Ulmasov T, Liu Z B, Hagen G, Guilfoyle T J
Department of Biochemistry, University of Missouri, Columbia 65211, USA.
Plant Cell. 1995 Oct;7(10):1611-23. doi: 10.1105/tpc.7.10.1611.
The auxin-responsive soybean GH3 gene promoter is composed of multiple auxin response elements (AuxREs), and each AuxRE contributes incrementally to the strong auxin inducibility to the promoter. Two independent AuxREs of 25 bp (D1) and 32 bp (D4) contain the sequence TGTCTC. Results presented here show that the TGTCTC element in D1 and D4 is required but not sufficient for auxin inducibility in carrot protoplast transient expression assays. Additional nucleotides upstream of TGTCTC are also required for auxin inducibility. These upstream sequences showed constitutive activity and no auxin inducibility when part or all of the TGTCTC element was mutated or deleted. In D1, the constitutive element overlaps the 5' portion of TGTCTC; in D4, the constitutive element is separated from TGTCTC. An 11-bp element in D1, CCTCGTGTCTC, conferred auxin inducibility to a minimal cauliflower mosaic virus 35S promoter in transgenic tobacco seedlings as well as in carrot protoplasts (i.e., transient expression assays). Both constitutive elements bound specifically to plant nuclear proteins, and the constitutive element in D1 bound to a recombinant soybean basic leucine zipper transcription factor with G-box specificity. To demonstrate further the composite nature of AuxREs and the ability of the TGTCTC element to confer auxin inducibility, we created a novel AuxRE by placing a yeast GAL4 DNA binding site adjacent to the TGTCTC element. Expression of a GAL4-c-Rel transactivator in the presence of this novel AuxRE resulted in auxin-inducible expression. Our results indicate that at least some AuxREs have a composite structure consisting of a constitutive element adjacent to a conserved TGTCTC element that confers auxin inducibility.
生长素响应型大豆GH3基因启动子由多个生长素响应元件(AuxREs)组成,每个AuxRE对启动子的强生长素诱导性都有渐进贡献。两个分别为25 bp(D1)和32 bp(D4)的独立AuxREs含有序列TGTCTC。本文给出的结果表明,在胡萝卜原生质体瞬时表达试验中,D1和D4中的TGTCTC元件是生长素诱导性所必需的,但并不充分。TGTCTC上游的其他核苷酸对于生长素诱导性也是必需的。当TGTCTC元件的部分或全部发生突变或缺失时,这些上游序列表现出组成型活性且无生长素诱导性。在D1中,组成型元件与TGTCTC的5'部分重叠;在D4中,组成型元件与TGTCTC分离。D1中的一个11 bp元件CCTCGTGTCTC在转基因烟草幼苗以及胡萝卜原生质体中(即瞬时表达试验)赋予了最小花椰菜花叶病毒35S启动子生长素诱导性。两个组成型元件都能特异性结合植物核蛋白,D1中的组成型元件能结合具有G盒特异性的重组大豆碱性亮氨酸拉链转录因子。为了进一步证明AuxREs的复合性质以及TGTCTC元件赋予生长素诱导性的能力,我们通过将酵母GAL4 DNA结合位点置于TGTCTC元件附近创建了一个新的AuxRE。在存在这种新的AuxRE的情况下,GAL4-c-Rel反式激活因子的表达导致了生长素诱导性表达。我们的结果表明,至少一些AuxREs具有复合结构,由与赋予生长素诱导性的保守TGTCTC元件相邻的组成型元件组成。