Oh Keimei, Matsumoto Tadashi, Yamagami Ayumi, Ogawa Atushi, Yamada Kazuhiro, Suzuki Ryuichiro, Sawada Takayuki, Fujioka Shozo, Yoshizawa Yuko, Nakano Takeshi
Department of Biotechnology, Faculty of Bioresource Sciences, Akita Prefectural University, Shimoshinjo Nakano, Akita, Japan.
Antibiotics laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama, Japan.
PLoS One. 2015 Mar 20;10(3):e0120812. doi: 10.1371/journal.pone.0120812. eCollection 2015.
Plant hormone brassinosteroids (BRs) are a group of polyhydroxylated steroids that play critical roles in regulating broad aspects of plant growth and development. The structural diversity of BRs is generated by the action of several groups of P450s. Brassinazole is a specific inhibitor of C-22 hydroxylase (CYP90B1) in BR biosynthesis, and the application use of brassinazole has emerged as an effective way of complementing BR-deficient mutants to elucidate the functions of BRs. In this article, we report a new triazole-type BR biosynthesis inhibitor, YCZ-18. Quantitative analysis the endogenous levels of BRs in Arabidopsis indicated that YCZ-18 significantly decreased the BR contents in plant tissues. Assessment of the binding affinity of YCZ-18to purified recombinant CYP90D1 indicated that YCZ-18 induced a typical type II binding spectrum with a Kd value of approximately 0.79 μM. Analysis of the mechanisms underlying the dwarf phenotype associated with YCZ-18 treatment of Arabidopsis indicated that the chemically induced dwarf phenotype was caused by a failure of cell elongation. Moreover, dissecting the effect of YCZ-18 on the induction or down regulation of genes responsive to BRs indicated that YCZ-18 regulated the expression of genes responsible for BRs deficiency in Arabidopsis. These findings indicate that YCZ-18 is a potent BR biosynthesis inhibitor and has a new target site, C23-hydroxylation in BR biosynthesis. Application of YCZ-18 will be a good starting point for further elucidation of the detailed mechanism of BR biosynthesis and its regulation.
植物激素油菜素甾醇(BRs)是一类多羟基类固醇,在调节植物生长发育的广泛过程中发挥着关键作用。BRs的结构多样性是由几组细胞色素P450的作用产生的。油菜素唑是BR生物合成中C-22羟化酶(CYP90B1)的特异性抑制剂,油菜素唑的应用已成为补充BR缺陷突变体以阐明BR功能的有效方法。在本文中,我们报道了一种新型三唑类BR生物合成抑制剂YCZ-18。对拟南芥中BRs的内源水平进行定量分析表明,YCZ-18显著降低了植物组织中的BR含量。评估YCZ-18与纯化的重组CYP90D1的结合亲和力表明,YCZ-18诱导了典型的II型结合光谱,Kd值约为0.79μM。对与YCZ-18处理拟南芥相关的矮化表型的机制分析表明,化学诱导的矮化表型是由细胞伸长失败引起的。此外,剖析YCZ-18对BR响应基因的诱导或下调作用表明,YCZ-18调节了拟南芥中负责BR缺乏的基因的表达。这些发现表明,YCZ-18是一种有效的BR生物合成抑制剂,并且具有一个新的靶位点,即BR生物合成中的C23羟基化。YCZ-18的应用将是进一步阐明BR生物合成及其调控详细机制的良好起点。