JOURNAL DESCRIPTION

The Medical Radiology and Radiation Safety journal ISSN 1024-6177 was founded in January 1956 (before December 30, 1993 it was entitled Medical Radiology, ISSN 0025-8334). In 2018, the journal received Online ISSN: 2618-9615 and was registered as an electronic online publication in Roskomnadzor on March 29, 2018. It publishes original research articles which cover questions of radiobiology, radiation medicine, radiation safety, radiation therapy, nuclear medicine and scientific reviews. In general the journal has more than 30 headings and it is of interest for specialists working in thefields of medicine¸ radiation biology, epidemiology, medical physics and technology. Since July 01, 2008 the journal has been published by State Research Center - Burnasyan Federal Medical Biophysical Center of Federal Medical Biological Agency. The founder from 1956 to the present time is the Ministry of Health of the Russian Federation, and from 2008 to the present time is the Federal Medical Biological Agency.

Members of the editorial board are scientists specializing in the field of radiation biology and medicine, radiation protection, radiation epidemiology, radiation oncology, radiation diagnostics and therapy, nuclear medicine and medical physics. The editorial board consists of academicians (members of the Russian Academy of Science (RAS)), the full member of Academy of Medical Sciences of the Republic of Armenia, corresponding members of the RAS, Doctors of Medicine, professor, candidates and doctors of biological, physical mathematics and engineering sciences. The editorial board is constantly replenished by experts who work in the CIS and foreign countries.

Six issues of the journal are published per year, the volume is 13.5 conventional printed sheets, 88 printer’s sheets, 1.000 copies. The journal has an identical full-text electronic version, which, simultaneously with the printed version and color drawings, is posted on the sites of the Scientific Electronic Library (SEL) and the journal's website. The journal is distributed through the Rospechat Agency under the contract № 7407 of June 16, 2006, through individual buyers and commercial structures. The publication of articles is free.

The journal is included in the List of Russian Reviewed Scientific Journals of the Higher Attestation Commission. Since 2008 the journal has been available on the Internet and indexed in the RISC database which is placed on Web of Science. Since February 2nd, 2018, the journal "Medical Radiology and Radiation Safety" has been indexed in the SCOPUS abstract and citation database.

Brief electronic versions of the Journal have been publicly available since 2005 on the website of the Medical Radiology and Radiation Safety Journal: http://www.medradiol.ru. Since 2011, all issues of the journal as a whole are publicly available, and since 2016 - full-text versions of scientific articles. Since 2005, subscribers can purchase full versions of other articles of any issue only through the National Electronic Library. The editor of the Medical Radiology and Radiation Safety Journal in accordance with the National Electronic Library agreement has been providing the Library with all its production since 2005 until now.

The main working language of the journal is Russian, an additional language is English, which is used to write titles of articles, information about authors, annotations, key words, a list of literature.

Since 2017 the journal Medical Radiology and Radiation Safety has switched to digital identification of publications, assigning to each article the identifier of the digital object (DOI), which greatly accelerated the search for the location of the article on the Internet. In future it is planned to publish the English-language version of the journal Medical Radiology and Radiation Safety for its development. In order to obtain information about the publication activity of the journal in March 2015, a counter of readers' references to the materials posted on the site from 2005 to the present which is placed on the journal's website. During 2015 - 2016 years on average there were no more than 100-170 handlings per day. Publication of a number of articles, as well as electronic versions of profile monographs and collections in the public domain, dramatically increased the number of handlings to the journal's website to 500 - 800 per day, and the total number of visits to the site at the end of 2017 was more than 230.000.

The two-year impact factor of RISC, according to data for 2017, was 0.439, taking into account citation from all sources - 0.570, and the five-year impact factor of RISC - 0.352.

Medical Radiology and Radiation Safety. 2022. Vol. 67. № 4

Transmission of Radiation-Induced Genome Instability
from Irradiated Parents to their Offspring

D.S. Oslina, V.L. Rybkina, T.V. Azizova

Southern Urals Biophysics Institute, Ozyorsk, Chelyabinsk region, Russia

Contact person: Oslina Darja Sergeevna, e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it. , This email address is being protected from spambots. You need JavaScript enabled to view it.

