Cited by 225Plant tissue culture and regenerationEpigenetics and DNA MethylationPlant Genetic and Mutation Studies

Tissue Culture-Induced DNA Methylation Variation in Maize

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Kaeppler, S M, Phillips, R L·1993·Proceedings of the National Academy of Sciences

Abstract

Twenty-one progeny lines derived from tissue cultures of two embryo sources of maize inbred strain A188 were examined for DNA methylation changes. Total DNA was cut with the isoschizomers Hpa II and Msp I and probed with 18 single-copy Pst I genomic clones and two cDNA clones. Eight of these probes could detect both increases and decreases in methylation. With these probes 39% of the families were found to contain an altered methylation pattern. All changes represented a decrease in methylation. The other 12 probes could detect only increases in methylation; no methylation variation was seen with these probes. Fifteen percent of the methylation changes were homozygous in the original regenerated plant. Changes were stably inherited upon two generations of self-pollination. No sequence variation was observed in Msp I-digested DNA from the same 21 progeny lines. Certain probes detected methylation changes much more often than others. Our study provides evidence that demethylation occurs at a high frequency and could be an important cause of tissue culture-induced variation. Occurrence of the frequent homozygous alterations in original regenerated plants implies a non-random mutational mechanism.

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  • In Zea mays callus culture, no variation was observed.

    “No variation observed”

    From Somaclonal Variation and Clonal Fidelity in Commercial Micropropagation: Challenges and Perspectives (2025) · cites this paper as [100]

    The Results and Discussion report DNA methylation variation in maize lines derived from tissue culture, including altered bands in regenerant-derived families. The paper says noncultured controls were invariant; its findings do not support an unqualified claim that no variation was observed in cultured maize. (LLM, conf=0.90)

    Checked by a reasoning model — may be wrong.

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  • These methylation changes were stably inherited across two generations, suggesting demethylation as a major contributor to tissue culture-induced variation, with certain probes detecting methylation changes more frequently.

    “These changes were stably inherited across two generations, suggesting demethylation as a major contributor to tissue culture-induced variation, with certain probes detecting methylation changes more frequently [100].”
  • In Zea mays A188, altered DNA methylation patterns were found in 39% of progeny lines, primarily due to stable, heritable demethylation.

    “Altered DNA methylation stable, heritable demethylation. patterns were found in 39% of progeny lines, primarily due to”
  • In 21 maize progeny lines from tissue cultures of inbred strain A188, 39% of families had altered methylation patterns, all showing a decrease in methylation.

    “Moreover, a study on 21 maize progeny lines from tissue cultures of inbred strain A188 revealed 39% of families had altered methylation patterns, all showing a decrease in methylation.”

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References 15 · Cited by 225

Research works printed but not linked: 12

  1. Larkin, P. J. & Scowcroft, W. R. (1983) in Genetic Engineering of Plants: An Agricultural Perspective, eds. Kosuge, T., Meredith, C. P. & Holleander, A. (Plenum, New York), pp. 289-314.
  2. Rice, T. B. (1982) in Proceedings ofthe 37th Annual Corn and SorghumResearch Conference (Am. SeedTrade Assoc., Wash- ington, DC), pp. 148-162.
  3. Benzion, G. (1984) Dissertation (Univ. of Minnesota, Minne- apolis).
  4. Vasil, I. K. (Academic, New York), Vol. 3, pp. 435-448.
  5. Phillips, R. L., Kaeppler, S. M. & Peschke, V. M. (1990) in Proceedings of the Seventh International Congress on Plant Tissue and Cell Culture, eds.
  6. Nijkamp, H. J. J., Van Der Plas, L. H. W. & Van Aartrijk, J. (Kluwer, Dordrecht, The Neth- erlands), pp. 131-141.
  7. Schwartz, D. (1989) Proc. Natl. Acad. Sci. USA 86,2789-2793.
  8. Monk, M. (1990) Philos. Trans. R. Soc. London Ser. B 326, 299-312.
  9. Armstrong, C. A. (1986) Dissertation (Univ. of Minnesota, Minneapolis).
  10. Saghai-Maroof, M. A., Soliman, K. M., Jorgensen, R. A. & Allard, R. W. (1984) Proc. Natl. Acad. Sci. USA 81, 8014- 8018.
  11. Hall, G., Allen, G. C., Loer, D. S., Thompson, W. F. & Spiker, S. (1991) Proc. Natl. Acad. Sci. USA 88, 9320-9324.
  12. Compton, M. E. & Veilleux, R. E. (1991) Genome 34,810-817. Proc. Natl. Acad Sci. USA 90 (1993)

Authors
Kaeppler, S. M., & Phillips, R. L.
Affiliations
  • University of Minnesota (US)
  • University of Nebraska–Lincoln (US)
Venue
Proceedings of the National Academy of Sciences
Published
1993-10
Volume
90
Issue
19
Pages
8773-8776
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2073498816
Cited by
225
References
15
Citations by year
2026: 4 · 2025: 6 · 2024: 3 · 2023: 2 · 2022: 4 · 2021: 8 · 2020: 5 · 2019: 8 · 2018: 7 · 2017: 8 · 2016: 6 · 2015: 9 · 2014: 5 · 2013: 6 · 2012: 11
FWCI
1.42
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Agriculture
  • University of Minnesota
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant tissue culture and regeneration
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Genetic and Mutation Studies
Keywords
DNA methylation, demethylation, maize, embryo culture, cDNA clones, HpaII, MspI
MeSH terms
Base Sequence, Zea mays, DNA, Homozygote, Methylation, Seeds, Genetic Variation, Restriction Mapping, Culture Techniques

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