Functional evidence for a small and rigid active site in a high fidelity DNA polymerase: probing T7 DNA polymerase with variably sized base pairs

J Biol Chem. 2006 Jan 27;281(4):2289-95. doi: 10.1074/jbc.M510744200. Epub 2005 Nov 27.


Hypotheses on the origins of high fidelity in replicative DNA polymerases have recently focused on the importance of geometric or steric effects in this selectivity. Here we reported a systematic study of the effects of base pair size in T7 DNA polymerase (pol), the replicative enzyme for bacteriophage T7. We varied base pair size in very small (0.25 A) increments by use of a series of nonpolar thymidine shape mimics having gradually increasing size. Steady-state kinetics were evaluated for the 5A7A exonuclease-deficient mutant in a 1:1 complex with thioredoxin. For T7 pol, we studied insertion of natural nucleotides opposite variably sized T analogs in the template and, conversely, for variably sized dTTP analogs opposite natural template bases. The enzyme displayed extremely high selectivity for a specific base pair size, with drops in efficiency of as much as 280-fold for increases of 0.4 A beyond an optimum size approximating the size of a natural pair. The enzyme also strongly rejected pairs that were smaller than the optimum by as little as 0.3 A. The size preferences with T7 DNA pol were generally smaller, and the steric rejection was greater than DNA pol I Klenow fragment, correlating with the higher fidelity of the former. The hypothetical effects of varied active site size and rigidity are discussed. The data lend direct support to the concept that active site tightness is a chief determinant of high fidelity of replicative polymerases and that a less rigid (looser) and larger active site can lead to lower fidelity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriophage T7 / enzymology*
  • Base Pairing
  • Binding Sites
  • DNA / chemistry
  • DNA Polymerase I / chemistry
  • DNA-Directed DNA Polymerase / chemistry*
  • Escherichia coli / metabolism
  • Genetic Techniques
  • Kinetics
  • Models, Chemical
  • Oligonucleotides / chemistry
  • Protein Binding
  • Templates, Genetic
  • Thymidine / chemistry


  • Oligonucleotides
  • DNA
  • DNA Polymerase I
  • DNA-Directed DNA Polymerase
  • Thymidine