TY - JOUR
T1 - Replication of ribonucleotide-containing DNA templates by yeast replicative polymerases
AU - Watt, Danielle L.
AU - Johansson, Erik
AU - Burgers, Peter M.
AU - Kunkel, Thomas A.
N1 - Funding Information:
We thank Katarzyna Bebenek and Jessica Williams for helpful comments on the manuscript, Amy Abdulovic for providing purified Pol δ holoenzyme, and Else-Britt Lundström for providing purified Pol ϵ enzymes. This work was supported by Project Z01 ES065070 to T.A.K. from the Division of Intramural Research of the NIH, NIEHS, by the Swedish Research Council, the Swedish Cancer Society, Smärtafonden and the fund for Basic Science-oriented Biotechnology, Medical Faculty of Umeå University to E.J., and by NIH grant GM032431 to P.M.B.
PY - 2011/8/15
Y1 - 2011/8/15
N2 - The major replicative DNA polymerases of S. cerevisiae (Pols α, δ, and e{open}) incorporate substantial numbers of ribonucleotides into DNA during DNA synthesis. When these ribonucleotides are not removed in vivo, they reside in the template strand used for the next round of replication and could potentially reduce replication efficiency and fidelity. To examine if the presence of ribonucleotides in a DNA template impede DNA synthesis, we determined the efficiency with which Pols α, δ, and e{open} copy DNA templates containing a single ribonucleotide. All three polymerases can replicate past ribonucleotides. Relative to all-DNA templates, bypass of ribo-containing templates is slightly reduced, to extents that depend on the identity of the ribo and the sequence context in which it resides. Bypass efficiencies for Pols δ and e{open} were increased by increasing the dNTP concentrations to those induced by cellular stress, and in the case of Pol e{open}, by inactivating the 3′-exonuclease activity. Overall, ribonucleotide bypass efficiencies are comparable to, and usually exceed, those for the common oxidative stress-induced lesion 8-oxo-guanine.
AB - The major replicative DNA polymerases of S. cerevisiae (Pols α, δ, and e{open}) incorporate substantial numbers of ribonucleotides into DNA during DNA synthesis. When these ribonucleotides are not removed in vivo, they reside in the template strand used for the next round of replication and could potentially reduce replication efficiency and fidelity. To examine if the presence of ribonucleotides in a DNA template impede DNA synthesis, we determined the efficiency with which Pols α, δ, and e{open} copy DNA templates containing a single ribonucleotide. All three polymerases can replicate past ribonucleotides. Relative to all-DNA templates, bypass of ribo-containing templates is slightly reduced, to extents that depend on the identity of the ribo and the sequence context in which it resides. Bypass efficiencies for Pols δ and e{open} were increased by increasing the dNTP concentrations to those induced by cellular stress, and in the case of Pol e{open}, by inactivating the 3′-exonuclease activity. Overall, ribonucleotide bypass efficiencies are comparable to, and usually exceed, those for the common oxidative stress-induced lesion 8-oxo-guanine.
KW - DNA replication
KW - RNMP bypass
KW - Ribonucleotides
KW - Translesion synthesis
UR - http://www.scopus.com/inward/record.url?scp=79960698210&partnerID=8YFLogxK
U2 - 10.1016/j.dnarep.2011.05.009
DO - 10.1016/j.dnarep.2011.05.009
M3 - Article
C2 - 21703943
AN - SCOPUS:79960698210
VL - 10
SP - 897
EP - 902
JO - DNA Repair
JF - DNA Repair
SN - 1568-7864
IS - 8
ER -