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Expression of pseudorabies virus-encoded long noncoding RNAs in epithelial cells and neurons. | LitMetric

Expression of pseudorabies virus-encoded long noncoding RNAs in epithelial cells and neurons.

J Neurovirol

State Key Laboratory of Agricultural Microbiology and Key Laboratory of Preventive Veterinary Medicine in Hubei Province, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China.

Published: October 2018

AI Article Synopsis

  • Long noncoding RNAs (lncRNAs) are crucial for regulating genome replication and gene expression in various biological contexts, and this study identified lncRNAs in pseudorabies virus (PRV)-infected PK-15 cells.
  • The researchers sequenced and analyzed large quantities of RNA from mock-infected and PRV-infected cells, discovering three new viral lncRNAs and significant changes in the expression of 6,478 host lncRNAs due to infection.
  • The study found that one specific viral lncRNA, LDI, potentially influences the expression of a key viral transcriptional activator, IE180, and characterized lncRNA activity in chicken dorsal root ganglia, indicating that PRV can produce lncRNAs in

Article Abstract

Long noncoding RNAs (lncRNAs) play important roles in regulating eukaryotic genome replication and gene expression in diverse biological systems. Here, we identified lncRNAs transcribed from pseudorabies virus (PRV)-infected PK-15 cells. Based on high-throughput sequencing data, we obtained 87,263,926 and 93,947,628 clean reads from mock-infected and PRV-infected PK-15 cells, respectively. Through a normalized analytic protocol, we identified three novel viral lncRNAs. According to an analysis of differential expression between the mock-infected and PRV-infected cells, 4151 host lncRNAs were significantly upregulated and 2327 host lncRNAs were significantly downregulated in the latter group. Viral lncRNAs and several host lncRNAs were verified by northern blotting and real-time PCR. The findings showed that the viral lncRNA LDI might regulate the expression of IE180, a potent transcriptional activator of viral genes. Furthermore, we characterized the expression of viral lncRNAs in a culture of infected primary chicken dorsal root ganglia (DRG). Collectively, the obtained data suggest that PRV generates lncRNAs in both epithelial cells and chick DRG neurons.

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Source
http://dx.doi.org/10.1007/s13365-018-0651-3DOI Listing

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