Isolation and characterization of a rice dwarf mutant with a defect in brassinosteroid biosynthesis

被引:248
作者
Mori, M [1 ]
Nomura, T
Ooka, H
Ishizaka, M
Yokota, T
Sugimoto, K
Okabe, K
Kajiwara, H
Satoh, K
Yamamoto, K
Hirochika, H
Kikuchi, S
机构
[1] Natl Inst Agrobiol Sci, Dept Mol Genet, Tsukuba, Ibaraki 3058602, Japan
[2] Natl Inst Agrobiol Sci, Dept Biochem, Tsukuba, Ibaraki 3058602, Japan
[3] Teikyo Univ, Dept Biosci, Utsunomiya, Tochigi 3208551, Japan
[4] Nagaoka Univ Technol, Nagaoka, Niigata 9402137, Japan
[5] Natl Inst Agroenvironm Sci, Chem Anal Res Ctr, Tsukuba, Ibaraki 3058604, Japan
关键词
D O I
10.1104/pp.007179
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We have isolated a new recessive dwarf mutant of rice (Oryza saliva L. cv Nipponbare). Under normal growth conditions, the mutant has very short leaf sheaths; has short, curled, and frizzled leaf blades; has few tillers; and is sterile. Longitudinal sections of the leaf sheaths revealed that the cell length along the longitudinal axis is reduced, which explains the short leaf sheaths. Transverse sections of the leaf blades revealed enlargement of the motor cells along the dorsal-ventral axis, which explains the curled and frizzled leaf blades. In addition, the number of crown roots was smaller and the growth of branch roots was weaker than those in the wild-type plant. Because exogenously supplied brassinolide considerably restored the normal phenotypes, we designated the mutant brassinosteroid-dependent 1 (brd1). Further, under darkness, brd1 showed constitutive photomorphogenesis. Quantitative analyses of endogenous sterols and brassinosteroids (BRs) indicated that BR-6-oxidase, a BR biosynthesis enzyme, would be defective. In fact, a 0.2-kb deletion was detected in the genomic region of OsBR6ox (a rice BR-6-oxidase gene) in the brd1 mutant. These results indicate that BRs are involved in many morphological and physiological processes in rice, including the elongation and unrolling of leaves, development of tillers, skotomorphogenesis, root differentiation, and reproductive growth, and that the defect of BR-6-oxidase caused the brd1 phenotype.
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页码:1152 / 1161
页数:10
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