Estimation of the Genetic Risks of Exposure to Ionizing Radiation in Humans: Current Status and Emerging Perspectives

Abstract

The 2001 report of the United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) on ;Hereditary effects of radiation' incorporates two important concepts that have emerged from advances in radiation genetics and molecular biology: (a) most radiation-induced mutations are DNA deletions, often encompassing multiple genes; however, because of structural and functional constraints, only a proportion of induced deletions may be compatible with viability and hence recoverable in the progeny and (b) viability-compatible DNA deletions induced in human germ cells are more likely to cause multi-system developmental abnormalities rather than single-gene diseases. The work reported in this paper pursues these concepts further: it examines how mechanistic insights gained from studies of repair of radiation-induced DNA double-strand breaks (DSBs) in mammalian somatic cells and from those on the origin of deletions in human genomic disorders can be extended to germ cells the aim being the development of a framework to predict regions of the human genome that may be susceptible to radiation-induced deletions. A critical analysis of the available information permits the hypothesis that in stem cell spermatogonia, most induced deletions may arise via the non-homologous end joining (NHEJ) mechanism of DSB repair whereas in irradiated oocytes, the main mechanism is likely to be non-allelic homologous recombination (NAHR) between misaligned region-specific segmental duplications that are present in the genome (NAHR is an error-prone form of homologous recombination repair). Should this hypothesis turn out to be valid, then it is possible to build on the structural and functional aspects of genomic knowledge to devise strategies to predict where in the genome deletions may be induced by radiation, their extent and their potential phenotypes.

Direct and delayed X‐ray‐induced DNA damage in male mouse germ cells

“…Genetic risk assessment of ionizing radiation is based on the direct effects of radiation [Sankaranarayanan, 2006]. Mechanistic understanding of non-targeted effects on the germ line is necessary to determine whether it is relevant for genetic risk assessment of radiation exposure.…”

Radioprotective Effects of Quercetin and Ethanolic Extract of Propolis in Gamma-Irradiated Mice

“…Ionising radiation mostly affects DNA, either directly or by generating toxic free radicals, and induces single strand breaks, double strand breaks, oxidative damage to sugar and base residues, chromosomal aberrations, and various mutations (1). Nevertheless, it is widely applied in the treatment of many malignant diseases, but it necessarily involves exposure of non-target cells in treated patients.…”

Modelling of the populating development of the genome in the radiation condition of the environment

“…[5]. Violation ratio (1) due to any external influences: mutation, migration, and so on-leads only to a change in the next generation of gene frequency ratio (2) and recovery ratio (1).…”

“…Take into account that the X-chromosome male inherits from his mother: ( 1) ( 2) m n f n q q    . As in the case of autosomal inheritance, we consider the effects of ionizing radiation on the recessive homozygote aa.…”

“…Intensive production, extracting and use of radioactive elements, the lack of protection system and so on, as well as accidents at nuclear power plants -all these reasons lead to the fact that elevated background radiation is a source of mutations affecting the gene pool of the human population, which may cause irreversible consequences not only for living people, but also for future generations [1][2][3][4]. It is therefore interesting to consider the existence and development of the population in exposure to mutagenic ionizing radiation.…”