Literature DB >> 467424

DNA polymerase beta from brain neurons is a repair enzyme.

J Waser, U Hübscher, C C Kuenzle, S Spadari.   

Abstract

DNA polymerase beta was isolated from rat cortex neurons and characterised. Its properties were strikingly similar to those of other mammalian beta-polymerases. In adult rats, this was the major DNA polymerase occurring in neuronal nuclei, which contained no alpha-polymerase, 99.2% beta-polymerase and only 0.8% gamma-polymerase. Isolated neuronal nuclei of this developmental stage were shown to perform ultraviolet-induced repair DNA synthesis in vitro. Since beta-polymerase was virtually the exclusive DNA polymerase in these nuclei it was concluded that the beta enzyme was responsible for the observed DNA repair. This was further substantiated by demonstrating a virtually complete suppression of DNA repair in irradiated nuclei by 2',3'-dideoxyribosylthymine 5'-triphosphate (d2TTP), a potent beta-polymerase inhibitor. However, the presence of minute amounts of gamma-polymerase in neuronal nuclei and its susceptibility to d2TTP did not allow one to rule out an ancillary role of DNA polymerase gamma in DNA repair. In view of the similarity of the neuronal DNA polymerase beta with all other mammalian beta-polymerases it may be speculated that the ability to perform repair DNA synthesis is not unique to the neuronal enzyme but is a general function of all beta-polymerases.

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Year:  1979        PMID: 467424     DOI: 10.1111/j.1432-1033.1979.tb13122.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  28 in total

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2.  Betalactam antibiotics interfere with eukaryotic DNA-replication by inhibiting DNA polymerase alpha.

Authors:  U H Do; K A Neftel; S Spadari; U Hübscher
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3.  DNA polymerase beta null mouse embryonic fibroblasts harbor a homozygous null mutation in DNA polymerase iota.

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Journal:  DNA Repair (Amst)       Date:  2006-09-18

Review 4.  DNA damage and repair: relevance to mechanisms of neurodegeneration.

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Review 5.  Brain capacity for repair of oxidatively damaged DNA and preservation of neuronal function.

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6.  The specific binding of nuclear protein(s) to the cAMP responsive element (CRE) sequence (TGACGTCA) is reduced by the misincorporation of U and increased by the deamination of C.

Authors:  A Verri; P Mazzarello; G Biamonti; S Spadari; F Focher
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

7.  DNA replication and postreplication mismatch repair in cell-free extracts from cultured human neuroblastoma and fibroblast cells.

Authors:  P David; E Efrati; G Tocco; S W Krauss; M F Goodman
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8.  Effects of beta-lactams on DNA replication.

Authors:  U Hübscher; U D Huynh; M Hässig; K A Neftel
Journal:  Cell Biol Toxicol       Date:  1986-12       Impact factor: 6.691

9.  Unscheduled DNA synthesis in various types of cells of the mouse brain in vivo.

Authors:  H Korr; B Schultze
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

10.  Hepatitis-B virus-associated deoxyribonucleic acid polymerase: a partial characterization by the use of chemical agents.

Authors:  G Hess; W Arnold; K H Meyer zum Büschenfelde
Journal:  Klin Wochenschr       Date:  1981-06-15
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