@article{mbs:/content/journal/jgv/10.1099/jgv.0.000679, author = "Zheng, Kai and Jiang, Yingchun and He, Zhendan and Kitazato, Kaio and Wang, Yifei", title = "Cellular defence or viral assist: the dilemma of HDAC6", journal= "Journal of General Virology", year = "2017", volume = "98", number = "3", pages = "322-337", doi = "https://doi.org/10.1099/jgv.0.000679", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/jgv.0.000679", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", keywords = "HDAC6", keywords = "microtubule acetylation", keywords = "autophagy", keywords = "aggresome", keywords = "immune response", keywords = "therapeutic target", abstract = "Histone deacetylase 6 (HDAC6) is a unique cytoplasmic deacetylase that regulates various important biological processes by preventing protein aggregation and deacetylating different non-histone substrates including tubulin, heat shock protein 90, cortactin, retinoic acid inducible gene I and β-catenin. Growing evidence has indicated a dual role for HDAC6 in viral infection and pathogenesis: HDAC6 may represent a host defence mechanism against viral infection by modulating microtubule acetylation, triggering antiviral immune response and stimulating protective autophagy, or it may be hijacked by the virus to enhance proinflammatory response. In this review, we will highlight current data illustrating the complexity and importance of HDAC6 in viral pathogenesis. We will summarize the structure and functional specificity of HDAC6, and its deacetylase- and ubiquitin-dependent activity in key cellular events in response to virus infection. We will also discuss how HDAC6 exerts its direct or indirect histone modification ability in viral lytic–latency switch.", }