The Arabidopsis dwarf1 Mutant Is Defective in the Conversion of 24-Methylenecholesterol to Campesterol in Brassinosteroid Biosynthesis

• Published in: Plant physiology (Bethesda) 1999-03, Vol.119 (3), p.897-907
• Main Authors: Choe, Sunghwa, Dilkes, Brian P., Gregory, Brian D., Ross, Amanda S., Heng Yuan, Noguchi, Takahiro, Fujioka, Shozo, Takatsuto, Suguru, Tanaka, Atsushi, Yoshida, Shigeo, Tax, Frans E., Feldmann, Kenneth A.
• Format: Article
• Language: English
• Subjects: Agronomy. Soil science and plant productions; Alleles; Amino Acid Sequence; Amino acids; Arabidopsis; Arabidopsis - genetics; Arabidopsis - growth & development; Arabidopsis - metabolism; Base Sequence; Biological and medical sciences; Biosynthesis; Brassinosteroids; Cholestanols - metabolism; Cholesterol - analogs & derivatives; Cholesterol - biosynthesis; Cholesterol - metabolism; Complementary DNA; DNA; DNA Primers - genetics; Economic plant physiology; Enzymes; Fundamental and applied biological sciences. Psychology; Genes, Plant; Genetic mutation; Growth and development; Growth regulators; Inflorescences; Metabolism; Molecular Genetics and Genomics; Molecular Sequence Data; Mutation; Phenotypes; Phytosterols; Plant physiology and development; Plant Proteins - genetics; Plants; Sequence Homology, Amino Acid; Steroids, Heterocyclic - metabolism
• ISSN: 0032-0889; 1532-2548
• DOI: 10.1104/pp.119.3.897

Since the isolation and characterization of dwarf1-1 (dwf1-1) from a T-DNA insertion mutant population, phenotypically similar mutants, including deetiolated2 (det2), constitutive photomorphogenesis and dwarfism (cpd), brassinosteroid insensitive1 (bri1), and dwf4, have been reported to be defective in either the biosynthesis or the perception of brassinosteroids. We present further characterization of dwf1-1 and additional dwf1 alleles. Feeding tests with brassinosteroid-biosynthetic intermediates revealed that dwf1 can be rescued by 22α-hydroxycampesterol and downstream intermediates in the brassinosteroid pathway. Analysis of the endogenous levels of brassinosteroid intermediates showed that 24-methylenecholesterol in dwf1 accumulates to 12 times the level of the wild type, whereas the level of campesterol is greatly diminished, indicating that the defective step is in C-24 reduction. Furthermore, the deduced amino acid sequence of DWF1 shows significant similarity to a flavin adenine dinucleotide-binding domain conserved in various oxidoreductases, suggesting an enzymatic role for DWF1. In support of this, 7 of 10 dwf1 mutations directly affected the flavin adenine dinucleotide-binding domain. Our molecular characterization of dwf1 alleles, together with our biochemical data, suggest that the biosynthetic defect in dwf1 results in reduced synthesis of bioactive brassinosteroids, causing dwarfism.