Examining Circadian Changes in Genome Structure
Examining Circadian Changes in Genome Structure
批准号:
8901202
负责人:
WILLIAM J BELDEN
金额:
$27.87万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-05-01 至 2016-07-31
关键词:
Animal ModelBiochemistryBiological ClocksCell NucleusCell physiologyCellsChromatinChromatin StructureCircadian RhythmsCis-Acting SequenceComplexDNADNA MethylationDNA SequenceDataDefectEnsureEnzymesFeedbackFrequenciesGene ExpressionGene FrequencyGenesGeneticGenetic TranscriptionGenomeGlobal ChangeHealthHeterochromatinHistone H3HistonesHumanIndiumLysineMass Spectrum AnalysisMetabolismMethylationMethyltransferaseModificationMolecularNeurosporaNormal CellNucleosomesOrganismOutputPathway interactionsPhasePlayPositioning AttributeProcessProteinsRegulationResearchRoleRunningStructureSystemTechnologyTimeTranscriptTranscription CoactivatorUntranslated RNAchromatin modificationchromatin remodelingcircadian pacemakerdesigngenome-widehistone modificationinnovationinsightinterestmethod developmentmutantprogramspromoterresearch study
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Research over the past decade has revealed an important role for chromatin-modifying and chromatin-remodeling enzymes in coordinated regulation of the circadian clock. This is not unexpected given that a core element in eukaryotic circadian clocks is a transcriptional negative feedback loop. Chromatin functions to organize eukaryotic DNA, but also creates a barrier for transcription. This necessitates a role for chromatin remodeling in maintaining circadian rhythms. In this proposal, I am seeking to further define the modifications that occur at the Neurospora central clock gene frequency and examine the role of heterochromatin in clock and clock-controlled gene expression. Experiments discussed herein will examine this problem using a combined approach. In Specific Aim 1, I propose to isolate the central clock gene frequency in its native chromatin state and identify chromatin modification by Mass Spectrometry. In Specific Aim 2, I will examine how the KMT1 DIM-5 is directed to chromatin and the role of H3K9 methylation in clock and clock controlled gene expression. In Specific Aim 3, I examine if there are circadian clock-regulated changes to genome structure. Data obtained in these aims will be compared and contrasted to understand the relationship between genome structure and clock regulated gene expression. Overall, this proposal will further our understanding of how chromatin structural changes effects circadian regulated gene expression.
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会议论文
Administrative Supplement to Recover Losses for the Project entitled "Examining C
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批准号:8679554
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项目类别:
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资助金额:$13.04万
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财政年份:2013
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负责人:WILLIAM J BELDEN
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依托单位:
Examining Circadian Changes in Genome Structure
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批准号:8276721
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项目类别:
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资助金额:$27.18万
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财政年份:2012
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负责人:WILLIAM J BELDEN
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依托单位:
Examining Circadian Changes in Genome Structure
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批准号:8610328
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项目类别:
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资助金额:$27.9万
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财政年份:2012
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负责人:WILLIAM J BELDEN
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依托单位:
Examining Circadian Changes in Genome Structure
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批准号:8459989
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项目类别:
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资助金额:$27.4万
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财政年份:2012
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负责人:WILLIAM J BELDEN
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依托单位:
Role of Chromatin Remodeling in Circadian Regulation
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批准号:6792425
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项目类别:
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资助金额:$4.73万
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财政年份:2004
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负责人:WILLIAM J BELDEN
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依托单位:
Role of Chromatin Remodeling in Circadian Regulation
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批准号:6895893
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项目类别:
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资助金额:$4.99万
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财政年份:2004
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负责人:WILLIAM J BELDEN
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依托单位:
Role of Chromatin Remodeling in Circadian Regulation
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批准号:7067122
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项目类别:
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资助金额:$5.2万
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财政年份:2004
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负责人:WILLIAM J BELDEN
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依托单位:
海外基金