| Literature DB >> 27501340 |
Ryo Horie1, Misako Yoneda2, Shotaro Uchida1, Hiroki Sato1, Chieko Kai1.
Abstract
Nipah virus (NiV) causes severe encephalitis in humans, with high mortality. NiV nonstructural C protein (NiV-C) is essential for its pathogenicity, but its functions are unclear. In this study, we focused on NiV-C trafficking in cells and found that it localizes predominantly in the cytoplasm but partly in the nucleus. An analysis of NiV-C mutants showed that amino acids 2, 21-24 and 110-139 of NiV-C are important for its localization in the cytoplasm. Inhibitor treatment indicates that the nuclear export determinant is not a classical CRM1-dependent nuclear export signal. We also determined that amino acids 60-75 and 72-75 were important for nuclear localization of NiV-C. Furthermore, NiV-C mutants that had lost their capacity for nuclear localization inhibited the interferon (IFN) response more strongly than complete NiV-C. These results indicate that the IFN-antagonist activity of NiV-C occurs in the cytoplasm.Entities:
Keywords: C protein; Nipah virus; Nuclear export signal; Nuclear localization signal; Subcellular localization
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Year: 2016 PMID: 27501340 DOI: 10.1016/j.virol.2016.07.013
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616