@Article{Friedl2022,
  author          = {Friedl, Marie-Sophie and Djakovic, Lara and Kluge, Michael and Hennig, Thomas and Whisnant, Adam W. and Backes, Simone and Dölken, Lars and Friedel, Caroline C.},
  journal         = {PloS one},
  title           = {HSV-1 and influenza infection induce linear and circular splicing of the long NEAT1 isoform.},
  year            = {2022},
  issn            = {1932-6203},
  pages           = {e0276467},
  volume          = {17},
  abstract        = {The herpes simplex virus 1 (HSV-1) virion host shut-off (vhs) protein cleaves both cellular and viral mRNAs by a translation-initiation-dependent mechanism, which should spare circular RNAs (circRNAs). Here, we show that vhs-mediated degradation of linear mRNAs leads to an enrichment of circRNAs relative to linear mRNAs during HSV-1 infection. This was also observed in influenza A virus (IAV) infection, likely due to degradation of linear host mRNAs mediated by the IAV PA-X protein and cap-snatching RNA-dependent RNA polymerase. For most circRNAs, enrichment was not due to increased circRNA synthesis but due to a general loss of linear RNAs. In contrast, biogenesis of a circRNA originating from the long isoform (NEAT1_2) of the nuclear paraspeckle assembly transcript 1 (NEAT1) was induced both in HSV-1 infection-in a vhs-independent manner-and in IAV infection. This was associated with induction of novel linear splicing of NEAT1_2 both within and downstream of the circRNA. NEAT1_2 forms a scaffold for paraspeckles, nuclear bodies located in the interchromatin space, must likely remain unspliced for paraspeckle assembly and is up-regulated in HSV-1 and IAV infection. We show that NEAT1_2 splicing and up-regulation can be induced by ectopic co-expression of the HSV-1 immediate-early proteins ICP22 and ICP27, potentially linking increased expression and splicing of NEAT1_2. To identify other conditions with NEAT1_2 splicing, we performed a large-scale screen of published RNA-seq data. This uncovered both induction of NEAT1_2 splicing and poly(A) read-through similar to HSV-1 and IAV infection in cancer cells upon inhibition or knockdown of CDK7 or the MED1 subunit of the Mediator complex phosphorylated by CDK7. In summary, our study reveals induction of novel circular and linear NEAT1_2 splicing isoforms as a common characteristic of HSV-1 and IAV infection and highlights a potential role of CDK7 in HSV-1 or IAV infection.},
  chemicals       = {RNA, Circular, Immediate-Early Proteins, RNA, Messenger, Protein Isoforms, RNA-Dependent RNA Polymerase, Mediator Complex},
  citation-subset = {IM},
  completed       = {2022-10-26},
  country         = {United States},
  doi             = {10.1371/journal.pone.0276467},
  issn-linking    = {1932-6203},
  issue           = {10},
  keywords        = {Humans; Herpesvirus 1, Human, genetics; RNA, Circular; Immediate-Early Proteins, genetics; Influenza, Human; Herpes Simplex; RNA, Messenger, genetics; Protein Isoforms, genetics; RNA-Dependent RNA Polymerase; Mediator Complex},
  nlm-id          = {101285081},
  owner           = {NLM},
  pii             = {e0276467},
  pmc             = {PMC9591066},
  pmid            = {36279270},
  pubmodel        = {Electronic-eCollection},
  pubstate        = {epublish},
  revised         = {2022-10-28},
}