Literature DB >> 35744

Single-strand breaks in DNA during repair of UV-induced damage in normal human and xeroderma pigmentosum cells as determined by alkaline DNA unwinding and hydroxylapatite chromatography: effects of hydroxyurea, 5-fluorodeoxyuridine and 1-beta-D-arabinofuranosylcytosine on the kinetics of repair.

K Erixon, G Ahnström.   

Abstract

A simple and sensitive technique for detection of strand breaks in DNA has been further developed. The method has been used to follow UV-induced excision-repair in human fibroblasts. It has been possible to study the kinetics of enzymic reactions in intact cells, in which strand breaks in DNA are produced and sealed again. Hydroxyurea, 5-fluorodeoxyuridine and 1-beta-D-arabinofuranosylcytosine, potent inhibitors of DNA synthesis, drastically increased the number of breaks observed during the repair process. This was probably due to a decreased polymerase activity, which will cause the strand breaks formed by endonuclease to remain open longer. The initial rate of strand-break formation did not seem to be influenced by hydroxyurea or araC, and was about 4000 breaks per minute in a diploid genome, at a dose of 20 J/m2. After 5--30 min, depending on the dose of UV, the number of breaks reached a maximum and started to decrease again. Hydroxyurea decreased the rate of polymerization in the sites under repair. However, there was no concomitant reduction of repair-induced incorporation of [3H]thymidine and no reduction of the excision of pyrimidine dimers. It therefore seems that the action of the polymerase was not a rate-limiting event, but rather an earlier step. It is likely that the endonucleolytic activity determined the rate of repair. As a consequence, the endonuclease and polymerase cannot be bound in a permanent complex. Under certain assumptions, the time for repair of a site, i.e. the time from incision to final ligase sealing, can be estimated as between 3 and 10 min. Essentially no breaks were produced in Xeroderma pigmentosum cells belonging to complementation group A, and there was no enhancement by hydroxyurea. Cells from the variant type of Xeroderma pigmentosum behaved like normal cells in this respect.

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Year:  1979        PMID: 35744     DOI: 10.1016/0027-5107(79)90164-7

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  38 in total

1.  Replication factor C recruits DNA polymerase delta to sites of nucleotide excision repair but is not required for PCNA recruitment.

Authors:  René M Overmeer; Audrey M Gourdin; Ambra Giglia-Mari; Hanneke Kool; Adriaan B Houtsmuller; Gregg Siegal; Maria I Fousteri; Leon H F Mullenders; Wim Vermeulen
Journal:  Mol Cell Biol       Date:  2010-08-16       Impact factor: 4.272

2.  H2AX phosphorylation within the G1 phase after UV irradiation depends on nucleotide excision repair and not DNA double-strand breaks.

Authors:  Thomas M Marti; Eli Hefner; Luzviminda Feeney; Valerie Natale; James E Cleaver
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-20       Impact factor: 11.205

Review 3.  The identification of translesion DNA synthesis regulators: Inhibitors in the spotlight.

Authors:  A P Bertolin; S F Mansilla; V Gottifredi
Journal:  DNA Repair (Amst)       Date:  2015-05-12

Review 4.  A comparison of the effects of cytosine arabinoside and beta-lactams on DNA synthesis and cellular proliferation.

Authors:  R J Fram
Journal:  Cell Biol Toxicol       Date:  1986-12       Impact factor: 6.691

5.  Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells.

Authors:  J E Arrand; N M Bone; R T Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

6.  The effects of inhibitors of topoisomerase II and quinacrine on ultraviolet-light-induced DNA incision in normal and xeroderma pigmentosum fibroblasts.

Authors:  H W Thielmann; O Popanda; L Edler
Journal:  J Cancer Res Clin Oncol       Date:  1991       Impact factor: 4.553

7.  Mammalian ribonucleotide reductase subunit p53R2 is required for mitochondrial DNA replication and DNA repair in quiescent cells.

Authors:  Giovanna Pontarin; Paola Ferraro; Leonardo Bee; Peter Reichard; Vera Bianchi
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-30       Impact factor: 11.205

8.  The effect of hydroxyurea on the expression of the common fragile site at 3p14.

Authors:  Z A Yan; X Z Li; X T Zhou
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

9.  Application of arabinofuranosyl cytosine in the kinetic analysis and quantitation of DNA repair in human cells after ultraviolet irradiation.

Authors:  R D Snyder; W L Carrier; J D Regan
Journal:  Biophys J       Date:  1981-08       Impact factor: 4.033

10.  The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links.

Authors:  Ali Z Al-Minawi; Yin-Fai Lee; Daniel Håkansson; Fredrik Johansson; Cecilia Lundin; Nasrollah Saleh-Gohari; Niklas Schultz; Dag Jenssen; Helen E Bryant; Mark Meuth; John M Hinz; Thomas Helleday
Journal:  Nucleic Acids Res       Date:  2009-08-27       Impact factor: 16.971

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