TY - JOUR
T1 - The fidelity of DNA synthesis by yeast DNA polymerase zeta alone and with accessory proteins
AU - Zhong, Xuejun
AU - Garg, Parie
AU - Stith, Carrie M.
AU - McElhinny, Stephanie A.Nick
AU - Kissling, Grace E.
AU - Burgers, Peter M.J.
AU - Kunkel, Thomas A.
PY - 2006/10
Y1 - 2006/10
N2 - DNA polymerase zeta (pol ζ) participates in several DNA transactions in eukaryotic cells that increase spontaneous and damage-induced mutagenesis. To better understand this central role in mutagenesis in vivo, here we report the fidelity of DNA synthesis in vitro by yeast pol ζ alone and with RFC, PCNA and RPA. Overall, the accessory proteins have little effect on the fidelity of pol ζ. Pol ζ is relatively accurate for single base insertion/deletion errors. However, the average base substitution fidelity of pol ζ is substantially lower than that of homologous B family pols α, δ and ε. Pol ζ is particularly error prone for substitutions in specific sequence contexts and generates multiple single base errors clustered in short patches at a rate that is unprecedented in comparison with other polymerases. The unique error specificity of pol ζ in vitro is consistent with Pol ζ-dependent mutagenic specificity reported in vivo. This fact, combined with the high rate of single base substitution errors and complex mutations observed here, indicates that pol ζ contributes to mutagenesis in vivo not only by extending mismatches made by other polymerases, but also by directly generating its own mismatches and then extending them.
AB - DNA polymerase zeta (pol ζ) participates in several DNA transactions in eukaryotic cells that increase spontaneous and damage-induced mutagenesis. To better understand this central role in mutagenesis in vivo, here we report the fidelity of DNA synthesis in vitro by yeast pol ζ alone and with RFC, PCNA and RPA. Overall, the accessory proteins have little effect on the fidelity of pol ζ. Pol ζ is relatively accurate for single base insertion/deletion errors. However, the average base substitution fidelity of pol ζ is substantially lower than that of homologous B family pols α, δ and ε. Pol ζ is particularly error prone for substitutions in specific sequence contexts and generates multiple single base errors clustered in short patches at a rate that is unprecedented in comparison with other polymerases. The unique error specificity of pol ζ in vitro is consistent with Pol ζ-dependent mutagenic specificity reported in vivo. This fact, combined with the high rate of single base substitution errors and complex mutations observed here, indicates that pol ζ contributes to mutagenesis in vivo not only by extending mismatches made by other polymerases, but also by directly generating its own mismatches and then extending them.
UR - http://www.scopus.com/inward/record.url?scp=33748941448&partnerID=8YFLogxK
U2 - 10.1093/nar/gkl465
DO - 10.1093/nar/gkl465
M3 - Article
C2 - 16971464
AN - SCOPUS:33748941448
SN - 0305-1048
VL - 34
SP - 4731
EP - 4742
JO - Nucleic acids research
JF - Nucleic acids research
IS - 17
ER -