# Poly ADP‐ribosylation regulates Arc expression and promotes adaptive stress-coping

**Authors:** Eliyahu Dahan, Leah Pergamenshik, Tze’ela Taub, Arthur Vovk, Jade Manier, Raphael Avneri, Elad Lax

PMC · DOI: 10.1007/s00213-025-06744-8 · Psychopharmacology · 2025-01-14

## TL;DR

This study shows that a process called PARylation helps regulate a gene called Arc, which is important for coping with stress in mice.

## Contribution

The study identifies PARylation as a novel regulator of Arc expression and stress-coping behavior in response to acute stress.

## Key findings

- PARylation increases after acute stress and upregulates activity-dependent genes.
- Inhibiting PARP1 impairs stress-coping behavior and reduces Arc expression.
- PARylation at the Arc promoter affects histone H4 acetylation and Arc gene expression.

## Abstract

Rapid adaptation to stressful events is essential for survival and requires acute stress response and stress-coping strategy. However, the molecular mechanisms that govern this coping strategy have yet to be fully discovered.

This study aims to investigate the effects of poly ADP-ribosylation (PARylation) on stress-coping strategies following acute stress and to identify the target genes influenced by Parp1-induced histone PARylation.

Mice were subjected to a forced swim test, a well-established acute stress paradigm, to evaluate cortical PARylation and assess the expression of activity-dependent genes. The pharmacological inhibition of Parp1 was conducted using ABT888 (Veliparib) to determine its effects on stress-coping behavior and related molecular changes.

The forced swim test increased cortical PARylation and upregulated the expression of activity-dependent genes. Systemic inhibition of Parp1 with ABT888 led to impaired stress-coping behavior, evidenced by a reduced immobility response during a subsequent forced swim test done 24 hours later. This impairment was associated with decreased chromatin PARylation and histone H4 acetylation at the Arc promoter and reduced Arc expression observed one hour after Parp1 inhibition.

Our findings indicate that chromatin PARylation at the Arc promoters regulates histone H4 acetylation and Arc gene expression, and a subsequent impact on successful stress-coping behavior in response to acute stress.

The online version contains supplementary material available at 10.1007/s00213-025-06744-8.

## Linked entities

- **Genes:** ARC (activity regulated cytoskeleton associated protein) [NCBI Gene 23237]
- **Proteins:** PARP1 (poly(ADP-ribose) polymerase 1), HIS4 (histone H4)
- **Chemicals:** ABT888 (PubChem CID 11960529), Veliparib (PubChem CID 11960529)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** H4C6 (H4 clustered histone 6) [NCBI Gene 8361] {aka H4, H4/c, H4FC, HIST1H4F}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, ARC (activity regulated cytoskeleton associated protein) [NCBI Gene 23237] {aka Arg3.1, hArc}
- **Chemicals:** Poly ADP (-), ABT888 (MESH:C521013)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11890342/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC11890342/full.md

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Source: https://tomesphere.com/paper/PMC11890342