Literature DB >> 18366182

Biochemical evolution of DNA polymerase eta: properties of plant, human, and yeast proteins.

Peter D Hoffman1, Marc J Curtis, Shigenori Iwai, John B Hays.   

Abstract

To assess how evolution might have biochemically shaped DNA polymerase eta (Poleta) in plants, we expressed in Escherichia coli proteins from Arabidopsis thaliana (At), humans (Hs), and the yeast Saccharomyces cerevisiae (Sc), purified them to near homogeneity, and compared their properties. Consistent with the multiple divergent amino acids within mostly conserved polymerase domains, the polymerases showed modest, appreciable, and marked differences, respectively, in salt and temperature optima for activity and thermostability. We compared abilities to extend synthetic primers past template cyclobutane thymine dimers (T[CPD]T) or undamaged T-T under physiological conditions (80-110 mM salt). Specific activities for "standing-start" extension of synthetic primers ending opposite the second template nucleotide 3' to T-T were roughly similar. During subsequent "running-start" insertions past T-T and the next 5' ( N + 1) nucleotide, AtPoleta and HsPoleta appeared more processive, but DNA sequence contexts strongly affected termination probabilities. Lesion-bypass studies employed four different templates containing T[CPD]Ts, and two containing pyrimidine (6-4')-pyrimidinone photoproducts ([6-4]s). AtPoleta made the three successive insertions [opposite the T[CPD]T and (N + 1) nucleotides] that define bypass nearly as well as HsPoleta and somewhat better than ScPoleta. Again, sequence context effects were profound. Interestingly, the level of insertion opposite the ( N - 1) nucleotide 3' to T[CPD]T by HsPoleta and especially AtPoleta, but not ScPoleta, was reduced (up to 4-fold) relative to the level of insertion opposite the ( N - 1) nucleotide 3' to T-T. Evolutionary conservation of efficient T[CPD]T bypass by HsPoleta and AtPoleta may reflect a high degree of exposure of human skin and plants to solar UV-B radiation. The depressed ( N - 1) insertion upstream of T[CPD]T (but not T-T) may reduce the extent of gratuitous error-prone insertion.

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Year:  2008        PMID: 18366182     DOI: 10.1021/bi701781p

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  6 in total

1.  Role of AtPolζ, AtRev1, and AtPolη in UV light-induced mutagenesis in Arabidopsis.

Authors:  Mayu Nakagawa; Shinya Takahashi; Atsushi Tanaka; Issay Narumi; Ayako N Sakamoto
Journal:  Plant Physiol       Date:  2010-10-28       Impact factor: 8.340

2.  Characterization of a Y-Family DNA Polymerase eta from the Eukaryotic Thermophile Alvinella pompejana.

Authors:  Sayo Kashiwagi; Isao Kuraoka; Yoshie Fujiwara; Kenichi Hitomi; Quen J Cheng; Jill O Fuss; David S Shin; Chikahide Masutani; John A Tainer; Fumio Hanaoka; Shigenori Iwai
Journal:  J Nucleic Acids       Date:  2010-09-20

3.  Phosphorylation regulates human polη stability and damage bypass throughout the cell cycle.

Authors:  Federica Bertoletti; Valentina Cea; Chih-Chao Liang; Taiba Lanati; Antonio Maffia; Mario D M Avarello; Lina Cipolla; Alan R Lehmann; Martin A Cohn; Simone Sabbioneda
Journal:  Nucleic Acids Res       Date:  2017-09-19       Impact factor: 16.971

Review 4.  Translesion Synthesis in Plants: Ultraviolet Resistance and Beyond.

Authors:  Ayako N Sakamoto
Journal:  Front Plant Sci       Date:  2019-10-09       Impact factor: 5.753

Review 5.  The Dark Side of UV-Induced DNA Lesion Repair.

Authors:  Wojciech Strzałka; Piotr Zgłobicki; Ewa Kowalska; Aneta Bażant; Dariusz Dziga; Agnieszka Katarzyna Banaś
Journal:  Genes (Basel)       Date:  2020-12-02       Impact factor: 4.096

6.  Correlations in Somatic Hypermutation Between Sites in IGHV Genes Can Be Explained by Interactions Between AID and/or Polη Hotspots.

Authors:  Artem Krantsevich; Catherine Tang; Thomas MacCarthy
Journal:  Front Immunol       Date:  2021-02-02       Impact factor: 7.561

  6 in total

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