Literature DB >> 22397578

The effect of dose rate on the frequency of specific-locus mutations induced in mouse spermatogonia is restricted to larger lesions; a retrospective analysis of historical data.

Liane B Russell1, Patricia R Hunsicker.   

Abstract

A series of 19 large-scale germ-cell mutagenesis experiments conducted several decades ago led to the conclusion that low-LET radiation delivered to mouse spermatogonia at dose rates of 0.8 R/min and below induced only about one-third as many specific-locus mutations as did single, acute exposures at 24 R/min and above. A two-hit origin of the mutations was deemed unlikely in view of the then prevailing evidence for the small size of genetic lesions in spermatogonia. Instead, the dose-rate effect was hypothesized to be the result of a repair system that exists in spermatogonia, but not in more mature male reproductive cells. More recent genetic and molecular studies on the marker genes have identified the phenotypes associated with specific states of the mutant chromosomes, and it is now possible retrospectively to classify individual past mutations as "large lesions" or "other lesions". The mutation-frequency difference between high and low dose rates is restricted to the large lesion mutations, for which the dose-curve slopes differ by a factor exceeding 3.4. For other lesion mutations, there is essentially no difference between the slopes for protracted and acute irradiations; induced other lesions frequencies per unit dose remain similar for dose rates ranging over more than 7 orders of magnitude. For large lesions, these values rise sharply at dose rates >0.8 R/min, though they remain similar within the whole range of protracted doses, failing to provide evidence for a threshold dose rate. The downward bend at high doses that had been noted for X-ray-induced specific-locus mutations as a whole and ascribed to a positive correlation between spermatogonial death and mutation load is now found to be restricted to large lesion mutations. There is a marked difference between the mutation spectra (distributions among the seven loci) for large lesions and other lesions. Within each class, however, the spectra are similar for acute and protracted irradiation.

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Year:  2012        PMID: 22397578     DOI: 10.1667/rr2853.1

Source DB:  PubMed          Journal:  Radiat Res        ISSN: 0033-7587            Impact factor:   2.841


  5 in total

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Journal:  Life Sci Space Res (Amst)       Date:  2016-05-21

2.  Increased Frequency of Copy Number Variations Revealed by Array Comparative Genomic Hybridization in the Offspring of Male Mice Exposed to Low Dose-Rate Ionizing Radiation.

Authors:  Keiji Ogura; Yoshiko Ayabe; Chihiro Harada; Ignacia Braga Tanaka; Satoshi Tanaka; Jun-Ichiro Komura
Journal:  Int J Mol Sci       Date:  2021-11-18       Impact factor: 5.923

3.  Induction of somatic mutations by low concentrations of tritiated water (HTO): evidence for the possible existence of a dose-rate threshold.

Authors:  Haruki Nagashima; Yuki Hayashi; Yuki Sakamoto; Kenshi Komatsu; Hiroshi Tauchi
Journal:  J Radiat Res       Date:  2021-07-10       Impact factor: 2.724

Review 4.  The role of dose rate in radiation cancer risk: evaluating the effect of dose rate at the molecular, cellular and tissue levels using key events in critical pathways following exposure to low LET radiation.

Authors:  Antone L Brooks; David G Hoel; R Julian Preston
Journal:  Int J Radiat Biol       Date:  2016-06-07       Impact factor: 2.694

5.  Induction of somatic mutations by low-dose X-rays: the challenge in recognizing radiation-induced events.

Authors:  Haruki Nagashima; Kumiko Shiraishi; Saori Ohkawa; Yuki Sakamoto; Kenshi Komatsu; Shinya Matsuura; Akira Tachibana; Hiroshi Tauchi
Journal:  J Radiat Res       Date:  2018-04-01       Impact factor: 2.724

  5 in total

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