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Updated: Jun 7, 2025

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
Published on: September 20, 2018
Histone variant H2BE controls activity-dependent gene expression and homeostatic scaling
Emily R Feierman1,2,3, Alekh Paranjapye2,3, Steven Su2,3
1Neuroscience Graduate Group, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
The histone variant H2BE is crucial for neuronal function and memory. Its expression decreases with neuronal activity, and it is essential for long-term activity-dependent gene expression and plasticity.
Area of Science:
- Neuroscience
- Molecular Biology
- Epigenetics
Background:
- Cellular responses to stimuli involve transcriptional programs regulated by histone proteins.
- Histone variants, like H2B histone variant H2BE, play specific roles in gene regulation.
- H2BE was previously identified as promoting transcription and being vital for neuronal function and memory.
Purpose of the Study:
- To investigate how extracellular stimuli regulate H2BE expression.
- To determine if H2BE controls activity-dependent transcription and cellular plasticity in neurons.
- To understand the role of H2BE in homeostatic plasticity.
Main Methods:
- CUT&Tag and RNA-sequencing of primary neurons.
- Single-nucleus sequencing of cortical tissue.
- Multielectrode array recordings to assess neuronal activity and plasticity.
Main Results:
- H2BE expression is inversely correlated with neuronal activity.
- Neurons lacking H2BE exhibit impaired long-term activity-dependent transcriptional responses.
- H2BE knockout neurons fail to undergo homeostatic plasticity after prolonged stimulation.
Conclusions:
- H2BE is a key histone variant involved in neuronal plasticity.
- H2BE is necessary for long-term activity-dependent gene expression and homeostatic plasticity in neurons.
- This study reveals the first histone variant implicated in the homeostatic plasticity response in neurons.
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