TY - JOUR
T1 - Fidelity and processivity of DNA synthesis by DNA polymerase κ, the product of the human DINB1 gene
AU - Ohashi, Eiji
AU - Bebenek, Katarzyna
AU - Matsuda, Toshiro
AU - Feaver, William J.
AU - Gerlach, Valerie L.
AU - Friedberg, Errol C.
AU - Ohmori, Haruo
AU - Kunkel, Thomas A.
PY - 2000/12/15
Y1 - 2000/12/15
N2 - Mammalian DNA polymerase κ (pol κ), a member of the UmuC/DinB nucleotidyl transferase superfamily, has been implicated in spontaneous mutagenesis. Here we show that human pol κ copies undamaged DNA with average single-base substitution and deletion error rates of 7 × 10-3 and 2 × 10-3, respectively. These error rates are high when compared to those of most other DNA polymerases, pol κ also has unusual error specificity, producing a high proportion of T·CMP mispairs and deleting and adding non-reiterated nucleotides at extraordinary rates. Unlike other members of the UmuC/ DinB family, pol κ can processively synthesize chains of 25 or more nucleotides. This moderate processivity may reflect a contribution of C-terminal residues, which include two zinc clusters. The very low fidelity and moderate processivity of pol κ is novel in comparison to any previously studied DNA polymerase, and is consistent with a role in spontaneous mutagenesis.
AB - Mammalian DNA polymerase κ (pol κ), a member of the UmuC/DinB nucleotidyl transferase superfamily, has been implicated in spontaneous mutagenesis. Here we show that human pol κ copies undamaged DNA with average single-base substitution and deletion error rates of 7 × 10-3 and 2 × 10-3, respectively. These error rates are high when compared to those of most other DNA polymerases, pol κ also has unusual error specificity, producing a high proportion of T·CMP mispairs and deleting and adding non-reiterated nucleotides at extraordinary rates. Unlike other members of the UmuC/ DinB family, pol κ can processively synthesize chains of 25 or more nucleotides. This moderate processivity may reflect a contribution of C-terminal residues, which include two zinc clusters. The very low fidelity and moderate processivity of pol κ is novel in comparison to any previously studied DNA polymerase, and is consistent with a role in spontaneous mutagenesis.
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U2 - 10.1074/jbc.M005309200
DO - 10.1074/jbc.M005309200
M3 - Article
C2 - 11006276
AN - SCOPUS:0034671730
SN - 0021-9258
VL - 275
SP - 39678
EP - 39684
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 50
ER -