Systems analysis of mitochondrial genome maintenance in physiological context
Systems analysis of mitochondrial genome maintenance in physiological context
批准号:
10701776
负责人:
Samantha C Lewis
金额:
$38.77万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-09-15 至 2027-08-31
关键词:
ATP Synthesis PathwayAllelesAnimalsBiologyCell physiologyCellsCellular biologyChromosomesComplexDiseaseEukaryotic CellFosteringGenetic TranscriptionGenomeGoalsHealthHeritabilityHomeostasisHumanInvertebratesLiteratureMaintenanceMalignant NeoplasmsMetabolic DiseasesMicroscopyMissionMitochondriaMitochondrial DNAMitochondrial Respiratory Chain DeficienciesModelingMolecularNerve DegenerationOrganellesOxidative PhosphorylationPathway interactionsPhysiologicalProcessProteinsProteomicsRNAResearchSomatic CellSystems AnalysisTissuesUnited States National Institutes of HealthWorkexperimental studyhuman diseaseinsightmitochondrial DNA mutationmitochondrial dysfunctionmitochondrial genomemutantnew therapeutic targetnovelsegregation
中文摘要
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英文摘要
Project Description/Summary
Mitochondrial DNA (mtDNA) encodes RNAs and proteins critical for cell function. However, the
pathways that regulate mtDNA synthesis and segregation in animal cells are not well
understood. The goals of this work are to identify the protein components of mitochondrial DNA
nucleoid complexes, to investigate how mitochondrial replication and dynamics are coordinated
to homeostatically maintain mtDNA nucleoid segregation and abundance, and to probe the
mechanisms underlying selection against mutant mtDNAs in somatic cells. These experiments
will provide fundamental insights into the maintenance of the essential mitochondrial
chromosome in animal cells and how maintenance processes are regulated, potentially leading
to the discovery and characterization of novel pathways that regulate the inheritance of mtDNA
disease alleles. We will employ cutting-edge microscopy of living cells and whole animals,
proteomics, and single cell transcriptional analyses to interrogate the molecular functions of
candidate proteins implicated in the maintenance of mtDNA integrity. These experiments will
reconcile inconsistencies in the mitochondrial biology literature, provide fundamental insight into
the mechanisms of mtDNA copy number control, and identify novel pathways that regulate the
tissue-specific manifestations of mitochondrial dysfunction.
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Systems analysis of mitochondrial genome maintenance in physiological context
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批准号:10898255
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项目类别:
-
资助金额:$8.84万
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财政年份:2022
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负责人:Samantha C Lewis
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依托单位:
Systems analysis of mitochondrial genome maintenance in physiological context
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批准号:10500906
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项目类别:
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资助金额:$37.02万
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财政年份:2022
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负责人:Samantha C Lewis
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依托单位:
Systems analysis of mitochondrial genome maintenance in physiological context
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批准号:10816224
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项目类别:
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资助金额:$1.47万
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财政年份:2022
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负责人:Samantha C Lewis
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依托单位:
Molecular mechanisms of mtDNA inheritance
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批准号:10085799
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项目类别:
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资助金额:$24.9万
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财政年份:2018
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负责人:Samantha C Lewis
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依托单位:
Molecular mechanisms of mtDNA inheritance
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批准号:10371889
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项目类别:
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资助金额:$24.9万
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财政年份:2018
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负责人:Samantha C Lewis
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依托单位:
Systems Analysis of Mammalian Mitochondrial DNA Segregation
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批准号:8831988
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项目类别:
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资助金额:$5.24万
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财政年份:2015
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负责人:Samantha C Lewis
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依托单位:
海外基金