Abstract

Numerous studies allow to suppose a transmission of radiation-induced genome instability from irradiated parents to their offspring on cell, chromosome and molecular genetic level. This review focuses on transmission of radiation-induced genome instability from irradiated parents to their offspring. Data of genome instability in animal experiments and in offspring of occupationally exposed human or human exposed in a radiation accident, and in offspring of parents exposed to radiotherapy are reviewed. The possible mechanisms of lineage transmission of genome instability are discussed. High dose irradiation can lead to DNA damage, changes in methylation patterns and miRNAs expression in parents and their offspring and result in mutations, chromosome aberration and destabilization of genome. Non-coding RNAs (miRNA, piRNA, nsRNA) are supposed to contribute to transgenerational effects, since they can target genes, change chromatin structure and disregulate gene expression.

Keywords: ionizing radiation, transgenerational effects, genetic effects, epigenetic effects

For citation: Oslina DS, Rybkina VL, Azizova TV. Transmission of Radiation-Induced Genome Instability from Irradiated Parents to their Offspring. Medical Radiology and Radiation Safety. 2022;67(4):10-18. DOI: 10.33266/1024-6177-2022-67-4-10-18

References

1. Morgan WF. Is there a common mechanism underlying genomic instability, bystander effects and other nontargeted effects of exposure to ionizing radiation? Oncogene. 2003; 22: 7094–7099.

2. Morgan WF, Sowa MB. Non-targeted bystander effects induced by ionizing radiation. Mutation Research. 2007; 616: 159–164.

3. Kovalchuk I, Kovalchuk O. Genome Stability: From Virus to Human Application. Academic Press; 2016. 712 pp.

4. Dugan LC, Bedford JS. Are Chromosomal Instabilities Induced by Exposure of Cultured Normal Human Cells to Low- or High-LET Radiation? Radiat Res. 2003; 159(3): 301–311.

5. Patkin EL, Pavlinova LI, Sofronov GA. Influence of ecotoxicants on mammalian embryogenesis and gametogenesis: epigenetic mechanisms. Interdisciplinary scientific and applied journal "Biosphere". 2013; 5(4): 450–472.

6. Baverstock K. Why do we need a new paradigm in radiobiology? Mutation Research. 2010; 687: 3–6.

7. Little MP, Goodhead DT, Bridges BA, Bouffler SD. Evidence relevant to untargeted and transgenerational effects in the offspring of irradiated parents. Mutation Research. 2013; 753(1): 50–67.

8. Committee on Medical Aspects of Radiation in the Environment (COMARE). Seventh Report. Chilton, National Radiological Protection Board; 2002. Parents occupationally exposed to radiation prior to the conception of their children. A review of the evidence concerning the incidence of cancer in their children.

9. Committee on Medical Aspects of Radiation in the Environment (COMARE). Eighth Report. Chilton, National Radiological Protection Board; 2004. Review of pregnancy outcomes following preconceptional exposure to radiation.

10. Slovinská L, Elbertová A, Mišúrová E. Transmission of genome damage from irradiated male rats to their progeny. Mutation Research. 2004: 559; 29–37.

11. Mughal SK, Myazin AE, Zhavoronkov LP, Mughal SK, Myazin AE, Zhavoronkov LP, Rubanovich AV, Dubrova YE. The dose and dose-rate effects of paternal irradiation on transgenerational instability in mice: a radiotherapy connection. PLoS One. 2012; 7(7): 1−5.

12. Glen CD, Dubrova YE. Exposure to anticancer drugs can result in transgenerational genomic instability in mice. Proc Natl Acad Sci USA. 2012; 109: 2984–2988.

13. Lomaeva MG, Vasil’eva GV, Fomenko LA, Antipova VN, Gaziev AI, Bezlepkin VG. Increased Genomic Instability in Somatic Cells of the Progeny of Female Mice Exposed to Acute X−Radiation in the Preconceptional Period. Rus J Genetics. 2011; 47(10): 1221.

