Systems-wide analysis of oxidative stress-responsive m6A epitranscriptome
Systems-wide analysis of oxidative stress-responsive m6A epitranscriptome
批准号:
10190951
负责人:
Yi-Lan Weng
金额:
$40.23万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-06-15 至 2025-03-31
关键词:
3&apos Untranslated RegionsAddressAxonBiological MarkersBiological ProcessCatalytic DomainCellsCharacteristicsComplexDataDependenceDevelopmentDiagnosticDiseaseEmbryoEnvironmental ExposureEtiologyExposure toHealthHela CellsHumanInvestigationKidneyLengthLinkLiteratureMass Spectrum AnalysisMediatingMental disordersMetabolismMethodologyMethodsMethylationMethyltransferaseModificationMolecularNervous System controlNeurodegenerative DisordersNeuronsOxidative StressPathogenesisPathogenicityPathologicPathway interactionsPatternPhysiologicalPlayPredispositionPrevention strategyProcessProtein IsoformsRNARNA TransportRegulationRegulatory ElementResearchRiskRoleSignaling MoleculeSpecific qualifier valueStimulusStressSynapsesSystemTo specifyToxic Environmental SubstancesToxicant exposureTranscriptValidationWorkadverse outcomebasebiological adaptation to stressbiomarker identificationdesigndisorder riskepitranscriptomeepitranscriptomicsgene environment interactiongenome-widehuman diseaseinnovationinsightinterestmethylation patternnervous system disordernovelprotein TDP-43responsesodium arsenitetoxicanttranscriptometreatment strategy
中文摘要
项目摘要/摘要
最近表位转录组学领域的出现为理解和操纵提供了可能
生物过程中涉及的一个以前被低估的监管层。特别是,我们的研究
重点关注m6A作为一个感兴趣的候选,因为它是神经中最流行的RNA修饰
控制RNA代谢的多个方面的系统。我们之前已经展示了M6A的关键作用
轴突可塑性和突触活动的调节。这一建议扩大了我们的研究范围,并将重点放在
M6A表位转录组如何使用创新的方法对环境扰动做出反应
识别与不良结果相关的生物标记物和分子途径。我们将在系统范围内使用
解决以下问题的方法:(一)重塑m6A表位转录组的机制是什么
在毒物暴露后,(Ii)m6A的动态如何重塑转录组?(Iii)什么是
与疾病状态和风险相关的错误定位的RNA的特征?我们希望我们的
拟议的研究将显著提高我们对表位转录调控过程的理解
构成环境挑战后的关键致病机制。从我们的系统中获得的数据
简档分析和功能验证可以为开发诊断和/或生物标志物提供新的机会
促进为这些疾病制定更有效的预防和治疗战略。
英文摘要
PROJECT SUMMARY/ABSTRACT
The recent emergence of the epitranscriptomics field has opened the possibility to understand and manipulate
a previously underappreciated regulatory layer involved in biological processes. In particular, our research
focuses on m6A as a candidate of interest given that it is the most prevalent RNA modification in the nervous
system that controls multiple aspects of RNA metabolism. We have previously shown the critical roles of m6A
regulation in axonal plasticity and synaptic activity. This proposal extends our research scope and focuses on
how the m6A epitranscriptome responds to environmental perturbation using innovative methods for the
identification of biomarkers and molecular pathways linked to adverse outcomes. We will use system-wide
approaches to address the following questions: (i) What is the mechanism to remodel the m6A epitranscriptome
upon toxicant exposure, (ii) How do the dynamics of m6A reshape the transcriptome? (iii) What are the
characteristics of mis-localized RNA that are associated with disease state and risk? We expect that our
proposed study will significantly advance our understanding of how epitranscriptomic regulatory processes
constitute key pathogenic mechanisms following environmental challenges. Data gained from our systematic
profiling and functional validation may offer new opportunities for developing diagnostics and/or biomarkers to
facilitate the development of more effective prevention and treatment strategies for these diseases.
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Systems-wide analysis of oxidative stress-responsive m6A epitranscriptome
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批准号:10375555
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项目类别:
-
资助金额:$40.23万
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财政年份:2020
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负责人:Yi-Lan Weng
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依托单位:
海外基金