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. 1994 Apr;136(4):1401–1420. doi: 10.1093/genetics/136.4.1401

Efficient Recovery of Enu-Induced Mutations from the Zebrafish Germline

L Solnica-Krezel 1, A F Schier 1, W Driever 1
PMCID: PMC1205920  PMID: 8013916

Abstract

We studied the efficiency with which two chemical mutagens, ethyl methanesulfonate (EMS) and N-ethyl-N-nitrosourea (ENU) can induce mutations at different stages of spermatogenesis in zebrafish (Brachydanio rerio). Both EMS and ENU induced mutations at high rates in post-meiotic germ cells, as indicated by the incidence of F(1) progeny mosaic for the albino mutation. For pre-meiotic germ cells, however, only ENU was found to be an effective mutagen, as indicated by the frequencies of non-mosaic mutant progeny at four different pigmentation loci. Several mutagenic regimens that varied in either the number of treatments or the concentration of ENU were studied to achieve an optimal ratio between the mutagenicity and toxicity. For the two most mutagenic regimens: 4 X 1 hr in 3 mM ENU and 6 X 1 hr in 3 mM ENU, the minimum estimate of frequencies of independent mutations per locus per gamete was 0.9-1.3 X 10(-3). We demonstrate that embryonic lethal mutations induced with ENU were transmitted to offspring and that they could be recovered in an F(2) screen. An average frequency of specific-locus mutations of 1.1 X 10(-3) corresponded to approximately 1.7 embryonic lethal mutations per single mutagenized genome. The high rates of mutations achievable with ENU allow for rapid identification of large numbers of genes involved in a variety of aspects of zebrafish development.

