A U-shaped doseresponse relationship between X Radiation and sex-linked recessive lethal mutation in male germ cells of drosophila

Radiation Research

Volumn 174, Issue 1, 2010, Pages 46-51

  Koana, Takao ^a   Tsujimura, Hidenobu ^b  

^a CENTRAL RESEARCH INSTITUTE OF ELECTRIC POWER INDUSTRY   (Japan)

^b TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; APOPTOSIS; ARTICLE; CONTROLLED STUDY; DOSE RESPONSE; DROSOPHILA; EXCISION REPAIR; FEMALE; GENE MUTATION; GERM CELL; IONIZING RADIATION; IRRADIATION; LETHAL MUTANT; LOW ENERGY RADIATION; MALE; MUTATION RATE; NONHUMAN; PRIORITY JOURNAL; RADIATION DOSE; RECESSIVE INHERITANCE; X RAY; ANIMAL; DROSOPHILA MELANOGASTER; GENETICS; LETHAL GENE; MUTATION; NICK END LABELING; RADIATION EXPOSURE; RECESSIVE GENE; SPERMATOZOON;

DROSOPHILA MELANOGASTER;

ANIMALS; DOSE-RESPONSE RELATIONSHIP, DRUG; DROSOPHILA MELANOGASTER; FEMALE; GENES, LETHAL; GENES, RECESSIVE; IN SITU NICK-END LABELING; MALE; MUTATION; SPERMATOZOA;

EID: 77954491156     PISSN: 00337587     EISSN: None     Source Type: Journal    
DOI: 10.1667/RR2085.1     Document Type: Article

References (33)

