DNA methyltransferase inhibitors increase baculovirus-mediated gene expression in mammalian cells when applied before infection

The application of baculovirus as a gene delivery vector for mammalian cells is limited by gene silencing in host cells. Although histone deacetylation inhibitors were known to improve baculovirus-mediated gene expression in mammalian cells, another group of chemicals that induces epigenetic changes, DNA methyltransferase inhibitors (DNMTis), were reported to have no such effect. In the current work, we found that, when added prior to virus inoculation, DNMTis improved baculovirus-mediated gene expression by fourfold or more in all four mammalian cell lines tested. The presence of inhibitors during the period of virus inoculation was important for them to be effective.     

Post-transcriptional control of gene expression: bacterial mRNA degradation

Many biological processes cannot be fully understood without detailed knowledge of RNA metabolism. The continuous breakdown and resynthesis of prokaryotic mRNA permit rapid production of new kinds of proteins. In this way, mRNA levels can regulate protein synthesis and cellular growth. Analysing mRNA degradation in prokaryotes has been particularly difficult because most mRNA undergo rapid exponential decay. Prokaryotic mRNAs differ in their susceptibility to degradation by endonucleases and exonucleases, possibly because of variation in their sequencing and structure. In spite of numerous studies, details of mRNA degradation are still largely unknown. This review highlights those aspects of mRNA metabolism which seem most influential in the regulation of gene expression.