Dpo4 is hindered in extending a G.T mismatch by a reverse wobble.
Nature structural & molecular biology (2004), Volume 11, Page 457
Abstract:
The ability or inability of a DNA polymerase to extend a mispair directly affects the establishment of genomic mutations. We report here kinetic analyses of the ability of Dpo4, a Y-family polymerase from Sulfolobus solfataricus, to extend from all mispairs opposite a template G or T. Dpo4 is equally inefficient at extending these mispairs, which include, surprisingly, a G.T mispair expected to conform closely to Watson-Crick geometry. To elucidate the basis of this, we solved the structure of Dpo4 bound to G.T-mispaired primer template in the presence of an incoming nucleotide. As a control, we also determined the structure of Dpo4 bound to a matched A-T base pair at the primer terminus. The structures offer a basis for the low efficiency of Dpo4 in extending a G.T mispair: a reverse wobble that deflects the primer 3'-OH away from the incoming nucleotide.
Polymerases:
Topics:
Other Enzymatic Activities, Structure and Structure/Function, Fidelity
Status:
new | topics/pols set | partial results | complete | validated |
Results:
No results available for this paper.