Neural and genetic basis of social behavior in cichlid fish
Neural and genetic basis of social behavior in cichlid fish
批准号:
9396183
负责人:
Nicole Marie Baran
金额:
$5.71万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2019-08-31
关键词:
Adaptive BehaviorsAfricaAggressive behaviorAllelesAnimal ModelBehaviorBehavior ControlBehavioralBehavioral AssayBehavioral ModelBehavioral ParadigmBiological ModelsBrainBrain regionCRISPR/Cas technologyCichlidsCodeComplexEmployee StrikesExhibitsFoundationsGene ExpressionGene Expression ProfileGene Expression RegulationGeneticGenetic ModelsGenetic PolymorphismGenomeGenomicsGoalsHealthHeritabilityHormone ReceptorHumanHybridsIndividualIntentionLeadLinkMalawiMapsMethodsMolecularNeuronsNeurosciencesPhenotypePopulationRadiationReceptor GeneRecruitment ActivityResearchRoleSilicon DioxideSocial BehaviorSystemTechnologyTerritorialityTestingVariantVasopressinsVertebratesbrain behaviordesignexperimental studygenetic variantgenome editinggenome wide association studyinsightinterdisciplinary approachneural circuitneuromechanismnovelreceptorrelating to nervous systemsocialspecies differencetranscriptome
中文摘要
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英文摘要
PROJECT SUMMARY:
The overarching goal of the proposed research is to investigate the neural and genetic basis of a
naturally-occurring difference in aggressive behavior. Aggression has a strong genetic
component, and yet we understand very little about how variation in the genome alters brain
function to produce changes in behavior. Most of what is known about the relationship between
genetic variants and social behavior comes from a small number of traditional lab model
organisms. Using a novel natural vertebrate system, we employ an interdisciplinary approach to
investigate the role of genetic polymorphisms in producing neural and behavioral variation. Rock-
and sand-dwelling cichlid fishes from Lake Malawi in East Africa are closely-related and their
genomes are very similar, yet they exhibit substantial diversity in social behaviors, including
aggression. In Aim 1, I will quantify differences in aggressive behavior between rock- and sand-
dwelling species and their hybrids. In Aim 2, I will first map the brain regions recruited during
aggression by visualizing the expression of a marker of neural activity. Secondly, I will
characterize the gene expression patterns of aggression-activated neurons by sequencing their
transcriptomes, allowing us to discover novel genetic variants associated with differences in
behavior. By comparing these results across species and their hybrids, we will provide insight into
the neural and genomic mechanisms underlying phenotypic variation in aggression. In Aim 3, we
will causally test the effect on brain and behavior of a candidate genetic variant in a vasopressin
hormone receptor gene via CRISPR-Cas9 genome editing technology. This integrative approach
is designed to provide insight into how variation in aggression can be produced by small changes
to the sequence or regulation of genes. Taken together, this strategy will identify how the neural
circuits regulating an essential social behavior are controlled at the level of the genome in outbred
vertebrates, providing a model of behavioral diversity in humans.
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