An epigenetic mutation responsible for natural variation in floral symmetry

Nature. 1999 Sep 9;401(6749):157-61. doi: 10.1038/43657.

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 Linnaeus, 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 Antirrhinum. 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • DNA Methylation
  • DNA, Plant
  • DNA-Binding Proteins
  • Genes, Plant
  • Magnoliopsida / genetics*
  • Magnoliopsida / physiology
  • Magnoliopsida / ultrastructure
  • Molecular Sequence Data
  • Mutation*
  • Plant Proteins / genetics*
  • Plant Proteins / physiology
  • Plant Structures / physiology
  • Plant Structures / ultrastructure
  • Polymorphism, Restriction Fragment Length
  • Transcription Factors

Substances

  • DNA, Plant
  • DNA-Binding Proteins
  • Plant Proteins
  • Transcription Factors
  • cycloidea protein, Antirrhinum

Associated data

  • GENBANK/AF161252