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Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease
- Source :
- Nature neuroscience, Nature reviews / Neuroscience 21(10), 1482-1492 (2018). doi:10.1038/s41593-018-0223-0
- Publication Year :
- 2018
-
Abstract
- Enhancers function as DNA logic gates and may control specialized functions of billions of neurons. Here we show a tailored program of noncoding genome elements active in situ in physiologically distinct dopamine neurons of the human brain. We found 71,022 transcribed noncoding elements, many of which were consistent with active enhancers and with regulatory mechanisms in zebrafish and mouse brains. Genetic variants associated with schizophrenia, addiction, and Parkinson’s dis- ease were enriched in these elements. Expression quantitative trait locus analysis revealed that Parkinson’s disease-associated variants on chromosome 17q21 cis-regulate the expression of an enhancer RNA in dopamine neurons. This study shows that enhancers in dopamine neurons link genetic variation to neuropsychiatric traits.
- Subjects :
- Male
0301 basic medicine
Quantitative Trait Loci
Enhancer RNAs
Biology
genetics [Mental Disorders]
Genome
Article
03 medical and health sciences
0302 clinical medicine
pathology [Brain]
Dopamine
ddc:570
medicine
Animals
Humans
physiology [Dopaminergic Neurons]
Enhancer
Zebrafish
Regulation of gene expression
genetics [Quantitative Trait Loci]
Dopaminergic Neurons
Mental Disorders
General Neuroscience
Brain
Genetic Variation
pathology [Mental Disorders]
genetics [Enhancer Elements, Genetic]
Human brain
biology.organism_classification
genetics [Genetic Variation]
3. Good health
Enhancer Elements, Genetic
030104 developmental biology
medicine.anatomical_structure
Gene Expression Regulation
Expression quantitative trait loci
Female
Neuroscience
030217 neurology & neurosurgery
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 15461726 and 10976256
- Volume :
- 21
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- Nature neuroscience
- Accession number :
- edsair.doi.dedup.....66117bcda544b47773643fbaa1f0d2ab