cluster-dependent alterations in gene expression that occur after exposure to intense light. Results of these investigations will provide insights into gene regulation networks involved in protecting photoreceptors against stress-induced death. These experiments promise to yield novel approaches to treat or prevent blinding diseases.

描述（由申请人提供）：Micro-RNA (miRNA) 是小而稳定的 RNA 分子，可在植物和动物中转录后调节基因表达。它们通过与目标信使 RNA 上的部分互补序列碱基配对来抑制蛋白质合成，主要是通过翻译抑制和 mRNA 不稳定。据报道，超过 250 个 miRNA 在视网膜中表达，并且 miRNA 基因调控已被证明会影响视网膜的发育、功能和疾病。 miR -96、-183和-182包含进化上保守的旁系同源基因簇。同时部分破坏光感受器中这些 miRNA 的活性会导致强烈的光诱导视网膜变性表型，这意味着这些 miRNA 在暴露于光期间具有神经保护功能。因此，这种 miRNA 介导的光感受器存活途径是视网膜退行性疾病潜在治疗的新靶点。为了在视网膜退行性疾病的背景下更直接地评估 miR-183 簇对光感受器存活的影响， miR-183簇功能丧失的后果将在常染色体显性和常染色体隐性视网膜色素变性的新小鼠模型中进行评估。将生成基因敲除小鼠模型以确定 miRNA 簇活性完全丧失的影响。此外，“自上而下”和“自下而上”方法的结合将被用来剖析 miRNA 介导的光感受器保护的分子事件。新开发的生化技术将用于识别这些 miRNA 在视网膜中功能相关的直接靶标，下一代测序技术将用于评估暴露于强光后发生的 miRNA 簇依赖性基因表达变化。这些研究的结果将提供对保护光感受器免受压力诱导死亡的基因调控网络的见解。这些实验有望产生治疗或预防致盲疾病的新方法。