Using H-MAGMA to decipher neurobiological bases of smoking and alcohol use traits
Using H-MAGMA to decipher neurobiological bases of smoking and alcohol use traits
批准号:
10056376
负责人:
HYEJUNG WON
金额:
$21.57万
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:
已结题
起止时间:
2020-07-15 至 2022-06-30
关键词:
AddressAdultAffectAlcohol consumptionAlcohol dependenceAlcoholsAstrocytesAtlasesBioinformaticsBiologicalBrainCellsChromatinChromosome MappingCigaretteCoupledDNAData SetDepositionDevelopmentDimensionsDiseaseExpression ProfilingGene Expression RegulationGenesGeneticGenomic SegmentGenomicsHeritabilityHuman GeneticsLightLinkMeasuresMethodsMolecularMorbidity - disease rateNatureNeurobiologyNeuronsNeurosciencesNicotineNicotine DependenceOntologyPathway interactionsPharmacological TreatmentPublicationsRegulator GenesRiskRisk FactorsSignal TransductionSmokingTestingTissuesUntranslated RNAVariantaddictionalcohol riskalcohol use disorderbasebrain cellcell typecigarette addictioncigarette smokingdisorder riskfetalgenetic risk factorgenome wide association studygenome-wideglobal healthimprovedinsightmortalityneurobiological mechanismnovelrisk variantsmoking cessationstatisticstooltraittranscriptomics
中文摘要
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英文摘要
PROJECT SUMMARY
Nicotine and alcohol dependence represent major global health concerns as leading causes of preventable
morbidity and mortality. Despite their global burden, pharmacological treatment options are limited, in large
part because their molecular mechanisms remain unclear. Cigarette smoking and alcohol use traits are
heritable, and genome-wide association studies (GWAS) have provided robust evidence for common variants
in nearly 400 genomic regions that influence smoking and/or alcohol use traits. However, the vast majority of
associated variants reside in non-coding DNA, and their target genes, gene networks, and relevant
neurobiological mechanisms are poorly understood. The critical first step of the proposal is to identify
neurobiologically-relevant target genes of known loci by applying H-MAGMA to a comprehensive set of large,
well-powered GWAS for smoking and alcohol use traits, including nicotine dependence (ND), cigarettes per
day (CPD), smoking cessation (CS), alcohol use disorder (AUD), and alcohol drinks per week (DPW). Once the
putative target genes are identified, we will characterize their (1) molecular function and biological pathways
using gene set enrichment analyses, (2) cellular expression profiles based on single cell transcriptomic
datasets, and (3) developmental expression trajectories based on temporal transcriptomic atlas. This will
refine the molecular mechanism, central cell type, and developmental window critical for using and developing
addiction to cigarette smoking and alcohol. Further, because we will use a coherent framework (H-MAGMA)
to decipher biological underpinnings of all five GWAS of smoking and alcohol use traits, our proposed study
will allow the systematic characterization and comparison of different GWAS. Our comparison will result in the
identification of pleiotropic genes associated with developing addiction to cigarette and alcohol, which would
reveal core mechanisms underlying addiction.
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Using H-MAGMA to decipher neurobiological bases of smoking and alcohol use traits
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批准号:10214583
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项目类别:
-
资助金额:$23.77万
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财政年份:2020
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负责人:HYEJUNG WON
-
依托单位:
Connecting gene regulatory mechanisms in human brain to psychiatric illness
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批准号:9730720
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项目类别:
-
资助金额:$24.9万
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财政年份:2018
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负责人:HYEJUNG WON
-
依托单位:
Connecting gene regulatory mechanisms in human brain to psychiatric illness
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批准号:9371822
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项目类别:
-
资助金额:$11.48万
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财政年份:2017
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负责人:HYEJUNG WON
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依托单位:
海外基金