Literature DB >> 9728743

DNA double-strand breaks in mammalian cells exposed to gamma-rays and very heavy ions. Fragment-size distributions determined by pulsed-field gel electrophoresis.

F Kraxenberger1, K J Weber, A A Friedl, F Eckardt-Schupp, M Flentje, P Quicken, A M Kellerer.   

Abstract

The spatial distribution of DNA double-strand breaks (DSB) was assessed after treatment of mammalian cells (V79) with densely ionizing radiation. Cells were exposed to beams of heavy charged particles (calcium ions: 6.9 MeV/u, 2.1.10(3) keV/microm; uranium ions: 9.0 MeV/u, 1.4.10(4) keV/microm) at the linear accelerator UNILAC of GSI, Darmstadt. DNA was isolated in agarose plugs and subjected to pulsed-field gel electrophoresis under conditions that separated DNA fragments of size 50 kbp to 5 Mbp. The measured fragment distributions were compared to those obtained after gamma-irradiation and were analyzed by means of a convolution and a deconvolution technique. In contrast to the finding for gamma-radiation, the distributions produced by heavy ions do not correspond to the random breakage model. Their marked overdispersion and the observed excess of short fragments reflect spatial clustering of DSB that extends over large regions of the DNA, up to several mega base pairs (Mbp). At fluences of 0.75 and 1.5/microm2, calcium ions produce nearly the same shape of fragment spectrum, merely with a difference in the amount of DNA entering the gel; this suggests that the DNA is fragmented by individual calcium ions. At a fluence of 0.8/microm2 uranium ions produce a profile that is shifted to smaller fragment sizes in comparison to the profile obtained at a fluence of 0.4/microm2; this suggests cumulative action of two separate ions in the formation of fragments. These observations are not consistent with the expectation that the uranium ions, with their much larger LET, should be more likely to produce single particle action than the calcium ions. However, a consideration of the greater lateral extension of the tracks of the faster uranium ions explains the observed differences; it suggests that the DNA is closely coiled so that even DNA locations several Mbp apart are usually not separated by less than 0. 1 or 0.2 microm.

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Year:  1998        PMID: 9728743     DOI: 10.1007/s004110050102

Source DB:  PubMed          Journal:  Radiat Environ Biophys        ISSN: 0301-634X            Impact factor:   1.925


  5 in total

1.  Microirradiation of cells with energetic heavy ions.

Authors:  A Hauptner; S Dietzel; G A Drexler; P Reichart; R Krücken; T Cremer; A A Friedl; G Dollinger
Journal:  Radiat Environ Biophys       Date:  2004-01-20       Impact factor: 1.925

2.  Observation of DNA damage of human hepatoma cells irradiated by heavy ions using comet assay.

Authors:  Li-Mei Qiu; Wen-Jian Li; Xin-Yue Pang; Qing-Xiang Gao; Yan Feng; Li-Bin Zhou; Gao-Hua Zhang
Journal:  World J Gastroenterol       Date:  2003-07       Impact factor: 5.742

Review 3.  Involvement of p53 in the repair of DNA double strand breaks: multifaceted Roles of p53 in homologous recombination repair (HRR) and non-homologous end joining (NHEJ).

Authors:  Vijay Menon; Lawrence Povirk
Journal:  Subcell Biochem       Date:  2014

4.  Subtraction of background damage in PFGE experiments on DNA fragment-size distributions.

Authors:  Artem L Ponomarev; Mauro Belli; Philip J Hahnfeldt; Lynn Hlatky; Rainer K Sachs; Francis A Cucinotta
Journal:  Radiat Environ Biophys       Date:  2007-04-04       Impact factor: 2.017

5.  Short DNA Fragments Are a Hallmark of Heavy Charged-Particle Irradiation and May Underlie Their Greater Therapeutic Efficacy.

Authors:  Dalong Pang; Sergey Chasovskikh; James E Rodgers; Anatoly Dritschilo
Journal:  Front Oncol       Date:  2016-06-10       Impact factor: 6.244

  5 in total

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