A human cell atlas of fetal chromatin accessibility.
Silvia DomckeAndrew J HillRiza M DazaJunyue CaoDiana R O'DayHannah A PlinerKimberly A AldingerDmitry PokholokFan ZhangJennifer H MilbankMichael A ZagerIan A GlassFrank J SteemersDaniel A DohertyCole TrapnellDarren A CusanovichJay ShendurePublished in: Science (New York, N.Y.) (2020)
The chromatin landscape underlying the specification of human cell types is of fundamental interest. We generated human cell atlases of chromatin accessibility and gene expression in fetal tissues. For chromatin accessibility, we devised a three-level combinatorial indexing assay and applied it to 53 samples representing 15 organs, profiling ~800,000 single cells. We leveraged cell types defined by gene expression to annotate these data and cataloged hundreds of thousands of candidate regulatory elements that exhibit cell type-specific chromatin accessibility. We investigated the properties of lineage-specific transcription factors (such as POU2F1 in neurons), organ-specific specializations of broadly distributed cell types (such as blood and endothelial), and cell type-specific enrichments of complex trait heritability. These data represent a rich resource for the exploration of in vivo human gene regulation in diverse tissues and cell types.
Keyphrases
- gene expression
- single cell
- endothelial cells
- transcription factor
- cell therapy
- dna damage
- genome wide
- dna methylation
- induced pluripotent stem cells
- high throughput
- stem cells
- induced apoptosis
- machine learning
- electronic health record
- mesenchymal stem cells
- oxidative stress
- cell proliferation
- signaling pathway
- spinal cord injury
- cell cycle arrest