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Function and molecular regulation of DWARF1 as a C-24 reductase in brassinosteroid biosynthesis in Arabidopsis

机译:拟拟拟合中芸苔类化合物生物合成中的幼达的矮化功能和分子调节

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DWARF1 functions as a brassinosteroid C-24 reductase that converts 24-methylene brassinosteroids to 24-methyl brassinosteroids to regulate the endogenous level of an active brassinosteroid, castasterone, to control growth and development in Arabidopsis.DWARF1 (DWF1) is a sterol C-24 reductase that catalyses the conversion of 24-methylenecholesterol (24-MCHR) to campesterol (CR) in Arabidopsis. A loss-of-function mutant, dwf1, showed similar phenotypic abnormalities to brassinosteroid (BR)-deficient mutants. These abnormalities were reversed in the wild-type phenotype by exogenous application of castasterone (CS) and brassinolide (BL), but not dolichosterone (DS). Accumulation of DS and decreased CS were found in quantitative analysis of endogenous BRs in dwf1. The enzyme solution prepared from dwf1 was unable to convert 6-deoxoDS to 6-deoxoCS and DS to CS, as seen in either wild-type or 35S:DWF1 transgenic plants. This suggests that DWF1 has enzyme activity not only for a sterol C-24 reductase, but also for a BR C-24 reductase that catalyses C-24 reduction of 6-deoxoDS to 6-deoxoCS and of DS to CS in Arabidopsis. Overexpression of DWF1 in a BR-deficient mutant (det2 35S:DWF1) clearly rescued abnormalities found in det2, indicating that DWF1 functions in biosynthesis of active BRs in Arabidopsis. Expression of DWF1 is down-regulated by application of CS and BL and in a BR-dominant mutant, bes1-D. E-boxes in the putative promoter region of DWF1 directly bind to a BR transcription factor, BES1, implying that DWF1 expression is feedback-regulated by BR signaling via BES1. Overall, biosynthesis of 24-methylene BR is an alternative route for generating CS, which is mediated and regulated by DWF1 in Arabidopsis.
机译:Dwarf1用作芸苔类化合物C-24还原酶,其将24-亚甲基芸苔类固醇转化为24-甲基芸苔类固醇,以调节活性芸苔类固醇的内源水平,以控制拟南芥的生长和发育.DWARF1(DWF1)是甾醇C-24还原酶将24-甲基金属石(24-甲基)转化为拟南芥(CR)的转化为拟南芥。功能突变突变体DWF1显示出与芸苔类固醇(BR)的突变体相似的表型异常。这些异常通过外源性施用Castasterone(CS)和芸苔(BL),但不是Dolichosterone(DS),在野生型表型中逆转。 DW1中内源性BRS的定量分析中发现了DS和降低Cs的积累。从DWF1制备的酶溶液不能将6-脱氧剂和DS和DS转化为CS,如野生型或35s:DWF1转基因植物所见。这表明DWF1不仅具有甾醇C-24还原酶的酶活性,而且还具有酶活性,但也具有拟拟合6-脱氧和DS的C-24将C-24减少6-脱氧和拟南芥的Cs。在BR缺陷型突变体(Det2 35s:DWF1)中的DWF1的过度表达明显拯救了Det2中发现的异常,表明DWF1在拟南芥中活性Brs的生物合成中的功能。 DWF1的表达通过施用Cs和Bl和Br-Modomant突变体BES1-D而下调。 DWF1推定启动子区域的E箱直接与BR转录因子BES1结合,暗示DWF1表达通过BES1通过BR信号进行反馈调节。总体而言,24-甲基BR的生物合成是用于产生Cs的替​​代途径,其被拟南芥中的DWF1介导和调节。

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