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首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Promoter analysis of the Catharanthus roseus geraniol 10-hydroxylase gene involved in terpenoid indole alkaloid biosynthesis
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Promoter analysis of the Catharanthus roseus geraniol 10-hydroxylase gene involved in terpenoid indole alkaloid biosynthesis

机译:长春花香叶香叶醇10-羟化酶基因的启动子分析与萜类吲哚生物碱的合成有关

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Geraniol 10-hydroxylase (G10H) is an important enzyme in the biosynthetic pathway of monoterpenoid alkaloids found in diverse plant species. The Catharanthus roseus G10H controls the first committed step in biosynthesis of terpenoid indole alkaloids (TIA). The C roseus G10H promoter sequence was isolated by a PCR-based genome walking method. Sequence analysis revealed that the G10H promoter contains several potential eukaryotic regulatory elements involved in regulation of gene expression. The major transcription start site of the promoter was mapped to an adenine 31 bp downstream of the TATA-box. For functional characterization, transcriptional fusions between the G10H promoter fragments with 5' or 3' deletions and the GUS reporter gene were generated and their expressions were analyzed in a tobacco protoplast transient expression assay. Deletion of the promoter down to -318 bp had little effect on GUS activity. However, further deletion of the promoter to position -103 resulted in approximately 5-fold reduction of GUS activity. Gain-of-function experiments revealed the presence of three potential transcriptional enhancers located in regions between -191 and -147, -266 and -188, and -318 and -266, respectively. The G10H promoter was capable of conferring stable GUS expression in transgenic tobacco plants and C. roseus hairy roots. In transgenic tobacco seedlings GUS expression was tissue-specific, restricted to leaf and actively growing cells around the root tip, and not detected in the hypocotyls, root cap and older developing areas of the root. The GUS expression in both transgenic C. roseus hairy roots and tobacco seedlings were responsive to fungal elicitor and methyljasmonate. Compared to other known promoters of TIA pathway genes, the G10H promoter contains unique binding sites for several transcription factors, suggesting that the G10H promoter may be regulated by a different transcriptional cascade. (c) 2007 Elsevier B.V. All rights reserved.
机译:香叶醇10-羟化酶(G10H)是在多种植物物种中发现的单萜生物碱生物合成途径中的重要酶。长春花G10H控制着萜类吲哚生物碱(TIA)生物合成中的第一步。通过基于PCR的基因组步移方法分离了玫瑰蔷薇G10H启动子序列。序列分析显示,G10H启动子含有几种潜在的真核调控元件,参与基因表达的调控。启动子的主要转录起始位点位于TATA-box下游31 bp的腺嘌呤上。为了进行功能表征,产生了具有5'或3'缺失的G10H启动子片段与GUS报道基因之间的转录融合,并在烟草原生质体瞬时表达测定中分析了它们的表达。启动子缺失至-318 bp对GUS活性影响很小。然而,将启动子进一步缺失至-103位导致GUS活性降低约5倍。功能获得实验显示存在三种潜在的转录增强子,分别位于-191和-147,-266和-188和-318和-266之间。 G10H启动子能够在转基因烟草植物和玫瑰假丝酵母毛状根中提供稳定的GUS表达。在转基因烟草幼苗中,GUS表达是组织特异性的,仅限于叶和根尖周围活跃生长的细胞,而在下胚轴,根冠和较老的根部未发现。在转基因玫瑰假丝酵母毛状根和烟草幼苗中,GUS表达均对真菌激发剂和茉莉酸甲酯有反应。与TIA途径基因的其他已知启动子相比,G10H启动子包含几个转录因子的独特结合位点,表明G10H启动子可能受不同的转录级联调控。 (c)2007 Elsevier B.V.保留所有权利。

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