Single-cell DNA Methylome and 3D Multi-omic Atlas of the Adult Mouse Brain

Liu, H.; Zeng, Q.; Zhou, J.; Bartlett, A.; Wang, B.-A.; Berube, P.; Tian, W.; Kenworthy, M.; Altshul, J.; Nery, J. R.; Chen, H.; Castanon, R. G.; Zu, S.; Li, Y. E.; Lucero, J.; Osteen, J. K.; Pinto-Duarte, A.; Lee, J.; Rink, J.; Cho, S.; Emerson, N.; Nunn, M.; O'Connor, C.; Yao, Z.; Tasic, B.; Smith, K. A.; Zeng, H.; Luo, C.; Dixon, J. R.; Ren, B.; Behrens, M. M.; Ecker, J. R.

doi:10.1101/2023.04.16.536509

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bioRxiv · 10.1101/2023.04.16.536509

Single-cell DNA Methylome and 3D Multi-omic Atlas of the Adult Mouse Brain

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Abstract

Cytosine DNA methylation is essential in brain development and has been implicated in various neurological disorders. A comprehensive understanding of DNA methylation diversity across the entire brain in the context of the brains 3D spatial organization is essential for building a complete molecular atlas of brain cell types and understanding their gene regulatory landscapes. To this end, we employed optimized single-nucleus methylome (snmC-seq3) and multi-omic (snm3C-seq1) sequencing technologies to generate 301,626 methylomes and 176,003 chromatin conformation/methylome joint profiles from 117 dissected regions throughout the adult mouse brain. Using iterative clustering and integrating with companion whole-brain transcriptome and chromatin accessibility datasets, we constructed a methylation-based cell type taxonomy that contains 4,673 cell groups and 261 cross-modality-annotated subclasses. We identified millions of differentially methylated regions (DMRs) across the genome, representing potential gene regulation elements. Notably, we observed spatial cytosine methylation patterns on both genes and regulatory elements in cell types within and across brain regions. Brain-wide multiplexed error-robust fluorescence in situ hybridization (MERFISH2) data validated the association of this spatial epigenetic diversity with transcription and allowed the mapping of the DNA methylation and topology information into anatomical structures more precisely than our dissections. Furthermore, multi-scale chromatin conformation diversities occur in important neuronal genes, highly associated with DNA methylation and transcription changes. Brain-wide cell type comparison allowed us to build a regulatory model for each gene, linking transcription factors, DMRs, chromatin contacts, and downstream genes to establish regulatory networks. Finally, intragenic DNA methylation and chromatin conformation patterns predicted alternative gene isoform expression observed in a companion whole-brain SMART-seq3 dataset. Our study establishes the first brain-wide, single-cell resolution DNA methylome and 3D multi-omic atlas, providing an unparalleled resource for comprehending the mouse brains cellular-spatial and regulatory genome diversity.

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Liu, H., Zeng, Q., Zhou, J., Bartlett, A., Wang, B.-A., Berube, P., Tian, W., Kenworthy, M., Altshul, J., Nery, J. R., Chen, H., Castanon, R. G., Zu, S., Li, Y. E., Lucero, J., Osteen, J. K., Pinto-Duarte, A., Lee, J., Rink, J., Cho, S., Emerson, N., Nunn, M., O'Connor, C., Yao, Z., Tasic, B., Smith, K. A., Zeng, H., Luo, C., Dixon, J. R., Ren, B., Behrens, M. M., Ecker, J. R.. 2023-04-18. Single-cell DNA Methylome and 3D Multi-omic Atlas of the Adult Mouse Brain. https://doi.org/10.1101/2023.04.16.536509

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