Dinucleoside Polyphosphates as RNA Building Blocks with Pairing Ability in Transcription Initiation

ACS Chem Biol. 2020 Jul 17;15(7):1765-1772. doi: 10.1021/acschembio.0c00178. Epub 2020 Jun 18.

Abstract

Dinucleoside polyphosphates (NpnNs) were discovered 50 years ago in all cells. They are often called alarmones, even though the molecular target of the alarm has not yet been identified. Recently, we showed that they serve as noncanonical initiating nucleotides (NCINs) and fulfill the role of 5' RNA caps in Escherichia coli. Here, we present molecular insight into their ability to be used as NCINs by T7 RNA polymerase in the initiation phase of transcription. In general, we observed NpnNs to be equally good substrates as canonical nucleotides for T7 RNA polymerase. Surprisingly, the incorporation of ApnGs boosts the production of RNA 10-fold. This behavior is due to the pairing ability of both purine moieties with the -1 and +1 positions of the antisense DNA strand. Molecular dynamic simulations revealed noncanonical pairing of adenosine with the thymine of the DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriophage T7 / enzymology
  • Base Pairing
  • DNA / metabolism
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism
  • Dinucleoside Phosphates / genetics*
  • Dinucleoside Phosphates / metabolism
  • Molecular Dynamics Simulation
  • Protein Binding
  • RNA / genetics*
  • RNA / metabolism
  • RNA Caps / genetics
  • Transcription Initiation, Genetic*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism

Substances

  • Dinucleoside Phosphates
  • RNA Caps
  • Viral Proteins
  • RNA
  • DNA
  • bacteriophage T7 RNA polymerase
  • DNA-Directed RNA Polymerases