Single-cell DNA methylation and 3D genome architecture in the human brain.
Wei TianJingtian ZhouAnna BartlettQiurui ZengHanqing LiuRosa Gomez CastanonMia KenworthyJordan AltshulCynthia ValadonAndrew I AldridgeJoseph R NeryHuaming ChenJiaying XuNicholas D JohnsonJacinta LuceroJulia K OsteenNora EmersonJonathan A RinkJasper LeeYang Eric LiKimberly SilettiMichelle LiemNaomi ClaffeyCarolyn O'ConnorAnna Marie YannyJulie NyhusNick DeeTamara CasperNadiya V ShapovalovaDaniel HirschsteinSong-Lin DingRebecca D HodgeBoaz P LeviC Dirk KeeneSten LinnarssonEd S LeinBing RenM Margarita BehrensJoseph R EckerPublished in: Science (New York, N.Y.) (2023)
Delineating the gene-regulatory programs underlying complex cell types is fundamental for understanding brain function in health and disease. Here, we comprehensively examined human brain cell epigenomes by probing DNA methylation and chromatin conformation at single-cell resolution in 517 thousand cells (399 thousand neurons and 118 thousand non-neurons) from 46 regions of three adult male brains. We identified 188 cell types and characterized their molecular signatures. Integrative analyses revealed concordant changes in DNA methylation, chromatin accessibility, chromatin organization, and gene expression across cell types, cortical areas, and basal ganglia structures. We further developed single-cell methylation barcodes that reliably predict brain cell types using the methylation status of select genomic sites. This multimodal epigenomic brain cell atlas provides new insights into the complexity of cell-type-specific gene regulation in adult human brains.
Keyphrases
- single cell
- dna methylation
- gene expression
- rna seq
- genome wide
- cell therapy
- high throughput
- dna damage
- public health
- transcription factor
- stem cells
- white matter
- induced apoptosis
- copy number
- high resolution
- oxidative stress
- multiple sclerosis
- endothelial cells
- chronic pain
- bone marrow
- mental health
- endoplasmic reticulum stress
- subarachnoid hemorrhage