학술논문

An atlas of gene regulatory elements in adult mouse cerebrum
Document Type
article
Source
Nature. 598(7879)
Subject
Human Genome
Genetics
Biotechnology
Brain Disorders
Stem Cell Research - Nonembryonic - Non-Human
Stem Cell Research
Neurosciences
Underpinning research
1.1 Normal biological development and functioning
Neurological
Animals
Atlases as Topic
Cerebrum
Chromatin
Chromatin Assembly and Disassembly
Gene Expression Regulation
Genetic Predisposition to Disease
Humans
Male
Mice
Mice
Inbred C57BL
Nervous System Diseases
Neuroglia
Neurons
Regulatory Sequences
Nucleic Acid
Sequence Analysis
DNA
Single-Cell Analysis
General Science & Technology
Language
Abstract
The mammalian cerebrum performs high-level sensory perception, motor control and cognitive functions through highly specialized cortical and subcortical structures1. Recent surveys of mouse and human brains with single-cell transcriptomics2-6 and high-throughput imaging technologies7,8 have uncovered hundreds of neural cell types distributed in different brain regions, but the transcriptional regulatory programs that are responsible for the unique identity and function of each cell type remain unknown. Here we probe the accessible chromatin in more than 800,000 individual nuclei from 45 regions that span the adult mouse isocortex, olfactory bulb, hippocampus and cerebral nuclei, and use the resulting data to map the state of 491,818 candidate cis-regulatory DNA elements in 160 distinct cell types. We find high specificity of spatial distribution for not only excitatory neurons, but also most classes of inhibitory neurons and a subset of glial cell types. We characterize the gene regulatory sequences associated with the regional specificity within these cell types. We further link a considerable fraction of the cis-regulatory elements to putative target genes expressed in diverse cerebral cell types and predict transcriptional regulators that are involved in a broad spectrum of molecular and cellular pathways in different neuronal and glial cell populations. Our results provide a foundation for comprehensive analysis of gene regulatory programs of the mammalian brain and assist in the interpretation of noncoding risk variants associated with various neurological diseases and traits in humans.