Inhibition of post-transcriptional RNA processing by CDK inhibitors and its implication in anti-viral therapy
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
G0700142
Medical Research Council - United Kingdom
G1000236
Medical Research Council - United Kingdom
MR/L018373/1
Medical Research Council - United Kingdom
PubMed
24586613
PubMed Central
PMC3931720
DOI
10.1371/journal.pone.0089228
PII: PONE-D-13-41011
Knihovny.cz E-zdroje
- MeSH
- buněčné linie MeSH
- buněčný cyklus účinky léků MeSH
- Cercopithecus aethiops MeSH
- cyklin-dependentní kinasy antagonisté a inhibitory MeSH
- DNA virů MeSH
- fosforylace účinky léků MeSH
- inhibitory proteinkinas farmakologie MeSH
- ledviny účinky léků metabolismus MeSH
- lidé MeSH
- posttranskripční úpravy RNA účinky léků MeSH
- promotorové oblasti (genetika) účinky léků MeSH
- puriny farmakologie MeSH
- RNA-polymerasa II genetika metabolismus MeSH
- roskovitin MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cyklin-dependentní kinasy MeSH
- DNA virů MeSH
- inhibitory proteinkinas MeSH
- olomoucine II MeSH Prohlížeč
- puriny MeSH
- RNA-polymerasa II MeSH
- roskovitin MeSH
Cyclin-dependent kinases (CDKs) are key regulators of the cell cycle and RNA polymerase II mediated transcription. Several pharmacological CDK inhibitors are currently in clinical trials as potential cancer therapeutics and some of them also exhibit antiviral effects. Olomoucine II and roscovitine, purine-based inhibitors of CDKs, were described as effective antiviral agents that inhibit replication of a broad range of wild type human viruses. Olomoucine II and roscovitine show high selectivity for CDK7 and CDK9, with important functions in the regulation of RNA polymerase II transcription. RNA polymerase II is necessary for viral transcription and following replication in cells. We analyzed the effect of inhibition of CDKs by olomoucine II on gene expression from viral promoters and compared its effect to widely-used roscovitine. We found that both roscovitine and olomoucine II blocked the phosphorylation of RNA polymerase II C-terminal domain. However the repression of genes regulated by viral promoters was strongly dependent on gene localization. Both roscovitine and olomoucine II inhibited expression only when the viral promoter was not integrated into chromosomal DNA. In contrast, treatment of cells with genome-integrated viral promoters increased their expression even though there was decreased phosphorylation of the C-terminal domain of RNA polymerase II. To define the mechanism responsible for decreased gene expression after pharmacological CDK inhibitor treatment, the level of mRNA transcription from extrachromosomal DNA was determined. Interestingly, our results showed that inhibition of RNA polymerase II C-terminal domain phosphorylation increased the number of transcribed mRNAs. However, some of these mRNAs were truncated and lacked polyadenylation, which resulted in decreased translation. These results suggest that phosphorylation of RNA polymerase II C-terminal domain is critical for linking transcription and posttrancriptional processing of mRNA expressed from extrachromosomal DNA.
Regional Centre for Applied Molecular Oncology Masaryk Memorial Cancer Institute Brno Czech Republic
School of Medicine Cardiff University Cardiff United Kingdom
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