A Community Zebrafish Resource for Modeling GWAS Biology
A Community Zebrafish Resource for Modeling GWAS Biology
批准号:
10225566
负责人:
Wolfram Goessling
金额:
$77.09万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-05-01 至 2023-07-31
关键词:
ATAC-seqAffectAlgorithm DesignAllelesAnimal ModelArchivesAwardBioinformaticsBiologicalBiological AssayBiological ModelsBiologyBloodCRISPR/Cas technologyCandidate Disease GeneCatalogsCell LineageChIP-seqCodeCommunitiesCompanionsComplementComplexDNA methylation profilingDatabasesDevelopmentDiseaseDisease modelEpigenetic ProcessEtiologyEvaluationFishesGene ExpressionGenesGeneticGenetic ModelsGenetic VariationGenomic SegmentGenomicsGuide RNAHeartHumanHuman BiologyHuman GeneticsHuman GenomeIndividualLiverLocationMaintenanceMapsMedicalModelingMolecularMosaicismNucleic Acid Regulatory SequencesOrganPathway interactionsPharmaceutical PreparationsPhenotypeProductionReagentRegulator GenesRegulatory ElementResearch PersonnelResourcesRoleSignal TransductionStudy modelsSurveysSystemTechnologyTestingTissuesTransgenic OrganismsTranslationsUntranslated RNAVariantWhole OrganismWorkZebrafishalgorithmic methodologiesassay developmentbasecell typedisease mechanisms studydisease phenotypedrug discoveryexperiencegain of functiongene functiongene interactiongenetic variantgenome editinggenome wide association studygenomic locusgenomic variationhuman diseasein vivoin vivo Modelinnovationinsightmouse geneticsmutantnovelnovel strategiesresponsesearchable databasetraittranscriptome sequencingweb site
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY:
Our proposal “Community Zebrafish Resource for Modeling GWAS Biology” applies novel approaches,
algorithms and methods developed within our consortium for functional analysis of human GWAS hits using
the zebrafish model system. Our consortium has accumulated broad experience in zebrafish genetics, genome
editing, bioinformatics, functional assay development, and human disease modeling as well as innovative
mechanistic studies to elucidate individual gene function. During the previous cycle of the award, we
established efficient high-content platforms for the functional analysis of coding sequence variation in zebrafish
to complement GWAS projects across a variety of complex human traits, and provided pathway entry points
and genetic models for understanding disease. In this renewal application, we extend our functional exploration
of single and/or multiple GWAS loci and their roles in biological networks underlying human medical traits to
include prevalent non-coding variation and drug responses through the following Specific Aims:
Aim 1-Functionally analyze loci from multiple GWAS studies on blood, liver, heart and vessel traits, optimizing
assay development and gene editing using CRISPR-Cas9 technology in zebrafish.
a) Using validated assays we will examine the function of multiple coding genes in GWAS loci and
generate genetic models in the zebrafish using CRISPR-Cas9 technology.
b) Accelerate in vivo gene function evaluation by optimization of genome editing in zebrafish using the
CRISPR-Cas9 technology.
Aim 2-Survey landscapes of genomic regulatory regions in different cell lineages in zebrafish and use the
information to support better mapping and functional evaluation of regulatory variants from GWAS loci.
a) Using ATAC-seq, ChIP-seq, Methyl-seq, and companion RNA-seq analyses we will establish a
comprehensive database of conserved (orthologous) regulatory regions in different cell lineages and organs of
both zebrafish and human. We will define regulatory regions in different cell types at different developmental
stages which are important for cell lineage differentiation, maintenance and function in zebrafish.
b) We will map regulatory effects from GWAS loci to conserved zebrafish regulatory regions and test
individual and/or multiple regulatory effects for their roles in specific GWAS traits using genome editing
technology and validated functional assays in zebrafish.
c) Categorize conserved GWAS loci based on function and catalog genome editing reagents for
disease modeling and mechanistic studies and drug discovery.
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The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction.
