A polymer, random walk model for the size-distribution of large DNA fragments after high linear energy transfer radiation

Abstract DNA double-strand breaks (DSBs) produced by densely ionizing radiation are not located randomly in the genome: recent data indicate DSB clustering along chromosomes. Stochastic DSB clustering at large scales, from >100 Mbp down to <0.01 Mbp, is modeled using computer simulations and analytic equations. A random-walk, coarse-grained polymer model for chromatin is combined with a simple track structure model in Monte Carlo software called DNAbreak and is applied to data on alpha-particle irradiation of V-79 cells. The chromatin model neglects molecular details but systematically incorporates an increase in average spatial separation between two DNA loci as the number of base-pairs between the loci increases. Fragment-size distributions obtained using DNAbreak match data on large fragments about as well as distributions previously obtained with a less mechanistic approach. Dose-response relations, linear at small doses of high linear energy transfer (LET) radiation, are obtained. They are found to be non-linear when the dose becomes so large that there is a significant probability of overlapping or close juxtaposition, along one chromosome, for different DSB clusters from different tracks. The non-linearity is more evident for large fragments than for small. The DNAbreak results furnish an example of the RLC (randomly located clusters) analytic formalism, which generalizes the broken-stick fragment-size distribution of the random-breakage model that is often applied to low-LET data.

[1]  D T Goodhead,et al.  Track structure in radiation biology: theory and applications. , 1998, International journal of radiation biology.

[2]  D J Brenner,et al.  Constraints on energy deposition and target size of multiply damaged sites associated with DNA double-strand breaks. , 1992, International journal of radiation biology.

[3]  K. Prise,et al.  DNA double-strand break distributions in X-ray and alpha-particle irradiated V79 cells: evidence for non-random breakage. , 1997, International journal of radiation biology.

[4]  W Friedland,et al.  Simulation of DNA fragment distributions after irradiation with photons , 1999, Radiation and environmental biophysics.

[5]  G van den Engh,et al.  A random-walk/giant-loop model for interphase chromosomes. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[6]  V. Michalik Energy deposition clusters in nanometer regions of charged-particle tracks. , 1993, Radiation research.

[7]  G. Weiss Aspects and Applications of the Random Walk , 1994 .

[8]  M. Löbrich,et al.  DNA double-strand breaks induced by high-energy neon and iron ions in human fibroblasts. I. Pulsed-field gel electrophoresis method. , 1994, Radiation research.

[9]  H. Schaefer,et al.  Microdosimetric structure of heavy ion tracks in tissue , 1976, Radiation and environmental biophysics.

[10]  J. Ostashevsky A polymer model for the structural organization of chromatin loops and minibands in interphase chromosomes. , 1998, Molecular biology of the cell.

[11]  D J Brenner,et al.  Track structure, lesion development, and cell survival. , 1990, Radiation research.

[12]  C Cremer,et al.  Role of chromosome territories in the functional compartmentalization of the cell nucleus. , 1993, Cold Spring Harbor symposia on quantitative biology.

[13]  A. Friedl,et al.  An electrophoretic approach to the assessment of the spatial distribution of DNA double‐strand breaks in mammalian cells , 1995, Electrophoresis.

[14]  K. Binder Monte Carlo and molecular dynamics simulations in polymer science , 1995 .

[15]  S. Chandrasekhar Stochastic problems in Physics and Astronomy , 1943 .

[16]  J. Strouboulis,et al.  Functional compartmentalization of the nucleus. , 1996, Journal of cell science.

[17]  A. Kellerer Fundamentals of microdosimetry , 1985 .

[18]  D. Agard,et al.  Perturbation of Nuclear Architecture by Long-Distance Chromosome Interactions , 1996, Cell.

[19]  B. Stenerlöw,et al.  DNA damage induced by radiation of different linear energy transfer: initial fragmentation. , 2000, International journal of radiation biology.

[20]  J. Sedat,et al.  Deconstructing the nucleus: global architecture from local interactions. , 1997, Current opinion in genetics & development.

[21]  Aloke Chatterjee,et al.  Clusters of DNA Damage Induced by Ionizing Radiation: Formation of Short DNA Fragments. I. Theoretical Modeling , 1996 .

[22]  V. Moiseenko,et al.  Modelling the kinetics of chromosome exchange formation in human cells exposed to ionising radiation , 1996, Radiation and environmental biophysics.

[23]  A. Friedl,et al.  Computer simulation of pulsed field gel runs allows the quantitation of radiation‐induced double‐strand breaks in yeast , 1994, Electrophoresis.

[24]  R Eils,et al.  Compartmentalization of interphase chromosomes observed in simulation and experiment. , 1999, Journal of molecular biology.

[25]  R. Sachs,et al.  Radiation-induced total-deletion mutations in the human hprt gene: a biophysical model based on random walk interphase chromatin geometry. , 1998, International journal of radiation biology.

[26]  I. G. MacKenzie,et al.  Stochastic Processes with Applications , 1992 .

[27]  J. Hearst,et al.  STATISTICAL MECHANICS OF THE EXTENSIBLE AND SHEARABLE ELASTIC ROD AND OF DNA , 1996 .

[28]  B. Rydberg,et al.  Clusters of DNA damage induced by ionizing radiation: formation of short DNA fragments. II. Experimental detection. , 1996, Radiation research.

[29]  M. Löbrich,et al.  Non-random distribution of DNA double-strand breaks induced by particle irradiation. , 1996, International journal of radiation biology.

[30]  A. Chatterjee,et al.  Energy deposition mechanisms and biochemical aspects of DNA strand breaks by ionizing radiation , 1991 .

[31]  C S Lange,et al.  The 30 nm chromatin fiber as a flexible polymer. , 1994, Journal of biomolecular structure & dynamics.

[32]  Rainer K. Sachs,et al.  Polymer chromosome models and Monte Carlo simulations of radiation breaking DNA , 1999, Bioinform..

[33]  A Ottolenghi,et al.  DNA complex lesions induced by protons and ⋅-particles: track structure characteristics determining linear energy transfer and particle type dependence , 1997, Radiation and environmental biophysics.

[34]  R K Sachs,et al.  Locations of radiation-produced DNA double strand breaks along chromosomes: a stochastic cluster process formalism. , 1999, Mathematical biosciences.

[35]  W. Dewey,et al.  Methods for the quantification of DNA double-strand breaks determined from the distribution of DNA fragment sizes measured by pulsed-field gel electrophoresis. , 1995, Radiation research.

[36]  H. Paretzke,et al.  Monte Carlo simulation of the production of short DNA fragments by low-linear energy transfer radiation using higher-order DNA models. , 1998, Radiation research.

[37]  K. Weber,et al.  DNA double-strand breaks in mammalian cells exposed to gamma-rays and very heavy ions. Fragment-size distributions determined by pulsed-field gel electrophoresis. , 1998, Radiation and environmental biophysics.

[38]  P. Gennes Scaling Concepts in Polymer Physics , 1979 .

[39]  Kurt Binder,et al.  Modeling polyethylene with the bond fluctuation model , 1997 .

[40]  D. Brenner,et al.  A formalism for analysing large-scale clustering of radiation-induced breaks along chromosomes. , 1998, International journal of radiation biology.

[41]  A. Chatterjee,et al.  Clusters of DNA induced by ionizing radiation: formation of short DNA fragments. I. Theoretical modeling. , 1996, Radiation research.

[42]  M. Flentje,et al.  DNA double-strand breaks in mammalian cells exposed to Á-rays and very heavy ions , 1998 .