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指导嵌合I类马铃薯块茎蛋白启动子/GUS基因融合体块茎特异性和蔗糖诱导型表达的顺式调控元件。

cis regulatory elements directing tuber-specific and sucrose-inducible expression of a chimeric class I patatin promoter/GUS-gene fusion.

作者信息

Liu X J, Prat S, Willmitzer L, Frommer W B

机构信息

Institut für Genbiologische Forschung Berlin GmbH, FRG.

出版信息

Mol Gen Genet. 1990 Sep;223(3):401-6. doi: 10.1007/BF00264446.

Abstract

The 5'-upstream region of the class I patatin gene B33 directs strong expression of the beta-glucuronidase (GUS) reporter gene in potato tubers and in leaves treated with sucrose. Cis-acting elements affecting specificity and level of expression were identified by deletion analysis in transgenic potato plants. A putative tuber-specific element is located downstream from position -195. Nuclear proteins present in leaf and tuber extracts bind specifically to a conserved AT rich motif within this region. A DNA fragment between -183 and -143, including the binding site is, however, not able to enhance the expression of a truncated 35S promoter from cauliflower mosaic virus. Independent positive elements contributing to a 100-fold increase relative to the basic tuber-specific element are located between -228 and -195; -736 and -509, -930 and -736 and -1512 and -951. Sucrose inducibility is controlled by sequences downstream of position -228, indicating that the tuber-specific and sucrose-inducible elements are in close proximity.

摘要

I类Patatin基因B33的5'上游区域可指导β-葡萄糖醛酸酶(GUS)报告基因在马铃薯块茎和经蔗糖处理的叶片中强烈表达。通过对转基因马铃薯植株进行缺失分析,确定了影响表达特异性和水平的顺式作用元件。一个假定的块茎特异性元件位于-195位下游。叶片和块茎提取物中存在的核蛋白与该区域内一个保守的富含AT的基序特异性结合。然而,-183至-143之间的一个包含结合位点的DNA片段并不能增强花椰菜花叶病毒截短的35S启动子的表达。相对于基本的块茎特异性元件,导致表达增加100倍的独立正向元件位于-228至-195之间;-736至-509之间、-930至-736之间以及-1512至-951之间。蔗糖诱导性受-228位下游序列控制,这表明块茎特异性元件和蔗糖诱导性元件紧密相邻。

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