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A role for brassinosteroid signalling in decision-making processes in the Arabidopsis seedling.

Nils KalbfußAlexander StrohmayrMarcel KegelLien LeFriederike Grosse-HolzBarbara BrunschweigerKatharina StöcklChristian WieseCarina FrankeCaroline SchiestlSophia PremShuyao ShaKatrin Franz-OberdorfJuliane HafermannMarc ThieméEva FacherWojciech PalubickiCordelia BolleFarhah F Assaad
Published in: PLoS genetics (2022)
Plants often adapt to adverse conditions via differential growth, whereby limited resources are discriminately allocated to optimize the growth of one organ at the expense of another. Little is known about the decision-making processes that underly differential growth. In this study, we developed a screen to identify decision making mutants by deploying two tools that have been used in decision theory: a well-defined yet limited budget, as well as conflict-of-interest scenarios. A forward genetic screen that combined light and water withdrawal was carried out. This identified BRASSINOSTEROID INSENSITIVE 2 (BIN2) alleles as decision mutants with "confused" phenotypes. An assessment of organ and cell length suggested that hypocotyl elongation occurred predominantly via cellular elongation. In contrast, root growth appeared to be regulated by a combination of cell division and cell elongation or exit from the meristem. Gain- or loss- of function bin2 mutants were most severely impaired in their ability to adjust cell geometry in the hypocotyl or cell elongation as a function of distance from the quiescent centre in the root tips. This study describes a novel paradigm for root growth under limiting conditions, which depends not only on hypocotyl-versus-root trade-offs in the allocation of limited resources, but also on an ability to deploy different strategies for root growth in response to multiple stress conditions.
Keyphrases
  • decision making
  • single cell
  • cell therapy
  • magnetic resonance imaging
  • transcription factor
  • computed tomography
  • emergency department
  • climate change
  • dna methylation
  • mesenchymal stem cells
  • drug induced
  • wild type