| Literature DB >> 29312300 |
Lin Chen1,2, Chengmin Wang1, Jing Luo1, Wen Su1,2, Meng Li1,2, Na Zhao1,2, Wenting Lyu1,2, Hamidreza Attaran1, Yapeng He1, Hua Ding3, Hongxuan He1.
Abstract
Influenza A viruses (IAVs) take advantage of the host acetylation system for their own benefit. Whether the nucleoprotein (NP) of IAVs undergoes acetylation and the interaction between the NP and the class I histone deacetylases (HDACs) were largely unknown. Here, we showed that the NP protein of IAV interacted with HDAC1, which downregulated the acetylation level of NP. Using mass spectrometry, we identified lysine 103 as an acetylation site of the NP. Compared with wild-type protein, two K103 NP mutants, K103A and K103R, enhanced replication efficiency of the recombinant viruses in vitro. We further demonstrated that HDAC1 facilitated viral replication via two paths: promoting the nuclear retention of NP and inhibiting TBK1-IRF3 pathway. Our results lead to a new mechanism for regulating NP acetylation, indicating that HDAC1 may be a possible target for antiviral drugs.Entities:
Keywords: deacetylation; histone deacetylase 1; influenza A virus; nucleoprotein; type I interferon
Year: 2017 PMID: 29312300 PMCID: PMC5733105 DOI: 10.3389/fimmu.2017.01757
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561