Signaling and microRNA function in neurons

神经元中的信号传导和 microRNA 功能

• 批准号: 8189869
• 负责人: DAVID L TURNER
• 金额: $ 23.33万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-01 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8189869
• 关键词: Affect; Animals; Apoptosis; Axon; Binding; Binding Sites; Biochemical; Biological Process; Biology; Cell Death; Cell Survival; Cell physiology; Cells; Cellular Stress; Cellular Stress Response; Chimeric Proteins; Complex; Cytoplasmic Granules; Development; Event; Exhibits; Gene Expression Regulation; Genes; Genetic; Genetic Transcription; Genetic Translation; Health; Homeostasis; Human; Immunoprecipitation; Individual; Intervention; Knowledge; Link; MAP Kinase Gene; MAP-kinase-activated kinase 2; MAPK14 gene; Mediating; Messenger RNA; Methods; MicroRNAs; Mus; Mutation; Nervous system structure; Neuraxis; Neurodegenerative Disorders; Neuronal Differentiation; Neurons; Pathology; Pathway interactions; Phosphorylation; Phosphotransferases; Physiological Processes; Physiology; Play; Population; Post-Transcriptional Regulation; Process; Protein Binding; Proteins; Regulation; Repression; Research; Role; Signal Pathway; Signal Transduction; Site; Tamoxifen; Tissues; Translations; base; crosslink; extracellular; hearing impairment; improved; mRNA Expression; mRNA Stability; mitogen-activated protein kinase p38; nervous system development; nervous system disorder; neurodevelopment; neurogenesis; prevent; response; synaptic function; tumor

DESCRIPTION (provided by applicant): Post-transcriptional regulation of mRNAs by microRNAs is a widespread and essential component of gene regulation in animals. microRNAs, in association with Argonaute (Ago) proteins, bind to specific sequences in mRNAs to repress translation and/or reduce the level of the target mRNAs. Individual microRNAs may regulate many different genes, while individual mRNAs can be targeted by multiple microRNAs. Numerous microRNAs are expressed in the mammalian central nervous system (CNS), and microRNAs have been implicated in the regulation of a variety of processes in the CNS, including neurogenesis, cell survival and death, cell fate determination, neuronal differentiation, axon outgrowth, and synaptic function. Signal transduction plays essential roles in CNS development and function. Intracellular kinase cascades, activated by extracellular signals, directly modulate most biological processes, including transcription and translation. However, it is not known whether repression of target mRNAs by Ago/microRNA complexes can be modulated directly by signaling pathways. Phosphorylation of the Ago-2 protein by the p38 MAP kinase/MAPKAP kinase 2 (MAPKAP-K2) pathway alters its subcellular localization, and p38 kinase/ MAPKAP-K2 signaling is known to regulate mRNA stability and translation, as well as other biological processes. Phosphorylation of the Ago/microRNA complex and associated proteins by p38/MAPKAP-K2 may promote or prevent assembly of repressive complexes on specific mRNAs, leading to the modulation of microRNA-mediated repression on specific subsets of targets in neurons. We propose to use a recently developed method for biochemical purification and high-throughput sequencing of mRNA fragments associated with the Ago-2 protein to identify microRNA target sites at which Ago-2/microRNA binding is modulated by activation or inhibition of the p38 pathway in primary cerebellar granule neurons. We will further characterize selected target mRNAs that exhibit modulated microRNA binding. Modulation of microRNA binding and repression by signaling pathways would significantly expand the scope of biological processes that could be regulated by microRNAs, and may also explain why some predicted microRNA target sites fail to mediate repression. Both microRNAs and the p38 signaling pathway have been implicated in multiple diseases of the nervous system, and p38 plays critical roles during responses to cellular stress and/or apoptosis, physiological processes that are also linked to microRNA functions. Demonstrating that microRNA function can be rapidly modulated in the CNS by signaling, independent of microRNA expression levels, would impact both our understanding of microRNA biology in the nervous system, and of the role of microRNAs and p38 signaling in neurological disease. PUBLIC HEALTH RELEVANCE: Neurological diseases are serious human health problems that affect numerous individuals. The research in this proposal is directed at understanding genetic regulatory mechanisms in nerve cells. The proposed studies will determine whether two distinct mechanisms interact to control genes in nerve cells. This information should contribute to our knowledge of neural development, physiology, and cellular function, as well as our understanding of neurological diseases, and it should help to provide a basis for the development of rational interventions for treating or preventing neurological diseases.

描述(由申请人提供)：microRNAs对mRNAs的转录后调控是动物基因调控中广泛而重要的组成部分。MicroRNAs与ArgAerte(AGO)蛋白结合，与mRNAs中的特定序列结合，抑制翻译和/或降低目标mRNAs的水平。单个的microRNAs可能调控许多不同的基因，而单个的mRNAs可以被多个microRNAs靶向。哺乳动物中枢神经系统(CNS)中表达大量的microRNAs，microRNAs参与调控中枢神经系统的多种过程，包括神经发生、细胞存活和死亡、细胞命运决定、神经元分化、轴突生长和突触功能。信号转导在中枢神经系统的发育和功能中起着至关重要的作用。由细胞外信号激活的细胞内激活级联直接调节大多数生物过程，包括转录和翻译。然而，目前尚不清楚AGO/microRNA复合体对靶mRNAs的抑制是否可以直接通过信号转导途径进行调节。通过p38 MAP/MAPKAP-K2途径使AGO-2蛋白磷酸化，改变其亚细胞定位，p38/MAPKAP-K2信号调节mRNA的稳定性和翻译，以及其他生物学过程。P38/MAPKAP-K2对AGO/microRNA复合体和相关蛋白的磷酸化可能促进或阻止抑制复合体在特定mRNA上的组装，导致microRNA介导的抑制作用在神经元中的特定亚群上的调节。我们建议使用最近发展的一种生化纯化和高通量测序与AGO-2蛋白相关的mRNA片段的方法来确定在初级小脑颗粒神经元中，通过激活或抑制p38通路来调节AGO-2/microRNA结合的microRNA靶点。我们将进一步表征所选的显示调制的microRNA结合的靶mRNAs。通过信号通路调节microRNA的结合和抑制将显著扩大microRNAs可以调节的生物学过程的范围，也可以解释为什么一些预测的microRNA靶点无法介导抑制。MicroRNAs和p38信号通路都与多种神经系统疾病有关，p38在对细胞应激和/或细胞凋亡的反应中发挥关键作用，这些生理过程也与microRNA的功能有关。证明在中枢神经系统中，microRNA的功能可以通过信号快速调节，而与microRNA的表达水平无关，这将影响我们对神经系统中microRNA生物学的理解，以及microRNAs和p38信号在神经系统疾病中的作用。 公共卫生相关性：神经性疾病是严重的人类健康问题，影响着无数人。这项建议中的研究旨在了解神经细胞中的遗传调控机制。这项拟议的研究将确定是否有两种不同的机制相互作用来控制神经细胞中的基因。这些信息应该有助于我们了解神经发育、生理和细胞功能，以及我们对神经疾病的理解，它应该有助于为制定治疗或预防神经疾病的合理干预措施提供基础。