Metal Homeostasis in Yeast
Metal Homeostasis in Yeast
批准号:
7893075
负责人:
Dennis J Thiele
金额:
$33.59万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-04-01 至 2013-06-30
关键词:
AffectAnabolismAnemiaBinding ProteinsBiochemicalBiotinCell Cycle ProgressionCell ProliferationCellsChildCitric Acid CycleDNA biosynthesisDefectElementsEnzymesEukaryotic CellFatigueFatty AcidsGenesGrowth and Development functionHealthHemeHomeostasisHumanInvestigationIronLifeLightLinkMalnutritionMessenger RNAMetabolicMetabolismMetalsMitochondriaMolecularMotorOrganismOxidation-ReductionOxidative PhosphorylationPerformance at workPhotosynthesisPhysiologicalPhysiological ProcessesProteinsRegulationSeveritiesSourceSupplementationWomen&aposs HealthYeastsaminoacid biosynthesiscell growthchromatin modificationcognitive functioncopingimmune functionlipid metabolismmRNA StabilitymRNA Transcript Degradationoxygen transportprotein functionpublic health relevancerepairedresearch studyresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Summary Iron (Fe) is an essential element that serves as a biochemical co-factor for a wide variety of enzymes and proteins that function in oxygen transport, mitochondrial oxidative phosphorylation, DNA replication and repair, intermediary metabolism, lipid metabolism, chromatin modification and a host of other critical physiological processes. Fe deficiency is the most common nutritional deficiency on earth, with health consequences that include anemia, delayed growth and development, abnormal motor and cognitive function, decreased immune function, thermoreguatory defects, fatigue and decreased work performance. While Fe deficiency leads to severe health consequences, the detailed molecular mechanisms that allow graded responses to a range of severity of Fe deficiency are not well understood. This proposal describes avenues of investigation to understand fundamental mechanisms whereby eukaryotic cells respond and adapt to Fe deficiency. The first specific aim outlines experiments to decipher the mechanisms by which the yeast Cth1 and Cth2 proteins differentially target mRNAs for degradation in response to Fe deficiency, leading to cellular metabolic adaptation to allow cells to cope with reduced Fe availability. The second specific aim describes experiments to understand how expression of the Cth1 and Cth2 proteins is exquisitely fine-tuned in response to Fe deficiency, the physiological importance of this regulation with respect to Fe homeostasis and its potential link to changes in cell cycle progression. Given the common occurrence of Fe deficiency and its disproportionate affects on the health of women and children, the studies outlined in this application will provide fundamentally important information on the mechanisms by which cells homeostatically respond to Fe deficiency. PUBLIC HEALTH RELEVANCE: Fe deficiency is the most common nutritional deficiency on earth, with health consequences that include anemia, delayed growth and development, abnormal motor and cognitive function, decreased immune function, thermoregulatory defects, fatigue and decreased work performance. Given the common occurrence of Fe deficiency and its disproportionate affects on the health of women and children, the studies outlined in this application will provide fundamentally important information on the mechanisms by which cells adapt to Fe deficiency.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
2015 Cell Biology of Metals Gordon Research Conference
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批准号:8974528
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项目类别:
-
资助金额:$2.52万
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财政年份:2015
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负责人:Dennis J Thiele
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依托单位:
Mechanism for copper-deficiency mediated neutropenia
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批准号:8605173
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项目类别:
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资助金额:$23.55万
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财政年份:2013
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负责人:Dennis J Thiele
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依托单位:
Mechanism for copper-deficiency mediated neutropenia
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批准号:8504553
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项目类别:
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资助金额:$19.63万
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财政年份:2013
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负责人:Dennis J Thiele
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依托单位:
HSF1 as a therapeutic target in neurodegenerative disease
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批准号:8423028
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项目类别:
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资助金额:$31.83万
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财政年份:2010
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负责人:Dennis J Thiele
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依托单位:
HSF1 as a therapeutic target in neurodegenerative disease
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批准号:8220871
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项目类别:
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资助金额:$33.0万
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财政年份:2010
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负责人:Dennis J Thiele
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依托单位:
HSF1 as a therapeutic target in neurodegenerative disease
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批准号:8019461
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项目类别:
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资助金额:$33.01万
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财政年份:2010
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负责人:Dennis J Thiele
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依托单位:
HSF1 as a therapeutic target in neurodegenerative disease
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批准号:7882166
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项目类别:
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资助金额:$33.69万
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财政年份:2010
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负责人:Dennis J Thiele
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依托单位:
FASEB Summer Research Conference "Trace Element Metabolism: Basic and Applied Res
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批准号:7484010
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项目类别:
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资助金额:$1.2万
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财政年份:2008
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:9317601
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项目类别:
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资助金额:$43.48万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:8300126
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项目类别:
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资助金额:$33.71万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:7367133
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项目类别:
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资助金额:$25.98万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:8519990
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项目类别:
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资助金额:$32.52万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:8187063
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项目类别:
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资助金额:$38.77万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:7565996
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项目类别:
-
资助金额:$25.98万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:8895305
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项目类别:
-
资助金额:$33.67万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Mammals
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批准号:8708039
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项目类别:
-
资助金额:$33.69万
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财政年份:2001
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负责人:Dennis J Thiele
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依托单位:
Copper Homeostasis in Yeast
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批准号:7326809
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项目类别:
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资助金额:$31.83万
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财政年份:1989
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负责人:Dennis J Thiele
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依托单位:
Metal Homeostasis in Yeast
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批准号:8294642
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项目类别:
-
资助金额:$33.25万
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财政年份:1989
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负责人:Dennis J Thiele
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依托单位:
Metal Homeostasis in Yeast
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批准号:7729386
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项目类别:
-
资助金额:$33.93万
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财政年份:1989
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负责人:Dennis J Thiele
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依托单位:
Metal Homeostasis in Yeast
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批准号:8094263
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项目类别:
-
资助金额:$33.25万
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财政年份:1989
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负责人:Dennis J Thiele
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依托单位:
海外基金