Long noncoding RNA U90926 is crucial for herpes simplex virus type 1 proliferation in murine retinal photoreceptor cells

Long non-coding RNAs (lncRNAs) play vital roles in the pathogenesis of infectious diseases, but the role of lncRNAs in herpes simplex virus 1 (HSV-1) infection remains unknown. Using RNA sequencing analysis, we explored lncRNAs that were highly expressed in murine retinal photoreceptor cell-derived...

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Veröffentlicht in:Scientific reports 2020-11, Vol.10 (1), p.19406-19406, Article 19406
Hauptverfasser: Shirahama, Shintaro, Onoguchi-Mizutani, Rena, Kawata, Kentaro, Taniue, Kenzui, Miki, Atsuko, Kato, Akihisa, Kawaguchi, Yasushi, Tanaka, Rie, Kaburaki, Toshikatsu, Kawashima, Hidetoshi, Urade, Yoshihiro, Aihara, Makoto, Akimitsu, Nobuyoshi
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Sprache:eng
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Zusammenfassung:Long non-coding RNAs (lncRNAs) play vital roles in the pathogenesis of infectious diseases, but the role of lncRNAs in herpes simplex virus 1 (HSV-1) infection remains unknown. Using RNA sequencing analysis, we explored lncRNAs that were highly expressed in murine retinal photoreceptor cell-derived 661W cells infected with HSV-1. U90926 RNA (522 nucleotides) was the most upregulated lncRNA detected post HSV-1 infection. The level of U90926 RNA was continuously increased post HSV-1 infection, reaching a 100-fold increase at 24 h. Cellular fractionation showed that U90926 RNA was located in the nucleus post HSV-1 infection. Downregulation of U90926 expression by RNA interference markedly suppressed HSV-1 DNA replication (80% reduction at 12 h post infection) and HSV-1 proliferation (93% reduction at 12 h post infection) in 661W cells. The survival rates of U90926 -knockdown cells were significantly increased compared to those of control cells (81% and 21%, respectively; p  
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-020-76450-2