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The targeted cytosolic degradation of class I histone deacetylases is essential for efficient alphaherpesvirus replication

Ming, S.; Du, M.-H.; Yang, J.-M.; Guo, Y.-D.; Pan, J.-J.; Lu, W.-F.; Wang, J.; Zeng, L.; Chu, B.-B.

2026-01-02 cell biology
10.64898/2026.01.02.697337 bioRxiv
Show abstract

Viral infection triggers a robust DNA damage response (DDR), reshaping the host chromatin landscape to facilitate viral replication. Here, we uncover a novel mechanism by which alphaherpesviruses exploit the DDR pathway. We demonstrated that herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV) induced selective degradation of class I histone deacetylases (HDAC1/2), leading to histone hyperacetylation and subsequent DDR activation. Strikingly, viral infection promoted nuclear export of HDAC1/2, followed by MDM2-mediated K63-linked polyubiquitination and proteasomal degradation in the cytoplasm. Pharmacological inhibition of either DDR signaling or HDAC1/2 nuclear export significantly affected viral replication in vitro and in vivo. Our findings reveal a unique viral strategy to hijack host epigenetic regulation for efficient replication and identify potential therapeutic targets for alphaherpesvirus infections.

Published in eLife (predicted rank #2) · training set

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