Identification of the Promoter Antisense Transcript Enhancing the Transcription of the Equine Herpesvirus-1 Immediate-Early Gene

被引:0
|
作者
Maeda, Mayuko [1 ]
Abe, Miou [1 ]
Aoshima, Keisuke [1 ]
Kobayashi, Atsushi [1 ]
Fukushi, Hideto [2 ]
Kimura, Takashi [1 ]
机构
[1] Hokkaido Univ, Fac Vet Med, Lab Comparat Pathol, Sapporo 0600818, Japan
[2] Gifu Univ, Fac Appl Biol Sci, Lab Vet Microbiol, Gifu 5011193, Japan
来源
VIRUSES-BASEL | 2024年 / 16卷 / 08期
关键词
equine herpesvirus-1; gene expression; non-coding RNA; LONG NONCODING RNAS; SIMPLEX-VIRUS VP16; TYPE-1; PROTEIN; EXPRESSION; MICRORNAS; HOMOLOG; LATENCY; GROWTH;
D O I
10.3390/v16081195
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Equine herpesvirus-1 (EHV-1) causes respiratory diseases, abortion, and encephalomyelitis in horses. The EHV-1 immediate-early (IE) protein, essential for viral replication, is transactivated by the binding of a multiprotein complex including the open reading frame 12 (ORF12) and some host factors to the IE promoter region. Promoter-associated non-coding RNAs (pancRNAs), which are transcribed from bidirectional promoters, regulate the transcription of neighboring genes in mammals and pathogens. In this study, we identified a novel pancRNA transcribed from across the areas of the 5 '-untranslated region and a promoter of EHV-1 IE and named it IE pancRNA. IE pancRNA and mRNA were simultaneously expressed in EHV-1-infected RN33B-A68B2M cells. This pancRNA was also transcribed in RK13 and E. Derm cells, which are highly susceptible to EHV-1 infection. Furthermore, IE pancRNA upregulated IE gene expression in the presence of ORF12, and stable expression of IE pancRNA increased the number of EHV-1-infected RN33B-A68B2M cells. These results suggest that IE pancRNAs facilitate EHV-1 proliferation by promoting IE gene expression.
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页数:13
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