Abstract

Brassinosteroids are steroidal hormones essential for the growth and development of plants. Brassinolide, the most biologically active brassinosteroid, has a seven-membered lactone ring that is formed by a Baeyer-Villiger oxidation of its immediate precursor castasterone. Despite its potential key role in controlling plant development, brassinolide synthase has not been identified. Previous work has shown that the formation of castasterone from 6-deoxocastasterone is catalyzed by members of the CYP85A family of cytochrome P-450 monooxygenases. A null mutation in the tomato Dwarf (CYP85A1) gene, extreme dwarf (d(x)), causes severe dwarfism due to brassinosteroid deficiency, but the d(x) mutant still produces fruits. Here, we show that d(x) fruits contain brassinolide at a higher level than wild-type fruits and that a new CYP85A gene, CYP85A3, is preferentially expressed in tomato fruits. Tomato CYP85A3 catalyzed the Baeyer-Villiger oxidation to produce brassinolide from castasterone in yeast, in addition to the conversion of 6-deoxocastasterone to castasterone. We also show that Arabidopsis CYP85A2, which was initially characterized as castasterone synthase, also has brassinolide synthase activity. Exogenous application of castasterone and brassinolide to the Arabidopsis cyp85a1/cyp85a2 double mutant suggests that castasterone can function as an active brassinosteroid but that its conversion into brassinolide is necessary for normal vegetative development in Arabidopsis. We postulate that castasterone is the major active brassinosteroid during vegetative growth in tomato, whereas brassinolide may play an organ-specific role in fruit development in this species.

Highlights

  • Brassinosteroids are steroidal hormones essential for the growth and development of plants

  • We show that Arabidopsis CYP85A2, which was initially characterized as castasterone synthase, has brassinolide synthase activity

  • Using heterologous expression in yeast, we have demonstrated that at least one of the CYP85A family members in tomato and Arabidopsis is able to catalyze the BaeyerVilliger type oxidation for the production of BL (Fig. 4)

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Summary

EXPERIMENTAL PROCEDURES

Plant Materials—Near isogenic tomato (L. esculentum) lines of Ailsa Craig carrying either D (GCR 358) or the dx (GCR 567) allele were originally obtained from J. Yeast Functional Assay—The CYP85A1 and CYP85A2 cDNAs of Arabidopsis were amplified from a single-strand cDNA library made from young siliques (ϳ3 mm in length) of Arabidopsis using primer pairs: 85A1-F1 (BamHI site at the initiation codon) and 85A1-R1 (KpnI site at the stop codon) and 85A2-F1 (BamHI site at the initiation codon) and 85A2-R1 (KpnI site at the stop codon), respectively. These PCR products were cloned using TOPO TA Cloning (Invitrogen) and checked to ensure that no PCR errors were introduced. The latter phase was evaporated to dryness and derivatized with pyridine containing methaneboronic acid (2 mg mlϪ1) prior to GC-MS analysis using an Automass (JEOL) plus 6890N (Agilent Technologies) instrument equipped with a DB-1 column (J & W Scientific; 0.25 mm ϫ 15 m; 0.25-␮m film thickness) under the same conditions as Ref. 8

RESULTS
NDa 426
DISCUSSION
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