1. C. P. Oliver, The effect of varying the duration of X-ray treatment upon the frequency of mutation. Science 71, 44-46 (1930).
2. K. Sankaranarayanan and F. H. Sobels, Radiation genetics. In The Genetics and Biology of Drosophila (M. Ashburner and E. Novitski, Eds.), Vol.1c, pp. 1089-1250. Academic Press, London, 1976.
3. W. L. Russell and E. M. Kelley, Specific-locus mutation frequencies in mouse stem-cell spermatogonia at very low radiation dose rate. Proc. Natl. Acad. Sci. USA 79, 539-541 (1982).
4. W. L. Russell and E. M. Kelley, Mutation frequency in male mice and the estimation of genetic hazard of radiation in men. Proc. Natl. Acad. Sci. USA 79, 542-544 (1982).
5. National Research Council, Committee on Health Risks from Exposure to Low Levels of Ionizing Radiation, Health Risks from Exposure to Low Levels of Ionizing Radiation: BEIR VII Phase 2, pp. 43-64. National Academies Press, Washington, DC, 2006.
6. UNSCEAR, Effects of Ionizing Radiation: UNSCEAR 2006 Report, Annex C. United Nations, New York, 2006.
7. K. Prise, O. V. Belyakov, H. C. Newman, S. Patel, G. Schettino, M. Folkard and B. D. Michael, Non-targeted effects of radiation: bystander response in cell and tissue models. Radiat. Prot. Dosimetry 99, 223-226 (2002).
8. 2-phase cells. Radiat. Res. 161, 247-255 (2004).
9. E. J. Hall and T. K. Hei, Genomic instability and bystander effects induced by high-LET radiation. Oncogene 22, 7034-7042 (2003).
10. J. Magae, Y. Hoshi, C. Furukawa, Y. Kawakami and H. Ogata, Quantitative analysis of biological responses to ionizing radiation, including dose, irradiation time, and dose rate. Radiat. Res. 160, 543-548 (2003).
11. 0 lymphocytes exposed in vitro to gamma radiation. Radiat. Res. 165, 43-50 (2006).
12. K. Otsuka, T. Koana, M. Tomita, H. Ogata and H. Tauchi, Rapid myeloid recovery as a possible mechanism of whole-body radioadaptive response. Radiat. Res. 170, 307-315 (2008).
13. Y. Fan and A. Bergmann, Apoptosis-induced compensatory proliferation. The cell is dead. Long live the cell! Trends Cell Biol. 18, 467-473 (2008).
14. J. Blatt, J. J. Mulvihill, J. L. Ziegler, R. C. Young and D. G. Poplack, Pregnancy outcome following cancer chemotherapy. Am. J. Med. 69, 828-832 (1980).
15. R. Sankila, J. H. Olsen, H. Anderson, S. Garwicz, E. Glattre, H. Hertz, F. Langmark, M. Lanning, T. Moller and H. Tulinius, Risk of cancer among offspring of childhood-cancer survivors. Association of the Nordic Cancer Registries and the Nordic Society of Paediatric Haematology and Oncology. N. Engl. J. Med. 338, 1339-1344 (1998).
16. M. M. Hawkins, D. L. Winter, H. S. Burton and M. H. Potok, Heri-tability of Wilms' tumor. J. Natl. Cancer Inst. 87, 1323-1324 (1995).
17. R. Nagarajan and L. L. Robinson, Pregnancy outcomes in survivors of childhood cancer. J. Natl. Cancer Inst. Monogr. 34, 72-76 (2005).
18. J. Byrne, J. J. Mulvihill, R. R. Connelly, D. A. Austin, G. E. Holmes, F. F. Holmes, H. B. Laourette, J. W. Meigs, L. C. Strong and M. H. Myers, Reproductive problems and birth defects in survivors of Wilms' tumor and their relatives. Med. Pediatr. Oncol. 16, 233-240 (1988).
19. T. Koana, M. O. Okada, K. Ogura, H. Tsujimura and K. Sakai, Reduction of background mutations by low-dose X irradiation of Drosophila spermatocytes at a low dose rate. Radiat. Res. 167, 217-221 (2007).
20. T. Koana, Y. Takashima, M. O. Okada, M. Ikehata, J. Miyakoshi and K. Sakai, A threshold exists in the dose-response relationship for somatic mutation frequency induced by X irradiation of Drosophila. Radiat. Res. 161, 391-396 (2004).
21. A. H. Yamamoto, R. K. Brodberg, S. S. Banga, J. B. Boyd and J. M. Mason, Recovery and characterization of hybrid dysgenesis-induced mei-9 and mei-41 alleles of Drosophila melanogaster. Mutat. Res. 229, 17-28 (1990).
22. D. L. Lindsley and G. G. Zimm, The Genome of Drosophila melanogaster. Academic Press, San Diego, 1992.
23. FlyBase, a database of the Drosophila genome. Available online at http://flybase.org/.
24. D. L. Hartl and E. W. Jones, Essential Genetics: A Genomics Perspective. Jones and Bartlett, Sudbury, MA, 2002.
25. K. Kimura, Programmed cell death in Drosophila melanogaster. Exp. Med. 11, 2248-2254 (1995). [in Japanese]
26. K. Ogura, J. Magae, Y. Kawakami and T. Koana, Reduction in mutation frequency by very low-dose gamma irradiation of Drosophila melanogaster. Radiat. Res. 171, 1-8 (2009).
27. K. L. Hari, A. Santerre, J. J. Sekelesky, K. S. McKim, J. B. Boid and R. S. Hawley, The mei-41 gene of D. melanogaster is a structural and functional homolog of the human Ataxia telangiectasia gene. Cell 82, 815-821 (1995).
28. M. Yonezawa, J. M sonoh and Y. Hosokawa, Two types of X-ray-induced radioresistance in mice: Presence of 4 dose range with distinct biological effects. Mutat. Res. 358, 237-243 (1996).
29. K. Otsuka, T. Koana, H. Tauchi and K. Sakai, Activation of antioxidative enzymes induced by low-dose-rate whole-body c irradiation: Adaptive response in terms of initial DNA damage, Radiat. Res. 166, 474-478 (2006).
30. E. L. Azzam, S. M. de Toledo, G. P. Raaphorst and R. E. Mitchel, Low-dose ionizing radiation decreases the frequency of neoplastic transformation to a level below the spontaneous rate in C3H 10TK cells. Radiat. Res. 146, 369-373 (1996).
31. A. M. Hooker, B. Madhava, T. K. Day, J. M. Lane, S. J. Swinburne, A. A. Morley and P. J. Sykes, The linear no-threshold model does not hold for low-dose ionizing radiation. Radiat. Res. 163, 447-452 (2004).
32. K. Kant, R. P. Chauhan, G. S. Sharma and S. K. Chakarvarti, Hormesis in humans exposed to low-level ionizing radiation. Int. J. Low Radiat. 1, 76-87 (2003).
33. S. M. de Toledo and E. I. Azzam, Adaptive and bystander responses in human and rodent cell cultures exposed to low level ionizing radiation: the impact of linear energy transfer. Dose-Response 4, 291-301 (2006).