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An epigenetic mutation responsible for natural variation in floral symmetry

Author

Listed:
  • Pilar Cubas

    (John Innes Centre
    Centro Nacional de Biotecnologia Campus de la Universidad Autónoma de Madrid, Cantoblanco)

  • Coral Vincent

    (John Innes Centre)

  • Enrico Coen

    (John Innes Centre)

Abstract

Although there have been many molecular studies of morphological mutants generated in the laboratory, it is unclear how these are related to mutants in natural populations, where the constraints of natural selection and breeding structure are quite different. Here we characterize a naturally occurring mutant of Linaria vulgaris, originally described more than 250 years ago by Linnaeus1,2,3, in which the fundamental symmetry of the flower is changed from bilateral to radial. We show that the mutant carries a defect in Lcyc, a homologue of the cycloidea gene which controls dorsoventral asymmetry in Antirrhinum4. The Lcyc gene is extensively methylated and transcriptionally silent in the mutant. This modification is heritable and co-segregates with the mutant phenotype. Occasionally the mutant reverts phenotypically during somatic development, correlating with demethylation of Lcyc and restoration of gene expression. It is surprising that the first natural morphological mutant to be characterized should trace to methylation, given the rarity of this mutational mechanism in the laboratory. This indicates that epigenetic mutations may play a more significant role in evolution than has hitherto been suspected.

Suggested Citation

  • Pilar Cubas & Coral Vincent & Enrico Coen, 1999. "An epigenetic mutation responsible for natural variation in floral symmetry," Nature, Nature, vol. 401(6749), pages 157-161, September.
  • Handle: RePEc:nat:nature:v:401:y:1999:i:6749:d:10.1038_43657
    DOI: 10.1038/43657
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    Cited by:

    1. Jie Liu & Xuehua Zhong, 2024. "Epiallelic variation of non-coding RNA genes and their phenotypic consequences," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    2. Peter Sarkies & Jennifer Westoby & Rebecca Mary Kilner & Rahia Mashoodh, 2024. "Gene body methylation evolves during the sustained loss of parental care in the burying beetle," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    3. Carja, Oana & Liberman, Uri & Feldman, Marcus W., 2013. "Evolution with stochastic fitnesses: A role for recombination," Theoretical Population Biology, Elsevier, vol. 86(C), pages 29-42.
    4. Yinwen Zhang & Hosung Jang & Rui Xiao & Ioanna Kakoulidou & Robert S. Piecyk & Frank Johannes & Robert J. Schmitz, 2021. "Heterochromatin is a quantitative trait associated with spontaneous epiallele formation," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    5. Grégoire Vernaz & Milan Malinsky & Hannes Svardal & Mingliu Du & Alexandra M. Tyers & M. Emília Santos & Richard Durbin & Martin J. Genner & George F. Turner & Eric A. Miska, 2021. "Mapping epigenetic divergence in the massive radiation of Lake Malawi cichlid fishes," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    6. Geoghegan, Jemma L. & Spencer, Hamish G., 2013. "Exploring epiallele stability in a population-epigenetic model," Theoretical Population Biology, Elsevier, vol. 83(C), pages 136-144.

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