- Luo, Chongyuan;
- Keown, Christopher L;
- Kurihara, Laurie;
- Zhou, Jingtian;
- He, Yupeng;
- Li, Junhao;
- Castanon, Rosa;
- Lucero, Jacinta;
- Nery, Joseph R;
- Sandoval, Justin P;
- Bui, Brian;
- Sejnowski, Terrence J;
- Harkins, Timothy T;
- Mukamel, Eran A;
- Behrens, M Margarita;
- Ecker, Joseph R
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.