The mechanism of preferential synthesis of poly[r(purine)] in the transcription of poly[d(purine)] . poly[d(pyrimidine)] by T. thermophilus RNA polymerase

J Biochem. 1981 May;89(5):1501-11. doi: 10.1093/oxfordjournals.jbchem.a133343.

Abstract

The mechanism of preferential transcription on poly[d(purine)] . poly[d(pyrimidine)] was investigated using RNA polymerase of T. thermophilus HB8. Though the machinery for initiation is lacking, the core enzyme has the latent ability to synthesize poly[r(pyrimidine)] as well as poly[r(purine)]. The holoenzyme can synthesize poly[r(purine)] in the usual manner. Poly[r(pyrimidine)] synthesis by the holoenzyme is, however, forbidden. These results suggest that the sigma factor plays a crucial role in this preferential transcription, and that this preferential transcription may be useful as a model for the sense strand recognition. Various results led us to the hypothesis that the high affinity site for the poly[d(pyrimidine)] strands on the enzyme plays a very important role.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Circular Dichroism
  • DNA-Directed RNA Polymerases / metabolism*
  • Dinucleoside Phosphates
  • Micromonosporaceae / enzymology*
  • Nucleosides / pharmacology
  • Oligonucleotides / pharmacology
  • Polydeoxyribonucleotides / metabolism*
  • Polymers
  • Polyribonucleotides / metabolism*
  • Purines / metabolism*
  • Pyrimidines / metabolism*
  • Sigma Factor / metabolism
  • Templates, Genetic
  • Transcription, Genetic* / drug effects

Substances

  • Dinucleoside Phosphates
  • Nucleosides
  • Oligonucleotides
  • Polydeoxyribonucleotides
  • Polymers
  • Polyribonucleotides
  • Purines
  • Pyrimidines
  • Sigma Factor
  • Adenosine Triphosphate
  • DNA-Directed RNA Polymerases