| Literature DB >> 28798132 |
Chongyuan Luo1,2, Christopher L Keown3, Laurie Kurihara4, Jingtian Zhou1,5, Yupeng He1,5, Junhao Li3, Rosa Castanon1, Jacinta Lucero6, Joseph R Nery1, Justin P Sandoval1, Brian Bui6, Terrence J Sejnowski2,6,7, Timothy T Harkins4, Eran A Mukamel8, M Margarita Behrens9, Joseph R Ecker10,2.
Abstract
The mammalian brain contains diverse neuronal types, yet we lack single-cell epigenomic assays that are able to identify and characterize them. DNA methylation is a stable epigenetic mark that distinguishes cell types and marks regulatory elements. We generated >6000 methylomes from single neuronal nuclei and used them to identify 16 mouse and 21 human neuronal subpopulations in the frontal cortex. CG and non-CG methylation exhibited cell type-specific distributions, and we identified regulatory elements with differential methylation across neuron types. Methylation signatures identified a layer 6 excitatory neuron subtype and a unique human parvalbumin-expressing inhibitory neuron subtype. We observed stronger cross-species conservation of regulatory elements in inhibitory neurons than in excitatory neurons. Single-nucleus methylomes expand the atlas of brain cell types and identify regulatory elements that drive conserved brain cell diversity.Entities:
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Year: 2017 PMID: 28798132 PMCID: PMC5570439 DOI: 10.1126/science.aan3351
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728