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Selected References

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  1. CARTER T. C. Recessive lethal mutation induced in the mouse by chronic gamma-irradiation. Proc R Soc Lond B Biol Sci. 1957 Dec 3;147(928):402–411. doi: 10.1098/rspb.1957.0059. [DOI] [PubMed] [Google Scholar]
  2. Chakrabarti S., Streisinger G., Singer F., Walker C. Frequency of gamma-Ray Induced Specific Locus and Recessive Lethal Mutations in Mature Germ Cells of the Zebrafish, BRACHYDANIO RERIO. Genetics. 1983 Jan;103(1):109–123. doi: 10.1093/genetics/103.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Culp P., Nüsslein-Volhard C., Hopkins N. High-frequency germ-line transmission of plasmid DNA sequences injected into fertilized zebrafish eggs. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7953–7957. doi: 10.1073/pnas.88.18.7953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ehling U. H., Cumming R. B., Malling H. V. Induction of dominant lethal mutations by alkylating agents in male mice. Mutat Res. 1968 May-Jun;5(3):417–428. doi: 10.1016/0027-5107(68)90011-0. [DOI] [PubMed] [Google Scholar]
  5. FAHMY O. G., FAHMY M. J. Mutagenic response to the alkyl-methanesulphonates during spermatogenesis in Drosophila melanogaster. Nature. 1957 Jul 6;180(4575):31–34. doi: 10.1038/180031a0. [DOI] [PubMed] [Google Scholar]
  6. Favor J., Neuhäuser-Klaus A., Ehling U. H. The frequency of dominant cataract and recessive specific-locus mutations and mutation mosaics in F1 mice derived from post-spermatogonial treatment with ethylnitrosourea. Mutat Res. 1990 Apr;229(2):105–114. doi: 10.1016/0027-5107(90)90084-h. [DOI] [PubMed] [Google Scholar]
  7. Favor J., Sund M., Neuhäuser-Klaus A., Ehling U. H. A dose-response analysis of ethylnitrosourea-induced recessive specific-locus mutations in treated spermatogonia of the mouse. Mutat Res. 1990 Jul;231(1):47–54. doi: 10.1016/0027-5107(90)90175-4. [DOI] [PubMed] [Google Scholar]
  8. Felsenfeld A. L., Walker C., Westerfield M., Kimmel C., Streisinger G. Mutations affecting skeletal muscle myofibril structure in the zebrafish. Development. 1990 Mar;108(3):443–459. doi: 10.1242/dev.108.3.443. [DOI] [PubMed] [Google Scholar]
  9. Grunwald D. J., Streisinger G. Induction of mutations in the zebrafish with ultraviolet light. Genet Res. 1992 Apr;59(2):93–101. doi: 10.1017/s0016672300030305. [DOI] [PubMed] [Google Scholar]
  10. Grunwald D. J., Streisinger G. Induction of recessive lethal and specific locus mutations in the zebrafish with ethyl nitrosourea. Genet Res. 1992 Apr;59(2):103–116. doi: 10.1017/s0016672300030317. [DOI] [PubMed] [Google Scholar]
  11. Harbach P. R., Filipunas A. L., Wang Y., Aaron C. S. DNA sequence analysis of spontaneous and N-ethyl-N-nitrosourea-induced hprt mutations arising in vivo in cynomolgus monkey T-lymphocytes. Environ Mol Mutagen. 1992;20(2):96–105. doi: 10.1002/em.2850200205. [DOI] [PubMed] [Google Scholar]
  12. Hatta K., Kimmel C. B., Ho R. K., Walker C. The cyclops mutation blocks specification of the floor plate of the zebrafish central nervous system. Nature. 1991 Mar 28;350(6316):339–341. doi: 10.1038/350339a0. [DOI] [PubMed] [Google Scholar]
  13. Hitotsumachi S., Carpenter D. A., Russell W. L. Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6619–6621. doi: 10.1073/pnas.82.19.6619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Johnson F. M., Lewis S. E. Electrophoretically detected germinal mutations induced in the mouse by ethylnitrosourea. Proc Natl Acad Sci U S A. 1981 May;78(5):3138–3141. doi: 10.1073/pnas.78.5.3138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kimmel C. B. Genetics and early development of zebrafish. Trends Genet. 1989 Aug;5(8):283–288. doi: 10.1016/0168-9525(89)90103-0. [DOI] [PubMed] [Google Scholar]
  16. Kimmel C. B., Kane D. A., Walker C., Warga R. M., Rothman M. B. A mutation that changes cell movement and cell fate in the zebrafish embryo. Nature. 1989 Jan 26;337(6205):358–362. doi: 10.1038/337358a0. [DOI] [PubMed] [Google Scholar]
  17. Lefevre G., Watkins W. The question of the total gene number in Drosophila melanogaster. Genetics. 1986 Aug;113(4):869–895. doi: 10.1093/genetics/113.4.869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Loveless A. Possible relevance of O-6 alkylation of deoxyguanosine to the mutagenicity and carcinogenicity of nitrosamines and nitrosamides. Nature. 1969 Jul 12;223(5202):206–207. doi: 10.1038/223206a0. [DOI] [PubMed] [Google Scholar]
