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

被引:151
作者
Boyer, Francois-Didier [1 ]
Germain, Alexandre de Saint [2 ]
Pillot, Jean-Paul [2 ]
Pouvreau, Jean-Bernard [3 ]
Chen, Victor Xiao [1 ]
Ramos, Suzanne [1 ]
Stevenin, Arnaud [1 ]
Simier, Philippe [3 ]
Delavault, Philippe [3 ]
Beau, Jean-Marie [1 ]
Rameau, Catherine [2 ]
机构
[1] Ctr Natl Rech Sci, Ctr Rech Gif, Inst Chim Subst Nat, Unite Propre Rech 2301, F-91198 Gif Sur Yvette, France
[2] Inst Jean Pierre Bourgin, INRA AgroParisTech, Unite Mixte Rech 1318, F-78000 Versailles, France
[3] Univ Nantes Angers Le Mans, Lab Biol & Pathol Vegetales, Inst Federatif Rech Qual & Sante Vegetal 149, EA 1157, F-44322 Nantes 3, France
关键词
ROOT PARASITIC PLANTS; ARBUSCULAR MYCORRHIZAL FUNGI; STRIGA-GESNERIOIDES SEEDS; GERMINATION STIMULANTS; BIOLOGICAL EVALUATION; ACTS DOWNSTREAM; BUD OUTGROWTH; ANALOG GR24; LUTEA LOUR; AM FUNGI;
D O I
10.1104/pp.112.195826
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:1524 / 1544
页数:21
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