Accuracy of thymine–thymine dimer bypass by Saccharomyces cerevisiae DNA polymerase η
Author(s) -
M. Todd Washington,
R. E. Johnson,
Satya Prakash,
Louise Prakash
Publication year - 2000
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.97.7.3094
Subject(s) - dna polymerase , thymine , pyrimidine dimer , dna polymerase ii , saccharomyces cerevisiae , dna , dna clamp , dna replication , base pair , dimer , polymerase , biology , processivity , dna polymerase mu , dna polymerase delta , stereochemistry , biochemistry , microbiology and biotechnology , chemistry , yeast , dna repair , gene , polymerase chain reaction , circular bacterial chromosome , reverse transcriptase , organic chemistry
TheSaccharomyces cerevisiae RAD30 gene functions in error-free replication of UV-damaged DNA.RAD30 encodes a DNA polymerase, Pol η, which inserts two adenines opposite the two thymines of acis -syn thymine–thymine (T–T) dimer. Here we use steady-state kinetics to determine the accuracy of DNA synthesis opposite the T–T dimer. Surprisingly, the accuracy of DNA synthesis opposite the damaged DNA is nearly indistinguishable from that opposite nondamaged DNA, with frequencies of misincorporation of about 10−2 to 10−3 . These studies support the hypothesis that unlike most DNA polymerases, Pol η is able to tolerate distortions in DNA resulting from damage, which then enables the polymerase to utilize the intrinsic base pairing ability of the T–T dimer.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom