Extremely high-throughput mapping of protein, RNA, and chromatin interactions in health and disease
Extremely high-throughput mapping of protein, RNA, and chromatin interactions in health and disease
批准号:
10453756
负责人:
Sheng Zhong
金额:
$74.79万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-07-30 至 2025-06-30
关键词:
BindingBlood VesselsCellsChromatinChronicCompanionsDNADiabetes MellitusDiseaseEndocrinologyEndothelial CellsGene ExpressionGenomicsHealthHyperglycemiaInflammationMapsMetabolic DiseasesMolecularProteinsRNAResearchRoleSystemTechnologyTimeVascular Endothelial Cellbioinformatics toolcatalystcell typediabetic ulcerdiabetic wound healingendothelial dysfunctiongenome-widehigh throughput technologywhole genome
中文摘要
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英文摘要
Extremely high-throughput mapping of protein, RNA, and chromatin interactions in health and disease
Abstract
This Catalyst project aims to removing a major bottleneck in understanding diabetes and its complications, by
developing the technologies to map diverse molecular interactions in the disease-relevant cells at the genomic
scale. These proposed technologies, collectively called PRACI (Protein, RNA, and chromatin interactions), will
enable a typical research lab to map genome-wide protein-protein, RNA-protein, RNA-RNA, and RNA-
DNA/chromatin interaction networks from a given cell type within 1 months’ time. PRACI enables typical labs to
compare molecular interaction networks between health and disease states. Without PRACI, genome-wide
mapping of even a single type of interactions from a disease-relevant cell type remains a formidable task.
I will systematically map molecular interactome changes related to diabetes related vascular complications, using
hyperglycemia and chronic inflammation-induced irreversible alterations vascular endothelial cells as a testbed
system. I anticipate to reveal which components of the multiscale molecular networks are responsible for the
sustained dysregulation of gene expression in dysfunctional endothelial cells. Such information will lead to new
perspectives to diabetic wound healing, given the established roles of endothelial dysfunction to diabetic wounds
and the relative accessibility of vasculature. I anticipate that these technologies and their enabled discoveries
will contribute to and inspire transformative changes in the study of Diabetes, Endocrinology, and Metabolic
Diseases.
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Extremely high-throughput mapping of protein, RNA, and chromatin interactions in health and disease
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批准号:10226341
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资助金额:$77.01万
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Extremely high-throughput mapping of protein, RNA, and chromatin interactions in health and disease
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财政年份:2015
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依托单位:
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批准号:9137717
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资助金额:$77.11万
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财政年份:2015
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负责人:Sheng Zhong
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依托单位:
The second phase of NIH Common Fund 4D Nucleome Network Organizational Hub
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批准号:10263369
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项目类别:
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资助金额:$142.76万
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财政年份:2015
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依托单位:
Mapping RNA interactomes by sequencing
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批准号:8948433
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项目类别:
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资助金额:$77.5万
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财政年份:2015
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依托单位:
The second phase of NIH Common Fund 4D Nucleome Network Organizational Hub
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资助金额:$150.0万
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Evolutionary models for gene regulatory networks
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批准号:8786708
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资助金额:$197.07万
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财政年份:2010
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负责人:Sheng Zhong
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依托单位:
Evolutionary models for gene regulatory networks
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批准号:7981841
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资助金额:$36.23万
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财政年份:2010
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依托单位:
DNA methylation in the development of pediatric leukemias
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资助金额:$7.73万
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财政年份:2009
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依托单位:
DNA methylation in the development of pediatric leukemias
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资助金额:$7.73万
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财政年份:2009
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依托单位:
海外基金