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玉米醇脱氢酶1(Adh1)基因厌氧反应元件的功能特性

Functional properties of the anaerobic responsive element of the maize Adh1 gene.

作者信息

Olive M R, Walker J C, Singh K, Dennis E S, Peacock W J

机构信息

CSIRO Division of Plant Industry, Canberra, A.C.T., Australia.

出版信息

Plant Mol Biol. 1990 Oct;15(4):593-604. doi: 10.1007/BF00017834.

Abstract

The functional properties of the anaerobic responsive element (ARE) of the maize Adh1 gene have been analysed using a transient expression assay in electroporated maize protoplasts. The ARE functions in both orientations although inversion of the ARE sequence relative to the TATA box element produces slightly weaker promoter activity under anaerobic conditions and elevated expression under aerobic conditions. Promoter activity under anaerobic conditions is proportional to the number of complete ARE sequences in the Adh1 promoter. The ARE contains two sub-regions and dimers of sub-region II are as efficient as the wild-type sequence in activating gene expression under anaerobic conditions. However, sub-region I dimers do not appear capable of inducing gene expression in response to anaerobic stress. We conclude that sub-region II is essential for anaerobic induction of gene expression. Reporter gene expression remains constant when the spacing between sub-regions of the ARE is increased up to at least 64 bp, but increased spacing of 136 bp or greater abolishes expression in both aerobic and anaerobic conditions, indicating that a close association of the two sub-regions is required both for anaerobic responsiveness and for maximal levels of aerobic gene expression. When the ARE is placed upstream of position -90 of the CaMV 35S promoter, the ARE produces a high level of expression in both aerobic and anaerobic conditions. The general enhancement of gene expression driven by the hybrid ARE/35S promoter in aerobic conditions requires an intact sub-region II motif since mutation or deletion of sub-region II from the hybrid promoter reduces the level of expression to that observed for the truncated 35S promoter alone. In addition, mutation of the sub-region I sequences in the ARE/35S hybrid promoter does not significantly reduce expression in aerobic conditions, relative to pARE/delta 35S(-90), suggesting that sub-region I does not contribute to this general enhancer function.

摘要

利用电穿孔玉米原生质体中的瞬时表达分析,对玉米乙醇脱氢酶1(Adh1)基因的厌氧反应元件(ARE)的功能特性进行了分析。ARE在两个方向上均起作用,尽管相对于TATA盒元件,ARE序列的倒置在厌氧条件下产生的启动子活性略弱,而在需氧条件下表达升高。厌氧条件下的启动子活性与Adh1启动子中完整ARE序列的数量成正比。ARE包含两个亚区域,在厌氧条件下,亚区域II的二聚体在激活基因表达方面与野生型序列一样有效。然而,亚区域I的二聚体似乎不能响应厌氧胁迫诱导基因表达。我们得出结论,亚区域II对于基因表达的厌氧诱导至关重要。当ARE亚区域之间的间距增加到至少64 bp时,报告基因的表达保持不变,但增加到136 bp或更大的间距会消除需氧和厌氧条件下的表达,这表明两个亚区域的紧密关联对于厌氧反应性和需氧基因表达的最大水平都是必需的。当ARE置于花椰菜花叶病毒(CaMV)35S启动子-90位置的上游时,ARE在需氧和厌氧条件下均产生高水平的表达。在需氧条件下,由ARE/35S杂交启动子驱动的基因表达的总体增强需要完整的亚区域II基序,因为从杂交启动子中突变或缺失亚区域II会将表达水平降低到单独的截短35S启动子所观察到的水平。此外,相对于pARE/δ35S(-90),ARE/35S杂交启动子中亚区域I序列的突变在需氧条件下不会显著降低表达,这表明亚区域I对这种一般增强子功能没有贡献。

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