mRNA Localization in Organelle Biogenesis
mRNA Localization in Organelle Biogenesis
批准号:
8705543
负责人:
Christopher V. Nicchitta
金额:
$30.57万
依托单位:
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:
2012-09-30 至 2016-07-31
关键词:
3&apos Untranslated Regions5&apos Untranslated RegionsAgeBindingBiochemicalBiogenesisCell LineCell SurvivalCellsCellular biologyChargeCytoplasmCytosolDataDetergentsDiseaseEndoplasmic ReticulumEukaryotic CellEventFoundationsFractionationFunctional disorderGene Expression ProfileGenomeGoalsGolgi ApparatusHydrophobicityIn Situ HybridizationIndividualInheritedIntegral Membrane ProteinInterphaseLengthMaintenanceMediatingMembraneMembrane Protein TrafficMetabolic DiseasesMitoticModelingMolecularOpen Reading FramesOrganellesPathway interactionsPatternPeptide Signal SequencesProtein BiosynthesisProteinsProteomicsRNARNA-Binding ProteinsRegulationReporter GenesReportingResearchResistanceRibosomesRoleSignal Recognition ParticleSignal TransductionSiteSurveysSystemTestingTranslationsbasecohortcombinatorialgenome wide association studygenome-wideinsightmutantprotein transportreceptorrepairedself organizationstable cell linetherapeutic developmenttranscriptome sequencing
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Understanding the molecular principles that regulate endomembrane organelle maintenance and biogenesis stands as a principle question in cell biology. Research to date has established the protein/membrane trafficking pathways that support endomembrane organelle maintenance and through these studies, the central importance of the ER as the site of resident endomembrane protein synthesis has been identified. The molecular basis for endomembrane organelle biogenesis remains, however, mysterious. The objective of the proposed research is to define the role of ER-directed mRNA localization in endomembrane organelle biogenesis. It is well established that the protein trafficking pathways of eukaryotic cells also direct the partitioning of the mRNA transcriptome between the two primary protein synthesis compartments in the cell, the cytoplasm and the endoplasmic reticulum (ER). Thus, mRNAs encoding secretory/integral membrane proteins are localized to the ER via the Signal Recognition Particle (SRP) pathway and mRNAs encoding cytosolic/nucleoplasmic proteins, which lack encoded signal sequences, retain default localization in the cytosol. Although this positive selection model is well established, we have recently reported that i) mRNAs encoding resident proteins of the endomembrane organelles (mRNAendo) can be localized to the ER via a SRP- and translation-independent pathway; ii) the mRNAendo cohort is bound to the ER via direct, ribosome-independent interactions; and iii) the mRNAendo cohort is distinguished by its exceptionally high ER enrichment. These findings suggest that mRNA localization serves an integral, though unexplored, role in organelle biogenesis. We hypothesize that the autonomous localization of endomembrane resident protein-encoding mRNAs to the ER, and their direct, ribosome-independent association with the ER membrane, represents a self-organization mechanism functioning in organelle biogenesis. This hypothesis will be tested in the following specific aims: 1) Establish, at a genome-wide scale, the subcellular partitioning patterns of endomembrane resident protein-encoding mRNAs; 2) Identify the molecular signals that direct endomembrane resident protein-encoding mRNAs to the ER; 3) Identify the RNA binding proteins and ER resident proteins that mediate ribosome-independent association of mRNAs with the ER membrane; 4) Determine if ribosome-independent binding of endomembrane protein encoding mRNAs to the ER is essential for organelle biogenesis. Genome-wide studies of mRNA partitioning in eukaryotic cells have revealed an unexpected complexity in the subcellular patterns of mRNA localization. In this proposal, we propose to extend recent discoveries of mRNA cohort-specific patterns of RNA localization to the ER to the question of organelle biogenesis. If successful, these studies will provide fundamental insights into the molecular principles of organelle biogenesis and support the development of therapeutic approaches to diseases of organelle dysfunction.
