Skip to main content
Log in

The Oenothera plastome mutator : effect of UV irradiation and nitroso-methyl urea on mutation frequencies

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

Oenothera plants homozygous for a recessive plastome mutator allele (pm) showed spontaneous mutation frequencies for plastome genes that are 200-fold higher than spontaneous levels. Mutations occurred at high frequencies in plants grown in the field, in a glass-house, or as leaf tip cultures under fluorescent light, indicating that the plastome mutator activity is UV-independent. However, the chlorotic sectors became visible at an earlier stage of development when seedlings were irradiated, compared to seedlings that were not exposed to UV. These results imply that the rate of sorting-out was increased by the irradiation treatment, possibly due to a decrease in the effective number of multiplication-competent plastids, or a reduction in the extent of cytoplasmic mixing. Nitroso-methyl urea treatment of seeds had a dramatic effect on mutation frequency in both wild-type and plastome mutator samples. When the background mutation rates were low, the combination of the plastome mutator nucleus and the chemical mutagenesis treatment resulted in a synergistic effect, suggesting that the plastome mutator may involve a cpDNA repair pathway.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ahne A, Muller-Derlich J, Merlos-Lange AM, Kanbay F, Wolf K, Lang BF (1988) Two distinct mechanisms for deletion in mitochondrial DNA of Schizosaccharomyces pombe mutator strains. J Mol Biol 202:725–734

    Google Scholar 

  • Backer J, Foury F (1985) Repair properties in yeast mitochondrial mutators. Curr Genet 10:7–13

    Google Scholar 

  • Börner T, Sears BB (1986) Plastome mutants. Mol Biol Rep 4:69–92

    Google Scholar 

  • Cella R, Iadarola P (1983) Characterization of carrot cell lines resistant to 5-methyltryptophan obtained by irradiating suspension cultures with UV light. Plant Sci Lett 29:327–337

    Google Scholar 

  • Chiu W-L, Johnson EM, Kaplan SA, Blasko K, Wolfson R, Sokalski MK, Sears BB (1990) Oenothera chloroplast DNA polymorphisms associated with plastome mutator activity. Mol Gen Genet 221:59–64

    Google Scholar 

  • Del Giudice L, Massardo DR, Manna F, Wolf K (1986) Isolation and characterization of a conditional mutant in Saccharomyces cerevisiae producing rho° peptites at the nonpermissive temperature. Curr Genet 121:201–204

    Google Scholar 

  • Epp M (1973) Nuclear gene-induced plastome mutations in Oenothera hookeri. I. Genetic analysis. Genetics 75:465–483

    Google Scholar 

  • Epp MD, Parthasarthy MV (1987) Nuclear gene-induced plastome mutations in Oenothera hookeri. II. Phenotype description with electron microscopy. Am J Bot 74:143–151

    Google Scholar 

  • Foury F, Kolodynski J (1983) Pif mutation blocks recombination between mitochondrial rho+ and rho genomes having tandemly arrayed repeat units in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 80:5345–5349

    Google Scholar 

  • Foury F, Van Dyck E (1985) A PIF-dependent recombinogenic signal in the mitochondrial DNA of yeast. EMBO J 4:3525–3530

    Google Scholar 

  • Genga A, Bianchi L, Foury F (1986) A nuclear mutant of Sacharomyces cerevisiae deficient in mitochondrial DNA replication and polymerase activity. J Biol Chem 261:9328–9332

    Google Scholar 

  • Hagemann RF (1982) Induction of plastome mutations by nitrosourea compounds. In: Edelman M, Hallick R, Chua N-H (eds) Methods in chloroplast molecular biology. Elsevier, Amsterdam, pp 119–127

    Google Scholar 

  • Hagemann RF (1986) A speical type of nucleus-plastid interaction: nuclear gene-induced plastome mutations. In: Akoyunoglou G, Senger H (eds) Regulation of chloroplast differentiation. Liss, NY, pp 455–466

    Google Scholar 

  • Harris EH (1989) The Chlamydomonas source book. Academic Press, San Diego, p 780

    Google Scholar 

  • Hosticka LP, Hanson MR (1984) Induction of plastid mutations in tomatoes by nitrosomethylurea. J Hered 75:242–246

