Journal of Virology · 2018 · 56 citations · 38 references
Life SciencesMicrobiologyMolecular BiologyGene ExpressionMolecular VirologyVirologyAntiviral PharmacologyViral GeneticsViral InfectionsViral PathogenesisViral Rna BiologyViral TranscriptionAggresome FormationAntiviral Mechanisms Of ActionHost-targeted AntiviralsInfluenza Virus TranscriptionInfluenza Virus UncoatingRna Virus BiologyViral Polymerase InhibitorsViral Polymerases
Influenza A virus (IAV) continues to threaten global public health due to drug resistance and the emergence of frequently mutated strains. Thus, it is critical to find new strategies to control IAV infection. Here, we discover one host protein, HDAC6, that can inhibit viral RNA polymerase activity by deacetylating PA and thus suppresses virus RNA replication and transcription. Previously, it was reported that IAV can utilize the HDAC6-dependent aggresome formation mechanism to promote virus uncoating, but HDAC6-mediated deacetylation of α-tubulin inhibits viral protein trafficking at late stages of the virus life cycle. These findings together will contribute to a better understanding of the role of HDAC6 in regulating IAV infection. Understanding the molecular mechanisms of HDAC6 at various periods of viral infection may illuminate novel strategies for developing antiviral drugs.
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HDAC6 is a microtubule-associated deacetylase
Charlotte Hubbert, Amaris R. Guardiola, Rong Shao et al. · Nature · 2002 · 2.4K citations
HDAC6 Modulates Cell Motility by Altering the Acetylation Level of Cortactin
Xiaohong Zhang, Zhigang Yuan, Yingtao Zhang et al. · Molecular Cell · 2007 · 725 citations · Full text