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-Structure paper
| Title | Mechanism of USP21 autoinhibition and histone H2AK119 deubiquitination. |
|---|---|
| Journal, issue, pages | Sci Adv, Vol. 11, Issue 41, Page eady2604, Year 2025 |
| Publish date | Oct 10, 2025 |
Authors | Sanim Rahman / Chad W Hicks / Alexander Gwizdala / Cynthia Wolberger / ![]() |
| PubMed Abstract | Monoubiquitinated histone H2A lysine 119 (H2AK119ub) is a modification associated with transcriptional silencing and heterochromatin formation. Ubiquitin-specific protease 21 (USP21), one of four ...Monoubiquitinated histone H2A lysine 119 (H2AK119ub) is a modification associated with transcriptional silencing and heterochromatin formation. Ubiquitin-specific protease 21 (USP21), one of four major H2AK119-specific deubiquitinating enzymes (DUBs), plays critical roles in diverse cellular processes. However, the mechanisms by which USP21 specifically deubiquitinates H2AK119ub and is regulated are unknown. We determined the cryo-EM structure of the USP21 catalytic domain bound to an H2AK119ub nucleosome, which revealed a recognition mode that differs from that of other H2AK119-specific DUBs. We unexpectedly found that the N-terminal IDR of USP21 inhibits the enzyme's activity. Using AlphaFold-Multimer to perform a virtual screen of USP21 interactors, we identified kinases that phosphorylate the USP21 IDR and thereby relieve autoinhibition. AlphaFold3 modeling of USP21 suggests a structural model for autoinhibition. AlphaFold analysis suggests that phosphorylation-regulated autoinhibition may be a feature of various USP enzymes. These findings shed light on the mechanisms of H2AK119 deubiquitination and reveal a previously unexplored mode of phosphorylation-dependent DUB autoregulation. |
External links | Sci Adv / PubMed:41071870 / PubMed Central |
| Methods | EM (single particle) |
| Resolution | 2.98 Å |
| Structure data | EMDB-49919, PDB-9ny4: |
| Source |
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Keywords | NUCLEAR PROTEIN / Deubiquitinase / DNA-binding protein / DNA |
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