Antiviral activity of a purine synthesis enzyme reveals a key role of deamidation in regulating protein nuclear import.

Protein nuclear translocation is highly regulated and crucial for diverse biological processes. However, our understanding concerning protein nuclear import is incomplete. Here we report that a cellular purine synthesis enzyme inhibits protein nuclear import via deamidation. Employing human Kaposi's sarcoma-associated herpesvirus (KSHV) to probe the role of protein deamidation, we identified a purine synthesis enzyme, phosphoribosylformylglycinamidine synthetase (PFAS) that inhibits KSHV transcriptional activation. PFAS deamidates the replication transactivator (RTA), a transcription factor crucial for KSHV lytic replication. Mechanistically, deamidation of two asparagines flanking a positively charged nuclear localization signal impaired the binding of RTA to an importin β subunit, thus diminishing RTA nuclear localization and transcriptional activation. Finally, RTA proteins of all gamma herpesviruses appear to be regulated by PFAS-mediated deamidation. These findings uncover an unexpected function of a metabolic enzyme in restricting viral replication and a key role of deamidation in regulating protein nuclear import. Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

Citation

Junhua Li, Jun Zhao, Simin Xu, Shu Zhang, Junjie Zhang, Jun Xiao, Ruoyun Gao, Mao Tian, Yi Zeng, Katie Lee, Vera Tarakanova, Ke Lan, Hao Feng, Pinghui Feng. Antiviral activity of a purine synthesis enzyme reveals a key role of deamidation in regulating protein nuclear import. Science advances. 2019 Oct;5(10):eaaw7373

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PMID: 31633017

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