Epigenomic and chromosomal architectural reconfiguration in developing human frontal cortex and hippocampus
Matthew G. Heffel, Jingtian ZhouiD, Yi ZhangiD, Dong-Sung LeeiD, Kangcheng HouiD, Oier Pastor-AlonsoiD, Kevin Daniel AbuhannaiD, Anthony D. SchmittiD, Terence LiiD, Maximilian HaeussleriD, Brittney D WickiD, Martin Jinye ZhangiD, Fangming XieiD, Ryan S. Ziffra, Eran A. MukameliD, Eleazar EskiniD, Bogdan PaşaniuciD, Joseph R. EckeriD, Jesse R. DixoniD, Tomasz Jan NowakowskiiD, Mercedes F. ParedesiD, Chongyuan LuoiD
Abstract
The human frontal cortex and hippocampus play critical roles in learning and cognition. We investigated the epigenomic and 3D chromatin conformational reorganization during the development of the frontal cortex and hippocampus, using more than 53,000 joint single-nucleus profiles of chromatin conformation and DNA methylation (sn-m3C-seq). The remodeling of DNA methylation predominantly occurs during late-gestational to early-infant development and is temporally separated from chromatin conformation dynamics. Neurons have a unique Domain-Dominant chromatin conformation that is different from the Compartment-Dominant conformation of glial cells and non-brain tissues. We reconstructed the regulatory programs of cell-type differentiation and found putatively causal common variants for schizophrenia strongly overlap with chromatin loop-connected, cell-type-specific regulatory regions. Our data demonstrate that single-cell 3D-regulome is an effective approach for dissecting neuropsychiatric risk loci.
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