| Literature DB >> 32056715 |
Aditi S Kesari1, Veronica J Heintz1, Shishir Poudyal2, Andrew S Miller2, Richard J Kuhn2, Douglas J LaCount3.
Abstract
Zika virus (ZIKV) nonstructural protein 5 (NS5) plays a critical role in viral RNA replication and mediates key virus-host cell interactions. As with other flavivirus NS5 proteins, ZIKV NS5 is primarily found in the nucleus. We previously reported that the NS5 protein of dengue virus, another flavivirus, localized to centrosomes during cell division. Here we show that ZIKV NS5 also relocalizes from the nucleus to centrosomes during mitosis. In infected cells with supernumerary centrosomes, NS5 was present at all centrosomes. Transient expression of NS5 in uninfected cells confirmed that centrosomal localization was independent of other viral proteins. Live-cell imaging demonstrated that NS5-GFP accumulated at centrosomes shortly after break down of nuclear membrane and remained there through mitosis. Cells expressing NS5-GFP took longer to complete mitosis than control cells. Finally, an analysis of ZIKV NS5 binding partners revealed several centrosomal proteins, providing potential direct links between NS5 and centrosomes.Entities:
Keywords: Centrosome; Flavivirus; Nonstructural protein NS5; RNA-Dependent RNA polymerase; Zika virus
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Year: 2019 PMID： 32056715 PMCID： PMC7216507 DOI： 10.1016/j.virol.2019.11.018
Source DB: PubMed Journal: Virology ISSN： 0042-6822 Impact factor: 3.513