A mechanism of nucleotide misincorporation during transcription due to template-strand misalignment

Mol Cell. 2006 Oct 20;24(2):245-55. doi: 10.1016/j.molcel.2006.08.014.

Abstract

Transcription errors by T7 RNA polymerase (RNAP) may occur as the result of a mechanism in which the template base two positions downstream of the 3' end of the RNA (the TSn+1 base) is utilized during two consecutive nucleotide-addition cycles. In the first cycle, misalignment of the template strand leads to incorporation of a nucleotide that is complementary to the TSn+1 base. In the second cycle, the template is realigned and the mismatched primer is efficiently extended, resulting in a substitution error. Proper organization of the transcription bubble is required for maintaining the correct register of the DNA template, as the presence of a complementary nontemplate strand opposite the TSn+1 base suppresses template misalignment. Our findings for T7 RNAP are in contrast to related DNA polymerases of the Pol I type, which fail to extend mismatches efficiently and generate predominantly deletion errors as a result of template-strand misalignment.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Base Pair Mismatch
  • Base Sequence
  • Binding Sites
  • DNA Repair
  • DNA-Directed DNA Polymerase / metabolism
  • DNA-Directed RNA Polymerases / chemistry
  • DNA-Directed RNA Polymerases / genetics*
  • DNA-Directed RNA Polymerases / metabolism*
  • Escherichia coli / genetics
  • Frameshift Mutation
  • Gene Deletion
  • Models, Genetic
  • Molecular Sequence Data
  • Protein Conformation
  • Time Factors
  • Transcription, Genetic*
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*
  • Viral Proteins / metabolism*

Substances

  • Viral Proteins
  • bacteriophage T7 RNA polymerase
  • DNA-Directed RNA Polymerases
  • DNA-Directed DNA Polymerase