학술논문

Association of OPRM1 Functional Coding Variant With Opioid Use Disorder
Document Type
article
Source
JAMA Psychiatry. 77(10)
Subject
Human Genome
Brain Disorders
Substance Misuse
Genetics
Drug Abuse (NIDA only)
Aetiology
2.1 Biological and endogenous factors
Mental health
Good Health and Well Being
Aged
Female
Genome-Wide Association Study
Humans
Male
Middle Aged
Opioid-Related Disorders
Receptors
Opioid
mu
United States
United States Department of Veterans Affairs
Neurosciences
Stem Cell Research
Stem Cell Research - Nonembryonic - Human
Biotechnology
Pediatric
1.1 Normal biological development and functioning
Underpinning research
Neurological
Animals
Autism Spectrum Disorder
Brain
Cerebral Cortex
Epigenesis
Genetic
Epigenomics
Evolution
Molecular
Gene Expression
Histone Code
Interneurons
Macaca mulatta
Neurons
Pan troglodytes
Primates
Regulatory Elements
Transcriptional
Regulatory Sequences
Nucleic Acid
Transcriptome
H3K27ac histone modification
regulatory elements
glutamatergic neurons
GABAergic neurons
primate evolution
Other Medical and Health Sciences
Psychology
Cognitive Sciences
Language
Abstract
The human cerebral cortex contains many cell types that likely underwent independent functional changes during evolution. However, cell-type-specific regulatory landscapes in the cortex remain largely unexplored. Here we report epigenomic and transcriptomic analyses of the two main cortical neuronal subtypes, glutamatergic projection neurons and GABAergic interneurons, in human, chimpanzee, and rhesus macaque. Using genome-wide profiling of the H3K27ac histone modification, we identify neuron-subtype-specific regulatory elements that previously went undetected in bulk brain tissue samples. Human-specific regulatory changes are uncovered in multiple genes, including those associated with language, autism spectrum disorder, and drug addiction. We observe preferential evolutionary divergence in neuron subtype-specific regulatory elements and show that a substantial fraction of pan-neuronal regulatory elements undergoes subtype-specific evolutionary changes. This study sheds light on the interplay between regulatory evolution and cell-type-dependent gene-expression programs, and provides a resource for further exploration of human brain evolution and function.