Dissecting the Regulation of Zinc-Homeostasis
Dissecting the Regulation of Zinc-Homeostasis
批准号:
7799763
负责人:
Davin Malasarn
金额:
$5.05万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2011-03-31
关键词:
AlgaeAlzheimer&aposs DiseaseAnimalsBacteriaBiological ModelsBiologyBlast CellCardiacCellsChlamydomonasChlamydomonas reinhardtiiComputer SimulationConsensus SequenceCopperElementsEnsureEnzymesFunctional disorderGene ExpressionGene TargetingGenesGeneticGenetic TranscriptionGenomeGrowthHomeostasisHomologous GeneHumanIronLibrariesLifeLow Birth Weight InfantManganeseMessenger RNAMetabolismMetal Binding SiteMetalloproteinsMetalsMicronutrientsModelingNeuronsNucleic Acid BindingNutrientNutritionalOrganismPathway interactionsPatternPhenotypePhotosynthesisPlantsProcessProteinsReactionReactive Oxygen SpeciesRegulationRegulonReporterRespirationRoleSignal TransductionStagingTailTestingTimeToxic effectTransition ElementsWaterWorkZincZinc deficiencybasechelationcofactorgenetic analysisimmune functioninsightmutantnutritionoperationoxidative damagepublic health relevanceresponsetranscription factor
中文摘要
描述(申请人提供):锌是生命各个领域的生物体所需的300多种已知酶所必需的营养物质。人类缺锌会导致出生体重过低、免疫功能受损、心脏功能障碍和肠病肢端皮炎。过量的锌会干扰其他非锌金属蛋白,并会诱导神经元等细胞的氧化损伤,这可能会导致阿尔茨海默氏症。因此,细胞必须精确地调节锌的动态平衡,以确保它们有足够的锌来允许蛋白质发挥作用,同时将可能造成损害的过量锌的量降至最低。真核藻衣藻为研究锌的稳态调控提供了一个完美的模型系统,因为它可以在广泛的锌浓度下存活,并且含有在动植物中保守的锌反应基因。为了了解衣藻对锌缺乏或毒害的感知和反应,我提出了以下具体目标:1)识别与锌营养的不同阶段有关的基因,并区分转录和转录后机制的运作;2)识别与一个或多个关键的锌反应靶点相关的锌反应元件(ZRE),并评估Crr1在锌稳态中的作用。对衣藻的研究已经为铁和铜的稳态机制提供了有价值的见解,而锌稳态调节的细节将有助于我们更广泛地理解细胞是如何进化到利用金属辅助因子来执行生命的重要功能的。与公共卫生相关:锌是从细菌到人类的各种生物体所需的大量基本营养物质。锌是300多种已知酶所必需的,包括那些参与呼吸、转录和光合作用的酶。在这项工作中,锌感应和适应性反应的机制将被揭开,以了解细胞如何识别和适应锌缺乏和毒性。
英文摘要
DESCRIPTION (provided by applicant): Zinc is an essential nutrient required in over 300 known enzymes by organisms from all domains of life. Zinc deficiency in humans can result in low birth weight, impaired immune function, cardiac dysfunction and acrodermatitus enteropathica. Excess zinc can interrupt other non-zinc metalloproteins and can induce oxidative damage in cells such as neurons, which potentially leads to Alzheimer's Disease. Thus, cells must precisely regulate zinc homeostasis to ensure that they have enough zinc to allow proteins to function while minimizing the amount of excess zinc that can cause damage. The eukaryotic alga Chlamydomonas reinhardtii provides a perfect model system to study the regulation of zinc homeostasis because it can survive under a wide range of zinc-concentrations and contains putative zinc-responsive genes that are conserved in both animals and plants. To understand how Chlamydomonas senses and responds to zinc deficiency or toxicity, I propose the following specific aims: 1) To identify genes that are responsive to distinct stages of zinc nutrition and distinguish the operation of transcriptional vs. post-transcriptional mechanisms, 2) to identify zinc-responsive elements (ZREs) associated with one or more key zinc-responsive targets and assess the role of Crr1, a transcription factor known to regulate both zinc- and copper-responsive genes, in zinc homeostasis and 3) to use a classical genetic approach to identify components of nutritional zinc signal transduction, potentially including regulators and target genes. Studies of Chlamydomonas have already provided valuable insight into the mechanisms of iron and copper homeostasis, and details of zinc-homeostasis regulation will contribute to our broader understanding of how, cells evolved to take advantage of metal cofactors to perform the vital functions of life. Public Health Relevance: Zinc is an essential nutrient required in abundance by organisms ranging from bacteria to humans. Zinc is required by over 300 known enzymes, including those involved in respiration, transcription and photosynthesis. In this work, mechanisms of zinc-sensing and adaptive response will be unraveled to understand how cells recognize and adjust to zinc deficiency and toxicity.
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Dissecting the Regulation of Zinc-Homeostasis
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批准号:7546113
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项目类别:
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资助金额:$4.68万
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财政年份:2009
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负责人:Davin Malasarn
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依托单位: