Itoh Hironori, Tatsumi Tomoko, Sakamoto Tomoaki, Otomo Kazuko, Toyomasu Tomonobu, Kitano Hidemi, Ashikari Motoyuki, Ichihara Shigeyuki, Matsuoka Makoto
Bioscience and Biotechnology Center, Nagoya University, Nagoya, Aichi 464-8601, Japan.
Plant Mol Biol. 2004 Mar;54(4):533-47. doi: 10.1023/B:PLAN.0000038261.21060.47.
A rice (Oryza sativa L.) semi-dwarf cultivar, Tan-Ginbozu (d35Tan-Ginbozu), contributed to the increase in crop productivity in Japan in the 1950s. Previous studies suggested that the semi-dwarf stature of d35Tan-Ginbozu is caused by a defective early step of gibberellin biosynthesis, which is catalyzed by ent-kaurene oxidase (KO). To study the molecular characteristics of d35Tan-Ginbozu, we isolated 5 KO-like (KOL) genes from the rice genome, which encoded proteins highly homologous to Arabidopsis and pumpkin KOs. The genes (OsKOL1 to 5) were arranged as tandem repeats in the same direction within a 120 kb sequence. Expression analysis revealed that OsKOL2 and OsKOL4 were actively transcribed in various organs, while OsKOL1 and OsKOL5 were expressed only at low levels; OsKOL3 may be a pseudogene. Sequence analysis and complementation experiments demonstrated that OsKOL2 corresponds to D35. Homozygote with null alleles of D35 showed a severe dwarf phenotype; therefore, d35Tan-Ginbozu is a weak allele of D35. Introduction of OsKOL4 into d35Tan-Ginbozu did not rescue its dwarf phenotype, indicating that OsKOL4 is not involved in GA biosynthesis. OsKOL4 and OsKOL5 are likely to take part in phytoalexin biosynthesis, because their expression was promoted by UV irradiation and/or elicitor treatment. Comparing d35Tan-Ginbozu with other high yielding cultivars, we discuss strategies to produce culm architectures suitable for high crop yield by decreasing GA levels.
一个水稻(Oryza sativa L.)半矮秆品种“淡金坊主(d35淡金坊主)”,在20世纪50年代推动了日本作物产量的提高。先前的研究表明,d35淡金坊主的半矮秆株型是由赤霉素生物合成早期步骤缺陷导致的,该步骤由内根-贝壳杉烯氧化酶(KO)催化。为了研究d35淡金坊主的分子特征,我们从水稻基因组中分离出5个类KO(KOL)基因,它们编码的蛋白质与拟南芥和南瓜的KO高度同源。这些基因(OsKOL1至5)在120 kb序列内以相同方向串联排列。表达分析表明,OsKOL2和OsKOL4在各个器官中活跃转录,而OsKOL1和OsKOL5仅低水平表达;OsKOL3可能是一个假基因。序列分析和互补实验表明,OsKOL2对应于D35。D35无效等位基因的纯合子表现出严重的矮化表型;因此,d35淡金坊主是D35的一个弱等位基因。将OsKOL4导入d35淡金坊主并不能挽救其矮化表型,这表明OsKOL4不参与赤霉素生物合成。OsKOL4和OsKOL5可能参与植保素生物合成,因为它们的表达受紫外线照射和/或激发子处理的促进。通过比较d35淡金坊主与其他高产品种,我们讨论了通过降低赤霉素水平来培育适合高作物产量的茎秆结构的策略。