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

机译:DWARF1作为C-24还原酶在拟南芥油菜素类固醇生物合成中的功能和分子调控

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摘要

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(DWF1)是固醇C-24还原酶,可催化拟南芥中24-亚甲基胆固醇(24-MCHR)转化为菜油甾醇(CR)。功能丧失的突变体dwf1显示出与油菜素固醇(BR)缺陷型突变体相似的表型异常。这些异常在野生型表型中是通过外源应用Castasterone(CS)和Brasinolide(BL)而不是dolichosterone(DS)来逆转的。在dwf1中内源性BR的定量分析中发现了DS的积累和CS的降低。如在野生型或35S:DWF1转基因植物中所见,由dwf1制备的酶溶液无法将6-deoxoDS转化为6-deoxoCS,将DS转化为CS。这表明DWF1不仅对固醇C-24还原酶具有酶活性,而且对于在拟南芥属中催化C-24将6-deoxoDS还原为6-deoxoCS和将DS还原为CS的BR C-24还原酶具有酶活性。 BR缺陷突变体(det2 35S:DWF1)中DWF1的过表达清楚地拯救了det2中发现的异常,表明DWF1在拟南芥中活性BR的生物合成中起作用。通过应用CS和BL以及BR显性突变体bes1-D,DWF1的表达下调。 DWF1的推定启动子区域中的E-box直接与BR转录因子BES1结合,这意味着DWF1的表达受BES1的BR信号反馈调节。总的来说,生物合成24-亚甲基BR是产生CS的另一种途径,它是由拟南芥中的DWF1介导和调控的。

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