A Computational Approach to the Relationship between Radiation Induced Double Strand Breaks and Translocations

1994 ◽  
pp. 251-259
Author(s):  
William R. Holley ◽  
Aloke Chatterjee
Keyword(s):  
Computational Approach ◽  
Double Strand Breaks ◽  
Strand Breaks ◽  
Radiation Induced ◽  
The Relationship

Role for Artemis nuclease in the repair of radiation-induced DNA double strand breaks by alternative end joining

DNA Repair ◽  
2015 ◽  
Vol 31 ◽  
pp. 29-40 ◽  
Author(s):  
Mario Moscariello ◽  
Radi Wieloch ◽  
Aya Kurosawa ◽  
Fanghua Li ◽  
Noritaka Adachi ◽  
...  
Keyword(s):  
Double Strand Breaks ◽  
Dna Double Strand Breaks ◽  
End Joining ◽  
Strand Breaks ◽  
Alternative End Joining ◽  
Radiation Induced

scholarly journals Double-strand DNA breaks recruit the centromeric histone CENP-A

2009 ◽  
Vol 106 (37) ◽  
pp. 15762-15767 ◽  
Author(s):  
Samantha G. Zeitlin ◽  
Norman M. Baker ◽  
Brian R. Chapados ◽  
Evi Soutoglou ◽  
Jean Y. J. Wang ◽  
...  
Keyword(s):  
Dna Cleavage ◽  
Strand Break ◽  
Double Strand Breaks ◽  
Dna Breaks ◽  
End Joining ◽  
Strand Breaks ◽  
Double Strand Dna Breaks ◽  
Histone H3 Variant ◽  
Radiation Induced ◽  
Non Homologous End Joining

The histone H3 variant CENP-A is required for epigenetic specification of centromere identity through a loading mechanism independent of DNA sequence. Using multiphoton absorption and DNA cleavage at unique sites by I-SceI endonuclease, we demonstrate that CENP-A is rapidly recruited to double-strand breaks in DNA, along with three components (CENP-N, CENP-T, and CENP-U) associated with CENP-A at centromeres. The centromere-targeting domain of CENP-A is both necessary and sufficient for recruitment to double-strand breaks. CENP-A accumulation at DNA breaks is enhanced by active non-homologous end-joining but does not require DNA-PKcs or Ligase IV, and is independent of H2AX. Thus, induction of a double-strand break is sufficient to recruit CENP-A in human and mouse cells. Finally, since cell survival after radiation-induced DNA damage correlates with CENP-A expression level, we propose that CENP-A may have a function in DNA repair.

scholarly journals SIMULATION AND SENSITIVITY ANALYSIS ON THE PARAMETER OF NON-TARGETED IRRADIATION EFFECTS MODEL

2018 ◽  
Vol 81 (1) ◽  
Author(s):  
Muhamad Hanis Nasir ◽  
Fuaada Mohd Siam
Keyword(s):  
Mathematical Model ◽  
Sensitivity Analysis ◽  
Real Life ◽  
Double Strand Breaks ◽  
Signal Molecules ◽  
Danger Signal ◽  
Survival Fraction ◽  
Strand Breaks ◽  
Radiation Induced ◽  
The Mathematical Model

Real-life situations showed damage effects on non-targeted cells located in the vicinity of an irradiation region, due to danger signal molecules released by the targeted cells. This effect is widely known as radiation-induced bystander effects (RIBE). The purpose of this paper is to model the interaction of non-targeted cells towards bystander factors released by the irradiated cells by using a system of structured ordinary differential equations. The mathematical model and its simulations are presented in this paper. In the model, the cells are grouped based on the number of double-strand breaks (DSBs) and mis-repair DSBs because the DSBs are formed in non-targeted cells. After performing the model's simulations, the analysis continued with sensitivity analysis. Sensitivity analysis will determine which parameter in the model is the most sensitive to the survival fraction of non-targeted cells. The proposed mathematical model can explain the survival fraction of non-targeted cells affected by the bystander factors.

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