Single-cell analysis of chromatin accessibility in the adult mouse brain

Zu, Songpeng and Li, Yang Eric and Wang, Kangli and Armand, Ethan J. and Mamde, Sainath and Amaral, Maria Luisa and Wang, Yuelai and Chu, Andre and Xie, Yang and Miller, Michael and Xu, Jie and Wang, Zhaoning and Zhang, Kai and Jia, Bojing and Hou, Xiaomeng and Lin, Lin and Yang, Qian and Lee, Seoyeon and Li, Bin and Kuan, Samantha and Liu, Hanqing and Zhou, Jingtian and Pinto-Duarte, Antonio and Lucero, Jacinta and Osteen, Julia and Nunn, Michael and Smith, Kimberly A. and Tasic, Bosiljka and Yao, Zizhen and Zeng, Hongkui and Wang, Zihan and Shang, Jingbo and Behrens, M. Margarita and Ecker, Joseph R. and Wang, Allen and Preissl, Sebastian and Ren, Bing (2023) Single-cell analysis of chromatin accessibility in the adult mouse brain. Nature, 624 (7991). pp. 378-389. ISSN 0028-0836

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Abstract

Recent advances in single-cell technologies have led to the discovery of thousands of brain cell types; however, our understanding of the gene regulatory programs in these cell types is far from complete1,2,3,4. Here we report a comprehensive atlas of candidate cis-regulatory DNA elements (cCREs) in the adult mouse brain, generated by analysing chromatin accessibility in 2.3 million individual brain cells from 117 anatomical dissections. The atlas includes approximately 1 million cCREs and their chromatin accessibility across 1,482 distinct brain cell populations, adding over 446,000 cCREs to the most recent such annotation in the mouse genome. The mouse brain cCREs are moderately conserved in the human brain. The mouse-specific cCREs—specifically, those identified from a subset of cortical excitatory neurons—are strongly enriched for transposable elements, suggesting a potential role for transposable elements in the emergence of new regulatory programs and neuronal diversity. Finally, we infer the gene regulatory networks in over 260 subclasses of mouse brain cells and develop deep-learning models to predict the activities of gene regulatory elements in different brain cell types from the DNA sequence alone. Our results provide a resource for the analysis of cell-type-specific gene regulation programs in both mouse and human brains.

Item Type: Article
Subjects: Eprint Open STM Press > Geological Science
Depositing User: Unnamed user with email admin@eprint.openstmpress.com
Date Deposited: 14 Dec 2023 10:53
Last Modified: 14 Dec 2023 10:53
URI: http://library.go4manusub.com/id/eprint/1941

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