Fiedler U, Filistein R, Wobus U, Bäumlein H
Institute of Plant Genetics and Crop Plant Research, Gatersleben, Germany.
Plant Mol Biol. 1993 Jul;22(4):669-79. doi: 10.1007/BF00047407.
We have identified cis-regulatory elements within the 5'-upstream region of a Vicia faba non-storage seed protein gene, called usp, by studying the expression of usp-promoter deletion fragments fused to reporter genes in transgenic tobacco seeds. 0.4 kb of usp upstream sequence contain at least six, but probably more, distinct cis-regulatory elements which are responsible for seemingly all quantitative, spatial and temporal aspects of expression. Expression-increasing and -decreasing elements are interspersed and include an AT-rich sequence, a G-box element and a CATGCATG motif. The latter acts as a negative element in contrast to what has been found for the same motif in legumin- and vicilin-type seed storage protein gene promoters. Seed specificity of expression is mainly determined by the -68/+51 region which confers, however, only very low levels of expression. The data support the combinatorial model of promoter function.
通过研究与报告基因融合的蚕豆非贮藏种子蛋白基因usp的5'-上游区域内顺式调控元件在转基因烟草种子中的表达,我们已鉴定出这些元件。usp上游序列的0.4 kb至少包含六个,但可能更多不同的顺式调控元件,这些元件似乎负责表达的所有定量、空间和时间方面。增加表达和降低表达的元件相互穿插,包括富含AT的序列、G-box元件和CATGCATG基序。与在豆球蛋白和豌豆球蛋白型种子贮藏蛋白基因启动子中发现的相同基序相反,后者作为负调控元件。表达的种子特异性主要由-68/+51区域决定,然而该区域仅赋予非常低水平的表达。这些数据支持启动子功能的组合模型。