TY - JOUR
T1 - Dpo4 is hindered in extending a G·T mismatch by a reverse wobble
AU - Trincao, Jose
AU - Johnson, Robert E.
AU - Wolfle, William T.
AU - Escalante, Carlos R.
AU - Prakash, Satya
AU - Prakash, Louise
AU - Aggarwal, Aneel K.
N1 - Funding Information:
We thank the staff at the Advanced Photon Source and the National Synchrotron Light Source for facilitating X-ray data collection. We thank T. Edwards for help with data collection and processing. This was supported was supported by US National Institutes of Health grant CA094006 (A.K.A. and L.P.).
PY - 2004/5
Y1 - 2004/5
N2 - 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.
AB - 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.
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U2 - 10.1038/nsmb755
DO - 10.1038/nsmb755
M3 - Article
C2 - 15077104
AN - SCOPUS:2342644853
SN - 1545-9993
VL - 11
SP - 457
EP - 462
JO - Nature Structural and Molecular Biology
JF - Nature Structural and Molecular Biology
IS - 5
ER -