An atlas of gene regulatory elements in adult mouse cerebrum

Yang Eric Li(Ludwig Cancer Research), Sebastian Preißl(University of California San Diego), Xiaomeng Hou(University of California San Diego), Ziyang Zhang(Ludwig Cancer Research), Kai Zhang(Ludwig Cancer Research), Yunjiang Qiu(Ludwig Cancer Research), Olivier Poirion(University of California San Diego), Bin Li(Ludwig Cancer Research), Joshua Chiou(University of California San Diego), Hanqing Liu(Salk Institute for Biological Studies), António Pinto‐Duarte(Salk Institute for Biological Studies), Naoki Kubo(Ludwig Cancer Research), Xiaoyu Yang(University of California, San Francisco), Rongxin Fang(Ludwig Cancer Research), Xinxin Wang(University of California San Diego), Jee Yun Han(University of California San Diego), Jacinta Lucero(Salk Institute for Biological Studies), Yiming Yan(Ludwig Cancer Research), Michael Miller(University of California San Diego), Samantha Kuan(Ludwig Cancer Research), David U. Gorkin(University of California San Diego), Kyle J. Gaulton(University of California San Diego), Yin Shen(University of California, San Francisco), Michael Nunn(Salk Institute for Biological Studies), Eran A. Mukamel(University of California San Diego), M. Margarita Behrens(Salk Institute for Biological Studies), Joseph R. Ecker(Salk Institute for Biological Studies), Bing Ren(Ludwig Cancer Research)
Nature
October 6, 2021
Cited by 204Open Access
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Abstract

Abstract The mammalian cerebrum performs high-level sensory perception, motor control and cognitive functions through highly specialized cortical and subcortical structures 1 . Recent surveys of mouse and human brains with single-cell transcriptomics 2–6 and high-throughput imaging technologies 7,8 have uncovered hundreds of neural cell types distributed in different brain regions, but the transcriptional regulatory programs that are responsible for the unique identity and function of each cell type remain unknown. Here we probe the accessible chromatin in more than 800,000 individual nuclei from 45 regions that span the adult mouse isocortex, olfactory bulb, hippocampus and cerebral nuclei, and use the resulting data to map the state of 491,818 candidate cis -regulatory DNA elements in 160 distinct cell types. We find high specificity of spatial distribution for not only excitatory neurons, but also most classes of inhibitory neurons and a subset of glial cell types. We characterize the gene regulatory sequences associated with the regional specificity within these cell types. We further link a considerable fraction of the cis -regulatory elements to putative target genes expressed in diverse cerebral cell types and predict transcriptional regulators that are involved in a broad spectrum of molecular and cellular pathways in different neuronal and glial cell populations. Our results provide a foundation for comprehensive analysis of gene regulatory programs of the mammalian brain and assist in the interpretation of noncoding risk variants associated with various neurological diseases and traits in humans.


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