14. Lomaeva МG, Fomenko LA, Vasil’eva GV, Bezlepkin VG. Tissue-specific Changes in the Polymorphism of Simple Repeats in DNA of the Offspring of Different Sex Born from Irradiated Male or Female Mice. Radiation biology. Radioecology. 2016; 56(2): 149–155.

15. Nefedov IY, Nefedova IY, Palyga GF. Actual aspects of the problem of the genetic consequences of mammalian exposure. Radiation biology. Radioecology. 2000; 40(4); 358–372.

16. Abouzeid AHE, Barber RC, Dubrova YE. The effects of maternal irradiation during adulthood on mutation induction and transgenerational instability in mice. Mutation Research. 2012; 732: 21–25.

17. Somers CM. Expanded simple tandem repeat (ESTR) mutation induction in the male germline: lessons learned from lab mice. Mutation Research. 2006; 598: 35–49.

18. Barber RC, Hickenbotham P, Hatch T, Kelly D, Topchiy N, Almeida GM, Jones GD, Johnson GE, Parry JM, Rothkamm K, Dubrova YE. Radiation-induced transgenerational alterations in genome stability and DNA damage. Oncogene. 2006; 25: 7336–7342.

19. Min H, Sung M, Son M, Kawasaki I, Shim YH. Transgenerational effects of proton beam irradiation on Caenorhabditis elegans germline apoptosis. Biochemical and Biophysical Research Communications. 2017; 490(3): 608–615.

20. Parisot F, Bourdineaud JP, Plaire D, Adam-Guillermin C, Alonzo F. DNA alterations and effects on growth and reproduction in Daphnia magna during chronic exposure to gamma radiation over three successive generations. Aquatic Toxicology. 2015; 163: 27–36.

21. Sarapultseva EI, Dubrova YE. The long-term effects of acute exposure to ionising radiation on survival and fertility in Daphnia magna. Environmental Research. 2016; 150: 138–143.

22. Smith RW, Seymour CB, Moccia RD, Mothersill CE. Irradiation of rainbow trout at early life stages results in trans-generational effects including the induction of a bystander effect in non-irradiated fish. Environmental Research. 2016; 145: 26–38. 

23. Shimada Atsuko, Shima Akihiro. Transgenerational genomic instability as revealed by a somatic mutation assay using the medaka fish. Mutation Research. 2004; 552: 119–124. 

24. Tsyusko O, Glenn T, Yi Y, Joice G, Jones K, Aizawa K, Coughlin D, Zimbrick J, Hinton T. Differential genetic responses to ionizing irradiation in individual families of Japanese medaka. Mutation Research. 2011; 718: 18–23.

25. Hurem S, Gomes T, Brede DA, Lindbo Hansen E, Mutoloki S, Fernandez C, Mothersill C, Salbu B, Kassaye YA, Olsen AK, Oughton D, Aleström P, Lyche JL. Parental gamma irradiation induces reprotoxic effects accompanied by genomic instability in zebrafish (Danio rerio) embryos. Environmental Research. 2017; 159: 564–578.

26. Hurem S, Martín LM, Lindeman L, Brede DA, Salbu B, Lyche JL, Aleström P, Kamstra JH. Parental exposure to gamma radiation causes progressively altered transcriptomes linked to adverse effects in zebrafish offspring. Environmental Pollution. 2018; 234: 855–863.

27. Gardner MJ, Snee MP, Hall AJ, Powell CA, Downes S, Terrell JD. Results of case-control study of leukaemia and lymphoma among young people near Sellafield nuclear plant in West Cumbria. BMJ. 1990; 300: 423–429.

28. Dubrova YE, Bersimbaev RI, Djansugurova LB, Tankimanova MK, Mamyrbaeva ZZh, Mustonen R, Lindholm C, Hultén M, Salomaa S. Nuclear weapons tests and human germline mutation rate. Science. 2002; 295: 1037.

29. Livshits LA, Malyarchuk SG, Kravchenko SA, Lukyanova EM, Antipkin YG, Arabskaya LP, Matsuka GH, Petit E, Giraudeau F, Gourmelon P, Vergnaud G, Le Guen B. Children of Chernobyl cleanup workers do not show elevated rates of mutations in minisatellite alleles. Radiation Research. 2001; 155: 74–80.

