Literature DB >> 3756143

Production of dihydrothymidine stereoisomers in DNA by gamma-irradiation.

E A Furlong, T J Jorgensen, W D Henner.   

Abstract

5,6-Dihydrothymidine (dDHT) is a derivative thymidine formed during gamma-irradiation. This paper demonstrates the conditions under which dDHT is formed in solutions of DNA and that dDHT is produced in the DNA of HeLa cells during gamma-irradiation. The product of dDHT by gamma-irradiation of either thymidine or DNA has been quantitated by a sensitive and specific high-pressure liquid chromatography method. dDHT is a major product of the anoxic irradiation of thymidine (G value 0.5) but is produced in substantially smaller amounts in DNA irradiated under the same conditions (G value 0.026). The presence of oxygen reduces the yield of dDHT by at least 25-fold for both irradiation substrates. In HeLa cells, 60Co irradiation under anoxia produces (6.2 +/- 0.2) X 10(-8) mol of the R isomer of dDHT per mole of cell deoxynucleotide per gray (G value 0.11). gamma-Irradiation of thymidine produces equal quantities of the R and S stereoisomers of dDHT. Irradiation of DNA produces significantly more (69%) (R)- than (S)-dDHT. DNA isolated from cultured human cells following gamma-irradiation also contains more of the R than the S form of dDHT. The conformation of double-stranded DNA favors a stereospecific production of the R isomer. Among products of gamma-irradiation of DNA, dDHT is unique in its strict requirement for anoxia during irradiation and the preferential production of a particular stereoisomer.

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Year:  1986        PMID: 3756143     DOI: 10.1021/bi00363a025

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


  5 in total

1.  Characterisation of new substrate specificities of Escherichia coli and Saccharomyces cerevisiae AP endonucleases.

Authors:  Alexander A Ishchenko; Guenhaël Sanz; Cyril V Privezentzev; Andrei V Maksimenko; Murat Saparbaev
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

2.  The major human AP endonuclease (Ape1) is involved in the nucleotide incision repair pathway.

Authors:  Laurent Gros; Alexander A Ishchenko; Hiroshi Ide; Rhoderick H Elder; Murat K Saparbaev
Journal:  Nucleic Acids Res       Date:  2004-01-02       Impact factor: 16.971

3.  Lys98 substitution in human AP endonuclease 1 affects the kinetic mechanism of enzyme action in base excision and nucleotide incision repair pathways.

Authors:  Nadezhda A Timofeyeva; Vladimir V Koval; Alexander A Ishchenko; Murat K Saparbaev; Olga S Fedorova
Journal:  PLoS One       Date:  2011-09-01       Impact factor: 3.240

4.  The roles of specific glycosylases in determining the mutagenic consequences of clustered DNA base damage.

Authors:  Naoya Shikazono; Colin Pearson; Peter O'Neill; John Thacker
Journal:  Nucleic Acids Res       Date:  2006-08-07       Impact factor: 16.971

Review 5.  Evolutionary Origins of DNA Repair Pathways: Role of Oxygen Catastrophe in the Emergence of DNA Glycosylases.

Authors:  Paulina Prorok; Inga R Grin; Bakhyt T Matkarimov; Alexander A Ishchenko; Jacques Laval; Dmitry O Zharkov; Murat Saparbaev
Journal:  Cells       Date:  2021-06-24       Impact factor: 6.600

  5 in total

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