Activity‐regulated gene expression across cell types of the mouse hippocampus

Author:

Nelson Erik D.123ORCID,Maynard Kristen R.12ORCID,Nicholas Kyndall R.1ORCID,Tran Matthew N.1ORCID,Divecha Heena R.1ORCID,Collado‐Torres Leonardo1ORCID,Hicks Stephanie C.4ORCID,Martinowich Keri1245ORCID

Affiliation:

1. Lieber Institute for Brain Development, Johns Hopkins Medical Campus Baltimore Maryland USA

2. Department of Psychiatry and Behavioral Sciences Johns Hopkins University School of Medicine Baltimore Maryland USA

3. Department of Neuroscience Johns Hopkins University School of Medicine Baltimore Maryland USA

4. Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

5. The Kavli Neuroscience Discovery Institute, Johns Hopkins University Baltimore Maryland USA

Abstract

AbstractActivity‐regulated gene (ARG) expression patterns in the hippocampus (HPC) regulate synaptic plasticity, learning, and memory, and are linked to both risk and treatment responses for many neuropsychiatric disorders. The HPC contains discrete classes of neurons with specialized functions, but cell type‐specific activity‐regulated transcriptional programs are not well characterized. Here, we used single‐nucleus RNA‐sequencing (snRNA‐seq) in a mouse model of acute electroconvulsive seizures (ECS) to identify cell type‐specific molecular signatures associated with induced activity in HPC neurons. We used unsupervised clustering and a priori marker genes to computationally annotate 15,990 high‐quality HPC neuronal nuclei from N = 4 mice across all major HPC subregions and neuron types. Activity‐induced transcriptomic responses were divergent across neuron populations, with dentate granule cells being particularly responsive to activity. Differential expression analysis identified both upregulated and downregulated cell type‐specific gene sets in neurons following ECS. Within these gene sets, we identified enrichment of pathways associated with varying biological processes such as synapse organization, cellular signaling, and transcriptional regulation. Finally, we used matrix factorization to reveal continuous gene expression patterns differentially associated with cell type, ECS, and biological processes. This work provides a rich resource for interrogating activity‐regulated transcriptional responses in HPC neurons at single‐nuclei resolution in the context of ECS, which can provide biological insight into the roles of defined neuronal subtypes in HPC function.

Funder

Chan Zuckerberg Initiative

Lieber Institute for Brain Development

National Institutes of Health

Silicon Valley Community Foundation

Publisher

Wiley

Subject

Cognitive Neuroscience

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3