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Cloning and Functional Analysis of the Promoter of an Ascorbate Oxidase Gene from Gossypium hirsutum

机译:陆地棉抗坏血酸氧化酶基因启动子的克隆与功能分析

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摘要

Apoplastic ascorbate oxidase (AO) plays significant roles in plant cell growth. However, the mechanism of underlying the transcriptional regulation of AO in Gossypium hirsutum remains unclear. Here, we obtained a 1,920-bp promoter sequence from the Gossypium hirsutum ascorbate oxidase (GhAO1) gene, and this GhAO1 promoter included a number of known cis-elements. Promoter activity analysis in overexpressing pGhAO1::GFP-GUS tobacco (Nicotiana benthamiana) showed that the GhAO1 promoter exhibited high activity, driving strong reporter gene expression in tobacco trichomes, leaves and roots. Promoter 5’-deletion analysis demonstrated that truncated GhAO1 promoters with serial 5’-end deletions had different GUS activities. A 360-bp fragment was sufficient to activate GUS expression. The P-1040 region had less GUS activity than the P-720 region, suggesting that the 320-bp region from nucleotide -720 to -1040 might include a cis-element acting as a silencer. Interestingly, an auxin-responsive cis-acting element (TGA-element) was uncovered in the promoter. To analyze the function of the TGA-element, tobacco leaves transformed with promoters with different 5’ truncations were treated with indole-3-acetic acid (IAA). Tobacco leaves transformed with the promoter regions containing the TGA-element showed significantly increased GUS activity after IAA treatment, implying that the fragment spanning nucleotides -1760 to -1600 (which includes the TGA-element) might be a key component for IAA responsiveness. Analyses of the AO promoter region and AO expression pattern in Gossypium arboreum (Ga, diploid cotton with an AA genome), Gossypium raimondii (Gr, diploid cotton with a DD genome) and Gossypium hirsutum (Gh, tetraploid cotton with an AADD genome) indicated that AO promoter activation and AO transcription were detected together only in D genome/sub-genome (Gr and Gh) cotton. Taken together, these results suggest that the 1,920-bp GhAO1 promoter is a functional sequence with a potential effect on fiber cell development, mediated by TGA-element containing sequences, via the auxin-signaling pathway.
机译:质外抗坏血酸氧化酶(AO)在植物细胞生长中起重要作用。然而,在陆地棉中AO转录调控的基础机制仍不清楚。在这里,我们从陆地棉抗坏血酸氧化酶(GhAO1)基因中获得了1,920-bp的启动子序列,该GhAO1启动子包括许多已知的顺式元件。过表达pGhAO1 :: GFP-GUS烟草(Nicotiana benthamiana)的启动子活性分析表明,GhAO1启动子表现出很高的活性,在烟草毛状体,叶片和根中驱动着很强的报告基因表达。启动子5’缺失分析表明具有5’末端序列缺失的截短的GhAO1启动子具有不同的GUS活性。一个360 bp的片段足以激活GUS表达。 P-1040区域的GUS活性低于P-720区域,这表明从核苷酸-720到-1040的320 bp区域可能包含顺式元件,作为沉默子。有趣的是,在启动子中发现了一种生长素反应性顺式作用元件(TGA元件)。为了分析TGA元素的功能,用吲哚-3-乙酸(IAA)处理了具有5'截短的启动子转化的烟叶。用含TGA元素的启动子区域转化的烟叶在IAA处理后显示出显着增加的GUS活性,这意味着跨核苷酸-1760至-1600的片段(包括TGA元素)可能是IAA响应能力的关键组成部分。指出了在棉(Ga,具有AA基因组的二倍体棉),雷氏棉(Gr,具有DD基因组的二倍体棉)和陆地棉(Gh,具有AADD基因组的四倍体棉)中的AO启动子区域和AO表达模式的分析。仅在D基因组/亚基因组(Gr和Gh)棉花中同时检测到 AO 启动子激活和 AO 转录。综上所述,这些结果表明1,920-bp GhAO1 启动子是一个功能序列,通过生长素信号途径,由含有TGA元素的序列介导,对纤维细胞的发育具有潜在的影响。

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  • 年(卷),期 -1(11),9
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  • 页码 e0161695
  • 总页数 13
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