2012
DOI: 10.4236/ajps.2012.312208
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New Alleles of Rice <i>ebisu dwarf</i> (<i>d</i>2) Mutant Show both Brassinosteroid-Deficient and -Insensitive Phenotypes

Abstract: ABSTRACTebisu dwarf (d2) is a mutant caused by mutation in a rice brassinosteroid biosynthetic enzyme gene, CYP90D2/D2, thereby conferring a brassinosteroid-deficient dwarf phenotype. Three newly isolated d2 alleles derived from a Nipponbare mutant library (d2-3, d2-4, and d2-6) produced more severe dwarf phenotypes than the previously characterized null allele from a Taichung 65 mutant library, d2-1. Linkage analysis and a complementation test clearly indicated that the mutant phenotypes in d2-6 were caused b… Show more

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Cited by 5 publications
(9 citation statements)
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“…2B). 31 We also confirmed the expression levels of three brassinosteroid-related genes, BU1, CYP85A1, and CYP734A2. BU1 is a primary brassinosteroid-responsive gene, and positively regulated by brassinosteroid treatment.…”
Section: Genome-wide Gene Expression Profiling Of Elf1-1supporting
confidence: 71%
“…2B). 31 We also confirmed the expression levels of three brassinosteroid-related genes, BU1, CYP85A1, and CYP734A2. BU1 is a primary brassinosteroid-responsive gene, and positively regulated by brassinosteroid treatment.…”
Section: Genome-wide Gene Expression Profiling Of Elf1-1supporting
confidence: 71%
“…Interestingly, the level of CYP85A1 mRNA in untreated d2-6 was lower than that of Nipponbare (about 85%), and was further decreased by brassinolide treatment (Figure 6(b)). Because the bioactive brassinosteroid castasterone accumulated in d2-6 mutant [30], we hypothesize that the expression of CYP85A1 may also be regulated directly by its catalytic product, castasterone. On the other hand, the level of CYP85A1 mRNA in d61-1N was 1.3 times that of wild-type Nipponbare and was not affected by brassinolide treatment (Figure 6(b)).…”
Section: Genetic Background Influences Brassinosteroid-related Mutantmentioning
confidence: 99%
“…CYP90D2/ D2 encodes a cytochrome P450 monooxygenase that functions in brassinosteroid C-23 hydroxylase [7]. We have isolated three new d2 alleles derived from a Nipponbare mutant library (d2-3, d2-4, and d2-6), and showed that they produced more severe dwarf phenotypes in the Nipponbare genetic background than did d2-1, a previously characterized null allele from a Taichung 65 mutant library [28], produced in the Taichung 65 genetic background [30]. The phenotype of Taichung 65-derived null allele d2-1 was semi-dwarf: plants reached ~55% (about 60 cm) of the total culm length of wild-type Taichung 65 (about 110 cm; Figures 5(a), (b) and (e)).…”
Section: Different Background-dependent Abnormal Phenotypes Were Alsomentioning
confidence: 99%
“…of d61, 13 which is caused by mutations in the brassinosteroid receptor gene OsBRI1, and another 3 were alleles of d2, 16 which is caused by mutations in the brassinosteroid biosynthetic enzyme gene CYP90D2/D2. The remaining mutant, elf1-1, was not an allele of the previously identified brassinosteroid-related mutants, so we further characterized this mutant.…”
Section: Elf1-1 Showed Brassinosteroid-insensitive Phenotypesmentioning
confidence: 99%
“…This mutant also had a short-grain phenotype similar to that observed for recently identified d61 and brassinosteroid-deficient d2 alleles. 13,16 elf1-1 also showed various brassinosteroid-related phenotypes including increased levels of an endogenous bioactive brassinosteroid; therefore, we hypothesized that elf1 mutants have defects in novel brassinosteroid signaling components. The ELF1 gene encodes a U-box-containing E3 ubiquitin ligase, and was found to be identical to the recently identified Taihu Dwarf1 (TUD1) gene.…”
Section: Introductionmentioning
confidence: 99%