1/2 Identification and Validation of Expression Quantitative Trait Loci (eQTLs) in discrete cell types across human brain development
1/2 Identification and Validation of Expression Quantitative Trait Loci (eQTLs) in discrete cell types across human brain development
批准号:
9948364
负责人:
NENAD SESTAN
金额:
$68.82万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-02-01 至 2025-11-30
关键词:
AdolescenceAdultAffectAge of OnsetAllelesAlzheimer&aposs DiseaseBehaviorBiologicalBipolar DisorderBrainBrain regionCell NucleusCellsChromatinCodeCommunitiesComplementCopy Number PolymorphismCorpus striatum structureDNADataData SetDatabasesDevelopmentDiseaseEpigenetic ProcessEtiologyExhibitsFetal DevelopmentFoundationsGene ExpressionGene Expression ProfileGene FrequencyGenerationsGenesGeneticGenotypeHumanHuman GenomeIndividualLinkMethodsNeurobiologyNeurodevelopmental DisorderNeurosciencesPatternPrefrontal CortexPrevalenceProcessPropertyProteinsQuantitative Trait LociRNA SplicingRegulatory ElementResourcesRiskRoleSamplingSchizophreniaSingle Nucleotide PolymorphismSmall Nuclear RNASourceSpecificitySpliced GenesStructureSystemTissuesUntranslated RNAValidationVariantautism spectrum disorderbrain cellbrain tissuecell typecohortcomputerized toolsdisorder riskepigenetic markerexperimental studyfetalfunctional genomicsgenetic risk factorgenetic variantgenome sequencinggenome wide association studygenomic datagenomic locusgenomic variationhistone modificationinsertion/deletion mutationinsightneurodevelopmentneuropsychiatric disordernext generationnovelpostnatal developmentprenatalrare variantrisk variantsexspatiotemporaltraittranscriptometranscriptome sequencingwhole genome
中文摘要
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英文摘要
ABSTRACT
Functional genomic analyses of the developing human brain have revealed highly dynamic spatiotemporal
patterns of gene expression and epigenetic changes during prenatal and early postnatal development and across
brain regions. Disruptions of these developmentally dynamic processes have been implicated by numerous
complementary analyses in the etiology of multiple neurodevelopmental and neuropsychiatric disorders.
Expression quantitative trait loci (eQTLs), along with splicing quantitative trait loci (sQTLs) and structural variant
quantitative trait loci (svQTLs), are genomic variants that differ between individuals, with these differences
correlating with functional changes to gene expression or splicing behavior. Many of these QTLs show specificity
to tissues, brain regions, developmental stages, or cell types, and a proportion overlap with known genetic risk
factors of human disorders. Here, we propose to pursue three integrated Aims, including whole-genome
sequencing and both bulk tissue and single-nuclei RNA sequencing, to identify genomic variants,
eQTL/sQTL/svQTLs, and patterns of gene expression and co-expression in two regions of the human brain
across mid-fetal development through to adolescence. In addition, we will apply novel and newly developed
computational tools to associate these QTLs with specific cell types and loci or genes implicated in
neuropsychiatric disorders. By so doing we will augment, and dramatically expand upon, earlier efforts to
understand QTLs and their roles in neural development, function, and neuropsychiatric disorders.
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