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Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses.

Cuong Nguyen HuuChristian KappelBarbara KellerAdrien SicardYumiko TakebayashiHolger BreuningerMichael D NowakIsabel BäurleAxel HimmelbachMichael BurkartThomas Ebbing-LohausHitoshi SakakibaraLothar AltschmiedElena ContiMichael Lenhard
Published in: eLife (2016)
Heterostyly is a wide-spread floral adaptation to promote outbreeding, yet its genetic basis and evolutionary origin remain poorly understood. In Primula (primroses), heterostyly is controlled by the S-locus supergene that determines the reciprocal arrangement of reproductive organs and incompatibility between the two morphs. However, the identities of the component genes remain unknown. Here, we identify the Primula CYP734A50 gene, encoding a putative brassinosteroid-degrading enzyme, as the G locus that determines the style-length dimorphism. CYP734A50 is only present on the short-styled S-morph haplotype, it is specifically expressed in S-morph styles, and its loss or inactivation leads to long styles. The gene arose by a duplication specific to the Primulaceae lineage and shows an accelerated rate of molecular evolution. Thus, our results provide a mechanistic explanation for the Primula style-length dimorphism and begin to shed light on the evolution of the S-locus as a prime model for a complex plant supergene.
Keyphrases
  • genome wide
  • copy number
  • genome wide identification
  • dna methylation
  • genome wide association study
  • genome wide analysis
  • transcription factor
  • gene expression
  • bioinformatics analysis
  • plant growth