30. Furitsu K, Ryo H, Yeliseeva KG, Thuy le TT, Kawabata H, Krupnova EV, Trusova VD, Rzheutsky VA, Nakajima H, Kartel N, Nomura T. Microsatellite mutations show no increases in the children of the Chernobyl liquidators. Mutation Research. 2005; 581: 69–82.

31. Kiuru A, Auvinen A, Luokkamaki M, Makkonen K, Veidebaum T, Tekkel M, Rahu M, Hakulinen T, Servomaa K, Rytömaa T, Mustonen R. Hereditary minisatellite mutations among the offspring of Estonian Chernobyl cleanup workers. Radiation Research. 2003; 159: 651–655.

32. Kodaira M, Izumi S. Takahashi N, Nakamura N. No evidence of radiation effect on mutation rates at hypervariable minisatellite loci in the germ cells of atomic bomb survivors. Radiation Research. 2004; 162: 350–356.

33. Bezlepkin VG, Kirillova EN, Zakharova ML, Pavlova OS, Lomaeva MG, Fomenko LA, Antipova VN, Gaziev AI. Delayed and Transgenerational Molecular and Genetic Effects of Prolonged Influence of Ionizing Radiation in Nuclear Plant Workers. Radiation biology. Radioecology. 2011; 51(1); 20–32.

34. Rees GS, Trikik MZ, Winther JF, Tawn EJ, Stovall M, Olsen JH, Rechnitzer C, Schrøder H, Guldberg P, Boice JD Jr. A pilot study examining germline minisatellite mutations in the offspring of Danish childhood and adolescent cancer survivors treated with radiotherapy. Int J Radiat Biol. 2006; 82(3): 153–160.

35. Vignard J, Mirey G, Salles B. Ionizing-radiation induced DNA double-strand breaks: A direct and indirect lighting up. Radiotherapy and Oncology. 2013; 108: 362–369.

36. Tawn EJ, Whitehouse CA, Winther JF, Curwen GB, Rees GS, Stovall M, Olsen JH, Guldberg P, Rechnitzer C, Schrøder H, Boice JD Jr. Chromosome analysis in childhood cancer survivors and their offspring – no evidence for radiotherapy-induced persistent genomic instability. Mutation Research. 2005; 583: 198–206.

37. Signorello LB, Mulvihill JJ, Green DM, Munro HM, Stovall M, Weathers RE, Mertens AC, Whitton JA, Robison LL, Boice JD Jr. Stillbirth and neonatal death in relation to radiation exposure before conception: a retrospective cohort study. Lancet. 2010; 376: 624–630.

38. Kuzmina NS, Lapteva NSh, Rubanovich AV. Hypermethylation of gene promoters in peripheral blood leukocytes in humans longterm after radiation exposure. Environmental Research. 2016; 146: 10–17.

39. Suzuki R, Ojima M, Kodama S, Watanabe M. Delayed activation of DNA damage checkpoint and radiation-induced genomic instability. Mutat Res. 2006; 597 (1–2): 73–77.

40. Venkatesan S, Natarajan AT, Hande M. Chromosomal instability—mechanisms and consequences. Mutation Research. 2015; 793: 176–184.

41. Sabatier L, Ricoul M, Pottier G, Murnane JP. The loss of single telomere can result in instability of multiple chromosomes in a human tumor cell line. Mol Cancer Res. 2005; 3: 139–150.

42. Blake GET, Watson ED. Unravelling the complex mechanisms of transgenerational epigenetic inheritance. Current Opinion in Chemical Biology. 2016; 33: 101–107.

43. Molla-Herman A, Matias NR, Huynh JR. Chromatin modifications regulate germ cell development and transgenerational information relay. Current Opinion in Insect Science. 2014; 1: 10–18.

44. Pogribny I, Koturbash I, Tryndyak V, Hudson D, Stevenson SML, Sedelnikova O, Bonner W, Kovalchuk O. Fractionated low-dose radiation exposure leads to accumulation of DNA damage and profound alterations in DNA and histone methylation in the murine thymus. Mol Cancer Res. 2005; 3(10): 553–561. 

