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Different Neuronal Activity Patterns Induce Different Gene Expression Programs
Open accessPublished version of a preprint
Abstract
A vast number of different neuronal activity patterns could each induce a different set of activity-regulated genes. Mapping this coupling between activity pattern and gene induction would allow inference of a neuron's activity-pattern history from its gene expression and improve our understanding of activity-pattern-dependent synaptic plasticity. In genome-scale experiments comparing brief and sustained activity patterns, we reveal that activity-duration history can be inferred from gene expression profiles. Brief activity selectively induces a small subset of the activity-regulated gene program that corresponds to the first of three temporal waves of genes induced by sustained activity. Induction of these first-wave genes is mechanistically distinct from that of the later waves because it requires MAPK/ERK signaling but does not require de novo translation. Thus, the same mechanisms that establish the multi-wave temporal structure of gene induction also enable different gene sets to be induced by different activity durations.
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“whereas maximum Bdnf upregulation occurred after 6 h”
From Three-dimensional genome restructuring across timescales of activity-induced neuronal gene expression (2020) · cites this paper as [9]
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“we re-analyzed a recently published RNA-seq time course during pharmacological neuronal activation9 and found maximum activation of the IEGs Fos and Arc by 60 min”
From Three-dimensional genome restructuring across timescales of activity-induced neuronal gene expression (2020) · cites this paper as [9]
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Metadata
- Authors
- Tyssowski, K. M., DeStefino, N. R., Cho, J.-H., Dunn, C. J., Poston, R. G., Carty, C. E., Jones, R. D., Chang, S. M., Romeo, P., Wurzelmann, M. K., Ward, J. M., Andermann, M. L., Saha, R. N., Dudek, S. M., & Gray, J. M.
- Affiliations
- Harvard University (US)
- University of California, Merced (US)
- Beth Israel Deaconess Medical Center (US)
- National Institute of Environmental Health Sciences (US)
- National Institutes of Health (US)
- Corresponding author
- Saha, Ramendra N.
- Dudek, Serena M.
- Gray, Jesse M.
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2018-05
- Volume
- 98
- Issue
- 3
- Pages
- 530-546.e11
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC5934296
- OpenAlex
- W2950828985
- Cited by
- 390
- References
- 177
- Citations by year
- 2026: 39 · 2025: 51 · 2024: 67 · 2023: 54 · 2022: 50 · 2021: 41 · 2020: 39 · 2019: 34 · 2018: 14
- FWCI
- 14.57
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Armenise-Harvard (R01 MH101528-01, R01 MH116223-01)
- Kaneb family
- Intramural Research Program of the National Institute of Environmental Health Sciences
- National Institutes of Health (Z01 ES100221)
- NSF Graduate Research Fellowship Program (DGE1144152, DEG1745303)
- National Institute of Health NRSA (R00 MH096941)
- Canadian Institute of Health Research
- NIH New Innovator Award (DP2 DK105570, R01 DK109930)
- McKnight Scholar Award
- Harvard Brain Science Initiative Bipolar Disorder Seed Grant
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- neural activity patterns, activity duration, ERK signaling, synaptic plasticity, gene expression profiling
- MeSH terms
- Animals, Cells, Cultured, Cerebral Cortex, Female, Gene Expression Regulation, Male, Mice, Inbred C57BL, Mice, Inbred ICR, Neurons, Photic Stimulation, Rats, Sprague-Dawley, MAP Kinase Signaling System, Mice, Rats
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