    Google Scholar 

  • Ikenaga M, Mabuchi T (1966) Photoreactivation of endosperm mutations induced by ultraviolet light in maize. Radiat Bot 6:165–169

    Google Scholar 

  • Johnson EM, Schnabelrauch LS, Sears BB (1991) A plastome mutation affects processing of both chloroplast and nuclear DNA-encoded plastid proteins. Mol Gen Genet 225:106–112

    Google Scholar 

  • Kumura K, Sekiguchi M (1984) Identification of the uvrD gene product of Escherichia coli as DNA helicase II and its induction by DNA-damaging agents. J Biol Chem 259:1560–1565

    Google Scholar 

  • Lindahl T, Sedgwick B, Sekiguchi M, Nakabeppu Y (1988) Regulation and expression of the adaptive response to alkylating agents. Annu Rev Biochem 57:133–157

    Google Scholar 

  • Linne von Berg G (1990) Die Lokalisation der Gene für den Plastommutator (pm) und die Selbstinkompatibilität (Si) in Sippen der Subsektion Evoenothera. PhD Thesis, University of Düsseldorf, Federal Republic of Germany

    Google Scholar 

  • McCabe PF, Timmons AM, Dix PJ (1989) A simple procedure for the isolation of streptomycin-resistant plants in Solanaceae. Mol Gen Genet 216:132–137

    Google Scholar 

  • McLennan AG (1987) The repair of ultraviolet light-induced DNA damage in plant cells. Mutat Res 181:1–7

    Google Scholar 

  • Michaelis P (1969) Über Plastiden-Restitutionen (Rückmutatio-nen). Cytologia 34 (Suppl):1–115

    Google Scholar 

  • Nagata T, Takebe I (1971) Plating of isolated tobacco mesophyll protoplasts on agar medium. Planta 99:12–20

    Google Scholar 

  • Ohyama K, Pelcher LE, Gamborg OL (1974) The effects of ultraviolet irradiation on survival and on nucleic acids and protein synthesis in plant protoplasts. Radiat Bot 14:343–346

    Google Scholar 

  • Oppermann T, Hong T-H, Surzycki SJ (1989) Chloroplast and nuclear genomes of Chlamydomonas reinhardtii share homology with Escherichia coli genes for DNA replication, repair and transcription. Curr Genet 15:39–46

    Google Scholar 

  • Potrykus I (1970) Mutation and Rückmutation extrachromosomale vererbter Plastidenmerkmale von Petunia. Z Pflanzenzucht 63:24–40

    Google Scholar 

  • Redei GP, Plurad SB (1973) Hereditary structural alterations of plastids induced by a nuclear gene in Arabidopsis. Protoplasma 77:361–380

    Google Scholar 

  • Robberecht R, Caldwell MM (1978) Leaf epidermal transmittance of ultraviolet radiation and its implications for plant sensitivity to ultraviolet-radiation induced injury. Oecologia 32:277–287

    Google Scholar 

  • Sargentini NJ, Smith KC (1985) Spontaneous mutagenesis: the roles of DNA repair, replication, and recombination. Mutat Res 154:1–27

    Google Scholar 

  • Sears BB (1983) Genetics and evolution of the chloroplast. In: Gustafsson P (ed) Stadler Symposium vol 15, University of Missouri Press, Columbia, MO, pp 119–139

    Google Scholar 

  • Stubbe W, herrmann RG (1982) Selection and maintenance of plastome mutants and interspecific genome/plastome hybrids from Oenothera. In: Edelman M, Hallick R, Chua N-H (eds) Methods in chloroplast molecular biology. Elsevier, Amsterdam, pp 149–165

    Google Scholar 

  • Tevini M, Iwanzik W, Thoma U (1981) Some effects of enhanced UV-B irradiation on the growth and composition of plants. Planta 153:388–394

    Google Scholar 

  • Tilney-Bassett RAE (1975) Genetics of variegated plants. In: Birky CW Jr, Perlman PS, Byers TJ (eds) Ohio State University Press, Columbus, OH, pp 268–308

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by R.G. Herrmann

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sears, B.B., Sokalski, M.B. The Oenothera plastome mutator : effect of UV irradiation and nitroso-methyl urea on mutation frequencies. Molec. Gen. Genet. 229, 245–252 (1991). https://doi.org/10.1007/BF00272162

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00272162

Key words

Navigation