| Literature DB >> 24606677 |
Paul Lawrence1, Joseph S Conderino1, Elizabeth Rieder2.
Abstract
Previously, RNA helicase A (RHA) re-localization from the nucleus to the cytoplasm in foot-and-mouth disease virus (FMDV) infected cells was shown to coincide with loss of RHA methylated arginine residues at its C-terminus. The potential interaction between RHA and Jumonji C-domain (JmjC) protein 6 (JMJD6) arginine demethylase in infected cells was investigated. Treatment with N-oxalylglycine (NOG) inhibitor of JmjC demethylases prevented FMDV-induced RHA demethylation and re-localization, and also decreased viral protein synthesis and virus titers. Physical interaction between JMJD6 and RHA was demonstrated via reciprocal co-immunoprecipitation, where RHA preferentially bound JMJD6 monomers. Nuclear efflux of demethylated RHA (DM-RHA) coincided with nuclear influx of JMJD6, which was not observed using another picornavirus. A modified biochemical assay demonstrated JMJD6 induced dose-dependent demethylation of RHA and two RHA-derived isoforms, which could be inhibited by NOG. We propose a role for JMJD6 in RHA demethylation stimulated by FMDV, that appears to facilitate virus replication. Published by Elsevier Inc.Entities:
Keywords: Arginine demethylation; Foot-and-mouth disease virus (FMDV); Jumonji C-domain containing protein 6 (JMJD6); RNA helicase A (RHA)
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Year: 2014 PMID: 24606677 DOI: 10.1016/j.virol.2013.12.040
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616