Abstract
It has been more than 50 years since the discovery of dinucleoside polyphosphates (Np(n)Ns) and yet their roles and mechanisms of action remain unclear. Here, we show that both methylated and non-methylated Np(n)Ns serve as RNA caps in Escherichia coli. Np(n)Ns are excellent substrates for T7 and E. coli RNA polymerases (RNAPs) and efficiently initiate transcription. We demonstrate, that the E. coli enzymes RNA 5'-pyrophosphohydrolase (RppH) and bis(5'-nucleosyl)-tetraphosphatase (ApaH) are able to remove the Np(n)N-caps from RNA. ApaH is able to cleave all Np(n)N-caps, while RppH is unable to cleave the methylated forms suggesting that the methylation adds an additional layer to RNA stability regulation. Our work introduces a different perspective on the chemical structure of RNA in prokaryotes and on the role of RNA caps. We bring evidence that small molecules, such as Np(n)Ns are incorporated into RNA and may thus influence the cellular metabolism and RNA turnover.