Rouster J, Leah R, Mundy J, Cameron-Mills V
Carlsberg Research Laboratory, Copenhagen, Denmark.
Plant J. 1997 Mar;11(3):513-23. doi: 10.1046/j.1365-313x.1997.11030513.x.
A genomic DNA fragment was isolated containing 5' upstream sequences and part of the open reading frame corresponding to the lipoxygenase 1 cDNA (LoxA) expressed in barley grains during development and germination. Lox1 transcription was shown to be methyl jasmonate (MeJA)- and wound-inducible in leaves, but Lox1 transcripts were not detected in mildew-infected leaves, although this is a commonly observed response to pathogenic attack in various plants. Transient gene expression assays were used to identify a promoter region involved in MeJA-responsive expression. Analysis of 5' and 3' promoter deletions indicated that sequences between -363 and -294 conferred MeJA-responsive expression. Deletions/replacements covering this part of the promoter further defined a MeJA-responsive region between -331 and -291. Insertion of the region -328 to -293 into the constitutive CaMV 35S promoter conferred MeJA-responsive expression. The 36 bp fragment contains the motif TGACG as inverted repeats, which has been previously identified as a binding site for bZIP transactivating factors. Site-directed mutagenesis on these TGACG motifs abolished MeJA-responsive expression, clearly identifying them as MeJA-responsive elements. Sequence comparisons found no similar motif in other characterized promoters of MeJA-inducible genes, but suggested a common spatial structure which may serve as a binding site for transacting factors involved in the MeJA signal transduction pathway.
分离出一个基因组DNA片段,其包含5'上游序列以及对应于大麦籽粒在发育和萌发过程中表达的脂氧合酶1 cDNA(LoxA)的部分开放阅读框。Lox1转录在叶片中显示受茉莉酸甲酯(MeJA)和伤口诱导,但在白粉病感染的叶片中未检测到Lox1转录本,尽管这是各种植物中对病原体攻击常见的反应。使用瞬时基因表达分析来鉴定参与MeJA响应表达的启动子区域。对5'和3'启动子缺失的分析表明,-363至-294之间的序列赋予MeJA响应表达。覆盖启动子这一部分的缺失/替换进一步确定了-331至-291之间的MeJA响应区域。将-328至-293区域插入组成型CaMV 35S启动子中赋予了MeJA响应表达。36 bp片段包含作为反向重复的TGACG基序,其先前已被鉴定为bZIP反式激活因子的结合位点。对这些TGACG基序进行定点诱变消除了MeJA响应表达,明确将它们鉴定为MeJA响应元件。序列比较在MeJA诱导基因的其他特征启动子中未发现类似基序,但暗示了一种可能作为参与MeJA信号转导途径的反式作用因子结合位点的共同空间结构。