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Molecular basis for three-dimensional elaboration of the Aquilegia petal spur

  • Levi Yant
  • , Silvio Collani
  • , Joshua Puzey
  • , Clara Levy
  • , Elena M. Kramer

Research output: Contribution to journalArticlepeer-review

Abstract

By enforcing specific pollinator interactions, Aquilegia petal nectar spurs maintain reproductive isolation between species. Spur development is the result of three-dimensional elaboration from a comparatively two-dimensional primor-dium. Initiated by localized, oriented cell divisions surrounding the incipient nectary, this process creates a pouch that is extended by anisotropic cell elongation. We hypothesized that the development of this evolutionary novelty could be promoted by non-mutually exclusive factors, including (i) prolonged, KNOX-dependent cell fate indeterminacy, (ii) localized organ sculpting and/or (iii) redeployment of hormone-signalling modules. Using cell division markers to guide transcriptome analysis of microdissected spur tissue, we present candidate mechanisms underlying spur outgrowth. We see dynamic expression of factors controlling cell proliferation and hormone signalling, but no evidence of contribution from indeterminacy factors. Tran-scriptome dynamics point to a novel recruitment event in which auxin-related factors that normally functionat the organ margin were co-optedto this central structure. Functional perturbation of the transition between cell division and expansion reveals an unexpected asymmetric component ofspur development. These findings indicate that the production of this three-dimensional form is an example of organ sculpting via localized cell division with novel contributions from hormone signalling, rather than a product of prolonged indeterminacy.

Original languageEnglish
Article number20142778
JournalProceedings of the Royal Society B: Biological Sciences
Volume282
Issue number1803
DOIs
Publication statusPublished - 2015
Externally publishedYes

Keywords

  • Aquilegia
  • Gene expression
  • Hormones
  • Organ shape
  • TCP4
  • Virus-induced gene silencing

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