  19. McDonald J. D., Bode V. C., Dove W. F., Shedlovsky A. Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase. Proc Natl Acad Sci U S A. 1990 Mar;87(5):1965–1967. doi: 10.1073/pnas.87.5.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Moser A. R., Pitot H. C., Dove W. F. A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse. Science. 1990 Jan 19;247(4940):322–324. doi: 10.1126/science.2296722. [DOI] [PubMed] [Google Scholar]
  21. Nüsslein-Volhard C., Wieschaus E. Mutations affecting segment number and polarity in Drosophila. Nature. 1980 Oct 30;287(5785):795–801. doi: 10.1038/287795a0. [DOI] [PubMed] [Google Scholar]
  22. Popp R. A., Bailiff E. G., Skow L. C., Johnson F. M., Lewis S. E. Analysis of a mouse alpha-globin gene mutation induced by ethylnitrosourea. Genetics. 1983 Sep;105(1):157–167. doi: 10.1093/genetics/105.1.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. RUSSELL W. L. X-ray-induced mutations in mice. Cold Spring Harb Symp Quant Biol. 1951;16:327–336. doi: 10.1101/sqb.1951.016.01.024. [DOI] [PubMed] [Google Scholar]
  24. Richardson K. K., Richardson F. C., Crosby R. M., Swenberg J. A., Skopek T. R. DNA base changes and alkylation following in vivo exposure of Escherichia coli to N-methyl-N-nitrosourea or N-ethyl-N-nitrosourea. Proc Natl Acad Sci U S A. 1987 Jan;84(2):344–348. doi: 10.1073/pnas.84.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Rinchik E. M. Chemical mutagenesis and fine-structure functional analysis of the mouse genome. Trends Genet. 1991 Jan;7(1):15–21. doi: 10.1016/0168-9525(91)90016-j. [DOI] [PubMed] [Google Scholar]
  26. Russell L. B., Selby P. B., von Halle E., Sheridan W., Valcovic L. The mouse specific-locus test with agents other than radiations: interpretation of data and recommendations for future work. Mutat Res. 1981 May;86(3):329–354. doi: 10.1016/0165-1110(81)90010-5. [DOI] [PubMed] [Google Scholar]
  27. Sega G. A. Unscheduled DNA synthesis in the germ cells of male mice exposed in vivo to the chemical mutagen ethyl methanesulfonate. Proc Natl Acad Sci U S A. 1974 Dec;71(12):4955–4959. doi: 10.1073/pnas.71.12.4955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Shedlovsky A., Guenet J. L., Johnson L. L., Dove W. F. Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen. Genet Res. 1986 Apr;47(2):135–142. doi: 10.1017/s0016672300022977. [DOI] [PubMed] [Google Scholar]
  29. Shedlovsky A., King T. R., Dove W. F. Saturation germ line mutagenesis of the murine t region including a lethal allele at the quaking locus. Proc Natl Acad Sci U S A. 1988 Jan;85(1):180–184. doi: 10.1073/pnas.85.1.180. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Shima A., Shimada A. Development of a possible nonmammalian test system for radiation-induced germ-cell mutagenesis using a fish, the Japanese medaka (Oryzias latipes). Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2545–2549. doi: 10.1073/pnas.88.6.2545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Streisinger G., Singer F., Walker C., Knauber D., Dower N. Segregation analyses and gene-centromere distances in zebrafish. Genetics. 1986 Feb;112(2):311–319. doi: 10.1093/genetics/112.2.311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Streisinger G., Walker C., Dower N., Knauber D., Singer F. Production of clones of homozygous diploid zebra fish (Brachydanio rerio). Nature. 1981 May 28;291(5813):293–296. doi: 10.1038/291293a0. [DOI] [PubMed] [Google Scholar]
  33. Vogel E. W., Blijleven W. G., Kortselius M. J., Zijlstra J. A. A search for some common characteristics of the effects of chemical mutagens in Drosophila. Mutat Res. 1982 Feb 22;92(1-2):69–87. doi: 10.1016/0027-5107(82)90211-1. [DOI] [PubMed] [Google Scholar]
  34. Walker C., Streisinger G. Induction of Mutations by gamma-Rays in Pregonial Germ Cells of Zebrafish Embryos. Genetics. 1983 Jan;103(1):125–136. doi: 10.1093/genetics/103.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Westerfield M., Liu D. W., Kimmel C. B., Walker C. Pathfinding and synapse formation in a zebrafish mutant lacking functional acetylcholine receptors. Neuron. 1990 Jun;4(6):867–874. doi: 10.1016/0896-6273(90)90139-7. [DOI] [PubMed] [Google Scholar]
  36. Youvan D. C., Ismail S. Light-harvesting II (B800-B850 complex) structural genes from Rhodopseudomonas capsulata. Proc Natl Acad Sci U S A. 1985 Jan;82(1):58–62. doi: 10.1073/pnas.82.1.58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. van Zeeland A. A., Mohn G. R., Neuhäuser-Klaus A., Ehling U. H. Quantitative comparison of genetic effects of ethylating agents on the basis of DNA adduct formation. Use of O6-ethylguanine as molecular dosimeter for extrapolation from cells in culture to the mouse. Environ Health Perspect. 1985 Oct;62:163–169. doi: 10.1289/ehp.8562163. [DOI] [PMC free article] [PubMed] [Google Scholar]

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