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会议论文
Mechanisms of RNA localization and translational regulation on the endoplasmic reticulum
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批准号:10460908
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项目类别:
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资助金额:$64.66万
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财政年份:2021
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanisms of RNA localization and translational regulation on the endoplasmic reticulum
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批准号:10667577
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项目类别:
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资助金额:$64.66万
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财政年份:2021
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负责人:Christopher V. Nicchitta
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依托单位:
mRNA Localization in Organelle Biogenesis
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批准号:8546424
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项目类别:
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资助金额:$29.52万
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财政年份:2012
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负责人:Christopher V. Nicchitta
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依托单位:
mRNA Localization in Organelle Biogenesis
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批准号:8928004
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项目类别:
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资助金额:$30.54万
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财政年份:2012
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanisms of mRNA Anchoring and Translation Regulation on the Endoplasmic Reticulum
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批准号:9310300
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项目类别:
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资助金额:$30.72万
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财政年份:2012
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanisms of mRNA Anchoring and Translation Regulation on the Endoplasmic Reticulum
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批准号:9752327
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项目类别:
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资助金额:$30.68万
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财政年份:2012
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负责人:Christopher V. Nicchitta
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依托单位:
mRNA Localization in Organelle Biogenesis
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批准号:8287757
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项目类别:
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资助金额:$30.62万
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财政年份:2012
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负责人:Christopher V. Nicchitta
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依托单位:
Regulation of mRNA Partitioning to the Endoplasmic Reticulum
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批准号:7925401
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项目类别:
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资助金额:$34.32万
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财政年份:2009
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负责人:Christopher V. Nicchitta
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依托单位:
Regulation of mRNA Partitioning to the Endoplasmic Reticulum
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批准号:7616757
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项目类别:
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资助金额:$29.64万
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财政年份:2007
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负责人:Christopher V. Nicchitta
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依托单位:
Regulation of mRNA Partitioning to the Endoplasmic Reticulum
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批准号:7841846
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项目类别:
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资助金额:$29.34万
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财政年份:2007
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负责人:Christopher V. Nicchitta
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依托单位:
Regulation of mRNA Partitioning to the Endoplasmic Reticulum
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批准号:7413408
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项目类别:
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资助金额:$29.64万
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财政年份:2007
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负责人:Christopher V. Nicchitta
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依托单位:
Regulation of mRNA Partitioning to the Endoplasmic Reticulum
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批准号:7258994
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项目类别:
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资助金额:$28.77万
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财政年份:2007
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanism of Chaperone-Mediated Tumor Rejection
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批准号:6868835
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项目类别:
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资助金额:$25.26万
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财政年份:2004
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanism of Chaperone-Mediated Tumor Rejection
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批准号:7342061
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项目类别:
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资助金额:$23.95万
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财政年份:2004
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanism of Chaperone-Mediated Tumor Rejection
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批准号:6710221
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项目类别:
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资助金额:$25.26万
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财政年份:2004
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanism of Chaperone-Mediated Tumor Rejection
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批准号:7026918
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项目类别:
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资助金额:$24.66万
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财政年份:2004
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负责人:Christopher V. Nicchitta
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依托单位:
Mechanism of Chaperone-Mediated Tumor Rejection
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批准号:7214632
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项目类别:
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资助金额:$23.95万
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财政年份:2004
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负责人:Christopher V. Nicchitta
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依托单位:
MOLECULAR MECHANISM OF GRP94 FUNCTION
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批准号:2388867
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项目类别:
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资助金额:$21.95万
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财政年份:1997
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负责人:Christopher V. Nicchitta
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依托单位:
MOLECULAR MECHANISM OF GRP94 FUNCTION
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批准号:2749636
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项目类别:
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资助金额:$20.77万
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财政年份:1997
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负责人:Christopher V. Nicchitta
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依托单位:
The Molecular Mechanism of GRP94 Function
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批准号:6875771
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项目类别:
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资助金额:$23.87万
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财政年份:1997
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负责人:Christopher V. Nicchitta
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依托单位:
海外基金