Ulmasov T, Murfett J, Hagen G, Guilfoyle T J
Department of Biochemistry, University of Missouri, Columbia 65211, USA.
Plant Cell. 1997 Nov;9(11):1963-71. doi: 10.1105/tpc.9.11.1963.
A highly active synthetic auxin response element (AuxRE), referred to as DR5, was created by performing site-directed mutations in a natural composite AuxRE found in the soybean GH3 promoter. DR5 consisted of tandem direct repeats of 11 bp that included the auxin-responsive TGTCTC element. The DR5 AuxRE showed greater auxin responsiveness than a natural composite AuxRE and the GH3 promoter when assayed by transient expression in carrot protoplasts or in stably transformed Arabidopsis seedlings, and it provides a useful reporter gene for studying auxin-responsive transcription in wild-type plants and mutants. An auxin response transcription factor, ARF1, bound with specificity to the DR5 AuxRE in vitro and interacted with Aux/IAA proteins in a yeast two-hybrid system. Cotransfection experiments with natural and synthetic AuxRE reporter genes and effector genes encoding Aux/IAA proteins showed that overexpression of Aux/IAA proteins in carrot protoplasts resulted in specific repression of TGTCTC AuxRE reporter gene expression.
一种高度活跃的合成生长素响应元件(AuxRE),称为DR5,是通过对大豆GH3启动子中发现的天然复合AuxRE进行定点突变而创建的。DR5由11个碱基对的串联直接重复序列组成,其中包括生长素响应元件TGTCTC。当通过在胡萝卜原生质体中瞬时表达或在稳定转化的拟南芥幼苗中进行检测时,DR5 AuxRE比天然复合AuxRE和GH3启动子表现出更高的生长素响应性,并且它为研究野生型植物和突变体中的生长素响应转录提供了一个有用的报告基因。一种生长素响应转录因子ARF1在体外与DR5 AuxRE特异性结合,并在酵母双杂交系统中与Aux/IAA蛋白相互作用。用天然和合成AuxRE报告基因以及编码Aux/IAA蛋白的效应基因进行共转染实验表明,在胡萝卜原生质体中过表达Aux/IAA蛋白会导致TGTCTC AuxRE报告基因表达的特异性抑制。