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拟南芥EF-1α基因启动子的模块化组织与发育活性

Modular organization and development activity of an Arabidopsis thaliana EF-1 alpha gene promoter.

作者信息

Curie C, Axelos M, Bardet C, Atanassova R, Chaubet N, Lescure B

机构信息

Laboratoire de Biologie Moléculaire des Relations Plantes-Microorganismes, CNRS-INRA, Castanet-Tolosan, France.

出版信息

Mol Gen Genet. 1993 Apr;238(3):428-36. doi: 10.1007/BF00292002.

Abstract

The activity of the Arabidopsis thalana A1 EF-1 alpha gene promoter was analyzed in transgenic Arabidopsis plants. The 5' upstream sequence of the A1 gene and several promoter deletions were fused to the beta-glucuronidase (GUS) coding region. Promoter activity was monitored by quantitative and histochemical assays of GUS activity. The results show that the A1 promoter exhibits a modular organization. Sequences both upstream and downstream relative to the transcription initiation site are involved in quantitative and tissue-specific expression during vegetative growth. One upstream element may be involved in the activation of expression in meristematic tissues; the downstream region, corresponding to an intron within the 5' non-coding region (5'IVS), is important for expression in roots; both upstream and downstream sequences are required for expression in leaves, suggesting combinatorial properties of EF-1 alpha cis-regulatory elements. This notion of specific combinatorial regulation is reinforced by the results of transient expression experiments in transfected Arabidopsis protoplasts. The deletion of the 5'IVS has much more effect on expression when the promoter activity is under the control of A1 EF-1 alpha upstream sequences than when these upstream sequences were replaced by the 35S enhancer. Similarly, a synthetic oligonucleotide corresponding to an A1 EF-1 alpha upstream cis-acting element (the TEF1 box), is able to restore partially the original activity when fused to a TEF1-less EF1-alpha promoter but has no significant effect when fused to an enhancer-less 35S promoter.

摘要

在转基因拟南芥植物中分析了拟南芥A1 EF-1α基因启动子的活性。将A1基因的5'上游序列和几个启动子缺失片段与β-葡萄糖醛酸酶(GUS)编码区融合。通过对GUS活性的定量和组织化学分析来监测启动子活性。结果表明,A1启动子呈现出模块化组织。相对于转录起始位点,上游和下游序列均参与营养生长期间的定量和组织特异性表达。一个上游元件可能参与分生组织中表达的激活;对应于5'非编码区(5'IVS)内一个内含子的下游区域,对根中的表达很重要;叶片中的表达需要上游和下游序列,这表明EF-1α顺式调控元件具有组合特性。转染的拟南芥原生质体中的瞬时表达实验结果强化了这种特定组合调控的概念。当启动子活性受A1 EF-1α上游序列控制时,5'IVS的缺失对表达的影响比这些上游序列被35S增强子取代时更大。同样,与A1 EF-1α上游顺式作用元件(TEF1框)对应的合成寡核苷酸,与无TEF1的EF1-α启动子融合时能够部分恢复原始活性,但与无增强子的35S启动子融合时没有显著影响。

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