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A plant-based chemical genomics screen for the identification of flowering inducers.
Fiers, Martijn; Hoogenboom, Jorin; Brunazzi, Alice; Wennekes, Tom; Angenent, Gerco C; Immink, Richard G H.
Afiliación
  • Fiers M; Bioscience, Wageningen University and Research, 6700 AP Wageningen, The Netherlands.
  • Hoogenboom J; Laboratory of Molecular Biology, Wageningen University and Research, 6708 PB Wageningen, The Netherlands.
  • Brunazzi A; Laboratory of Organic Chemistry, Wageningen University and Research, 6708 WE Wageningen, The Netherlands.
  • Wennekes T; Bioscience, Wageningen University and Research, 6700 AP Wageningen, The Netherlands.
  • Angenent GC; Laboratory of Organic Chemistry, Wageningen University and Research, 6708 WE Wageningen, The Netherlands.
  • Immink RGH; Department of Chemical Biology and Drug Discovery, Utrecht Institute for Pharmaceutical Sciences and Bijvoet Center for Biomolecular Research, Utrecht University, 3584 CH Utrecht, The Netherlands.
Plant Methods ; 13: 78, 2017.
Article en En | MEDLINE | ID: mdl-29026434
ABSTRACT

BACKGROUND:

Floral timing is a carefully regulated process, in which the plant determines the optimal moment to switch from the vegetative to reproductive phase. While there are numerous genes known that control flowering time, little information is available on chemical compounds that are able to influence this process. We aimed to discover novel compounds that are able to induce flowering in the model plant Arabidopsis. For this purpose we developed a plant-based screening platform that can be used in a chemical genomics study.

RESULTS:

Here we describe the set-up of the screening platform and various issues and pitfalls that need to be addressed in order to perform a chemical genomics screening on Arabidopsis plantlets. We describe the choice for a molecular marker, in combination with a sensitive reporter that's active in plants and is sufficiently sensitive for detection. In this particular screen, the firefly Luciferase marker was used, fused to the regulatory sequences of the floral meristem identity gene APETALA1 (AP1), which is an early marker for flowering. Using this screening platform almost 9000 compounds were screened, in triplicate, in 96-well plates at a concentration of 25 µM. One of the identified potential flowering inducing compounds was studied in more detail and named Flowering1 (F1). F1 turned out to be an analogue of the plant hormone Salicylic acid (SA) and appeared to be more potent than SA in the induction of flowering. The effect could be confirmed by watering Arabidopsis plants with SA or F1, in which F1 gave a significant reduction in time to flowering in comparison to SA treatment or the control.

CONCLUSIONS:

In this study a chemical genomics screening platform was developed to discover compounds that can induce flowering in Arabidopsis. This platform was used successfully, to identify a compound that can speed-up flowering in Arabidopsis.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Plant Methods Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Plant Methods Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos