Structure-Activity Relationship Studies of Strigolactone-Related Molecules for Branching Inhibition in Garden Pea: Molecule Design for Shoot Branching

Author:

Boyer François-Didier1,de Saint Germain Alexandre1,Pillot Jean-Paul1,Pouvreau Jean-Bernard1,Chen Victor Xiao1,Ramos Suzanne1,Stévenin Arnaud1,Simier Philippe1,Delavault Philippe1,Beau Jean-Marie1,Rameau Catherine1

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, Unité Propre de Recherche 2301 Centre National de la Recherche Scientifique, F–91198 Gif-sur-Yvette cedex, France (F.-D.B., V.X.C., S.R., A.S., J.-M.B.) Unité Mixte de Recherche 1318 INRA-AgroParisTech, Institut Jean-Pierre Bourgin, F–78000 Versailles, France (A.d.S.G., J.-P.P., C.R.); and L'Université Nantes Angers Le Mans

Abstract

Abstract Initially known for their role in the rhizosphere in stimulating the seed germination of parasitic weeds such as the Striga and Orobanche species, and later as host recognition signals for arbuscular mycorrhizal fungi, strigolactones (SLs) were recently rediscovered as a new class of plant hormones involved in the control of shoot branching in plants. Herein, we report the synthesis of new SL analogs and, to our knowledge, the first study of SL structure-activity relationships for their hormonal activity in garden pea (Pisum sativum). Comparisons with their action for the germination of broomrape (Phelipanche ramosa) are also presented. The pea rms1  SL-deficient mutant was used in a SL bioassay based on axillary bud length after direct SL application on the bud. This assay was compared with an assay where SLs were fed via the roots using hydroponics and with a molecular assay in which transcript levels of BRANCHED1, the pea homolog of the maize TEOSINTE BRANCHED1 gene were quantified in axillary buds only 6 h after application of SLs. We have demonstrated that the presence of a Michael acceptor and a methylbutenolide or dimethylbutenolide motif in the same molecule is essential. It was established that the more active analog 23 with a dimethylbutenolide as the D-ring could be used to control the plant architecture without strongly favoring the germination of P. ramosa seeds. Bold numerals refer to numbers of compounds.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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