MAPRE2 和微管在维持正常心室传导中的作用。
DOI:
10.1161/circresaha.123.323231
发表时间:
2024
期刊:
Circulation research
影响因子:
20.1
作者:
[Chiang,DavidY, Verkerk,ArieO, Victorio,Rachelle, Shneyer,BorisI, vanderVaart,Babet, Jouni,Mariam, Narendran,Nakul, Kc,Ashmita, Sampognaro,JamesR, Vetrano-Olsen,Franki, Oh,JohnS, Buys,Eva, deJonge,Berend, Shah,DisheetA, Kiviniemi,Tu]
通讯作者:
Kiviniemi,Tu
DOI:
10.1242/dmm.011726
发表时间:
2013-09
期刊:
Disease models & mechanisms
影响因子:
4.3
作者:
[Liu LY, Fox CS, North TE, Goessling W]
通讯作者:
Goessling W
DOI:
10.1172/jci.insight.163929
发表时间:
2023-01-10
期刊:
JCI INSIGHT
影响因子:
8
作者:
[Oderberg, Isaac M., Goessling, Wolfram]
通讯作者:
Goessling, Wolfram
DOI:
10.3791/62349
发表时间:
2021-04-04
期刊:
Journal of visualized experiments : JoVE
影响因子:
--
作者:
[Oderberg IM, Goessling W]
通讯作者:
Goessling W
DOI:
10.1038/ncomms12061
发表时间:
2016-07-08
期刊:
Nature communications
影响因子:
16.6
作者:
[Wang M, Sips P, Khin E, Rotival M, Sun X, Ahmed R, Widjaja AA, Schafer S, Yusoff P, Choksi PK, Ko NS, Singh MK, Epstein D, Guan Y, Houštěk J, Mracek T, Nuskova H, Mikell B, Tan J, Pesce F, Kolar F, Bottolo L, Mancini M, Hubner N, Pravenec M, Petretto E, MacRae C, Cook SA]
通讯作者:
Cook SA
共 18 条
The Role of Macrophages in Hepatobiliary Development
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批准号:10680846
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资助金额:$61.6万
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财政年份:2023
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负责人:Wolfram Goessling
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依托单位:
A community resource for germline and somatic genetic disease modeling in zebrafish
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批准号:10723158
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资助金额:$89.62万
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财政年份:2023
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The role of liver progenitor cells in liver regeneration
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批准号:10607301
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项目类别:
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资助金额:$66.91万
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财政年份:2023
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负责人:Wolfram Goessling
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依托单位:
Metabolic Regulation of Liver Growth
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批准号:9975140
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项目类别:
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资助金额:$54.71万
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财政年份:2016
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负责人:Wolfram Goessling
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依托单位:
Metabolic Regulation of Liver Growth
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批准号:9765300
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项目类别:
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资助金额:$54.71万
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财政年份:2016
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负责人:Wolfram Goessling
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依托单位:
Metabolic Regulation of Liver Growth
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批准号:9315803
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项目类别:
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资助金额:$54.71万
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财政年份:2016
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负责人:Wolfram Goessling
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依托单位:
A Community Zebrafish Resource for Modeling GWAS Biology
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批准号:8840336
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项目类别:
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资助金额:$81.07万
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财政年份:2014
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负责人:Wolfram Goessling
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A Community Zebrafish Resource for Modeling GWAS Biology
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批准号:8609133
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项目类别:
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资助金额:$85.03万
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财政年份:2014
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负责人:Wolfram Goessling
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依托单位:
A Community Zebrafish Resource for Modeling GWAS Biology
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批准号:9763679
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项目类别:
-
资助金额:$77.09万
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财政年份:2014
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:8850849
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项目类别:
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资助金额:$34.94万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:8662251
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项目类别:
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资助金额:$34.94万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:8463520
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项目类别:
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资助金额:$33.72万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:9232142
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项目类别:
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资助金额:$62.99万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:8187518
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项目类别:
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资助金额:$40.12万
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财政年份:2011
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:9106923
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项目类别:
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资助金额:$63.71万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:8296549
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项目类别:
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资助金额:$34.94万
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财政年份:2011
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负责人:Wolfram Goessling
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依托单位:
PGE2 and wnt signaling during zebrafish liver development and regeneration
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批准号:8034236
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项目类别:
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资助金额:$8.82万
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财政年份:2010
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负责人:Wolfram Goessling
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依托单位:
Estrogen Regulation of Hepatic Growth
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批准号:9910380
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项目类别:
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资助金额:$62.99万
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财政年份:2010
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负责人:Wolfram Goessling
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依托单位:
PGE2 and wnt signaling during zebrafish liver development and regeneration
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项目类别:
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资助金额:$8.9万
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财政年份:2010
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负责人:Wolfram Goessling
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wnt Signaling in Liver Development and Disease
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资助金额:$13.31万
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财政年份:2005
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负责人:Wolfram Goessling
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依托单位:
海外基金