45. Kovalchuk O, Burke P, Besplug J, Slovack M, Filkowski J, Pogribny I. Methylation changes in muscle and liver tissues of male and female mice exposed to acute and chronic low-dose X-ray-irradiation. Mutation Research. 2004; 548: 75–84.

46. Koturbash I, Boyko A, Rodriguez-Juarez R, McDonald RJ, Tryndyak VP, Kovalchuk I, Pogribny IP, Kovalchuk O. Role of epigenetic effectors in maintenance of the long-term persistent bystander effect in spleen in vivo. Carcinogenesis. 2007; 28(8): 1831–1838.

47. Transgenerational Epigenetics / ed. Tollefsbol T. Academic Press, 2014. 412 pp. http://dx.doi.org/10.1016/B978-0-12-405944-3.00011-8.

48. Niwa O. Indirect mechanisms of radiation induced genomic instability at repeat loci // International Congress Series. 2007; 1299: 135–145. 

49. Scully R, Xie A. Double strand break repair functions of histone H2AX. Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis. 2013; 750 (1–2):5–14.

50. Vasilyev S, Velichevskaya AI, Vishnevskaya TV, Belenko AA, Gribova O, Plaksin MB, Startseva ZhA, Lebedev I. Background Level of γH2AX Foci in Human Cells as a Factor of Individual Radiosensitivity. Radiation biology. Radioecology. 2015; 55(4): 402–410.

51. Merrifield M, Kovalchuk O. Sins of Fathers Through a Scientific Lens: Transgenerational Effects Genome Stability. http://dx.doi.org/10.1016/B978-0-12-803309-8.00034-3

52. Ahmad P, Sana J, Slavik M, Slampa P, Smilek P, Slaby O. MicroRNAs Involvement in Radioresistance of Head and Neck Cancer. Disease Markers. 2017. Article ID 8245345. http://dx.doi.org/10.1155/2017/8245345

53. Ilnytskyy Y, Zemp FJ, Koturbash I, Kovalchuk O. Altered microRNA expression patterns in irradiated hematopoietic tissues suggest a sex-specific protective mechanism. Biochemical and Biophysical Research Communications. 2008; 377: 41–45.

54. Barber RC, Dubrova YE, Gant TW. Radiation-induced transgenerational alterations in MicroRNA expression. Toxicology. 2011; 290: 1–46.

55. Filkowski JN, Ilnytskyy Y, Tamminga J, Koturbash I, Golubov A, Bagnyukova T, Pogribny IP, Kovalchuk O. Hypomethylation and genome instability in the germline of exposed parents and their progeny is associated with altered miRNA expression. Carcinogenesis. 2010; 6: 1110–1115.

56. Aravin AA, Sachidanandam R, Bourc’his D, Schaefer C, Pezic D, Fejes Toth K, Bestor T, Hannon GJ. A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice. Mol Cell. 2008; 31(6): 785–799.

57. Thomson T, Lin H. The biogenesis and function of PIWI proteins and piRNAs: progress and prospect. Annu Rev Cell Dev Biol. 2009; 25: 355–376.

58. Rechavi O, Houri-Ze’evi L, Anava S, Goh WSS, Kerk SY, Hannon GJ, Hobert O. Starvation-Induced Transgenerational Inheritance of Small RNAs in C. elegans. Cell. 2014; 158: 277–287. 

59. Nelson VR Nadeau JH. Transgenerational genetic effects. Epigenomics. 2010; 2(6):797–806.

 PDF (RUS) Full-text article (in Russian)

Conflict of interest. The authors declare no conflict of interest.

Financing. The study had no sponsorship.

Contribution. Article was prepared with equal participation of the authors.

Article received: 15.03.2022.  Accepted for publication: 11.05.2022

 

 

 

Contact Information

 

46, Zhivopisnaya st., 123098, Moscow, Russia Phone: +7 (499) 190-95-51. E-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Journal location

Attendance

2766802
Today
Yesterday
This week
Last week
This month
Last month
For all time
2696
4471
25186
18409
74545
75709
2766802

Forecast today
2952


Your IP:216.73.216.90