Biological Effectiveness of Accelerated Protons for Chromosome Exchanges.
Kerry A George1, Megumi Hada1, Francis A Cucinotta2
1Wyle Science, Technology and Engineering Group , Houston, TX , USA.
Frontiers in Oncology
|November 6, 2015
Summary
Proton radiation at various energies induces chromosome exchanges in human cells. Higher complex exchanges were observed compared to gamma rays, impacting space radiation protection and proton therapy strategies.
Area of Science:
- Radiation biology
- Human cell research
- Genetics
Background:
- Understanding the biological effects of proton radiation is crucial for radiation protection and therapy.
- Chromosome aberrations are key indicators of radiation-induced DNA damage.
Purpose of the Study:
- To investigate chromosome exchanges induced by protons of varying energies (5-2500 MeV) in human lymphocytes.
- To determine the relative biological effectiveness (RBE) of these proton beams.
- To assess the impact of shielding on proton-induced DNA damage.
Main Methods:
- Human lymphocytes were irradiated in vitro with seven proton energies.
- Chromosome damage was analyzed using three-color fluorescence in situ hybridization (FISH) chromosome painting.
- Relative biological effectiveness (RBE) was calculated relative to gamma rays.
Main Results:
- All proton energies induced a higher percentage of complex-type chromosome exchanges than acute gamma rays.
- The linear dose-response term for chromosome exchanges was consistent across proton energies.
- Shielding showed minor differences, with lower RBE values for shielded compared to unshielded high-energy proton beams.
Conclusions:
- Proton radiation, particularly at higher energies, induces significant complex chromosome exchanges.
- Findings have implications for optimizing radiation protection in space and refining proton therapy techniques.
- The balance between linear energy transfer (LET) and secondary particle production influences biological response.
Related Concept Videos
Gene Conversion
10.9K
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
10.9K
Homologous Recombination
65.5K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
65.5K
Fixing Double-strand Breaks
16.2K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
16.2K
Crossing Over
7.2K
Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I,...
7.2K
Crossing Over
174.2K
Unlike mitosis, meiosis aims for genetic diversity in its creation of haploid gametes. Dividing germ cells first begin this process in prophase I, where each chromosome—replicated in S phase—is now composed of two sister chromatids (identical copies) joined centrally.
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process...
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process...
174.2K
Conservative Site-specific Recombination and Phase Variation
7.3K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
7.3K


