Stanford A C, Northcote D H, Bevan M W
Molecular Genetics Department, IPSR Cambridge Laboratory, UK.
EMBO J. 1990 Mar;9(3):593-603. doi: 10.1002/j.1460-2075.1990.tb08151.x.
Transcriptional fusions between the gene encoding win2 from potato and the reporter gene encoding beta-glucuronidase (GUS) have been used to study the spatial and temporal patterns of wound induced gene activity in transgenic potato and tobacco plants. Gene fusions containing a full length win2 promoter were found to be correctly regulated in response to mechanical wounding in transgenic potato, but not in the heterologous host, tobacco. Sequences greater than 560 bp upstream of the transcription start site of win2 were shown to be important for wound inducibility. The dramatic induction of GUS activity detected using fluorometric assays of extracts of wounded and aged leaves of several independent win2--GUS transformants was consistent with the kinetics of win2 mRNA accumulation. Histochemical analysis of wounded leaves showed that transcription first occurred in cells immediately adjacent to the wound, and was then progressively induced in cells associated with the vascular system at a distance from the wound site. In tubers, a localized response to wounding was observed, and this only spread to other parts of the tuber if it had started to sprout. It was concluded that active vascular transport was necessary for the spread of wound response. Win2--GUS fusions were also expressed as part of normal plant development, as GUS activity was detected in the developing buds and in a layer of cells associated with the lenticels of unwounded tubers.
编码马铃薯win2的基因与编码β-葡萄糖醛酸酶(GUS)的报告基因之间的转录融合已被用于研究转基因马铃薯和烟草植株中伤口诱导基因活性的时空模式。发现含有全长win2启动子的基因融合在转基因马铃薯中对机械损伤有正确的调控反应,但在异源宿主烟草中则不然。已证明win2转录起始位点上游大于560 bp的序列对伤口诱导性很重要。使用荧光分析法对几个独立的win2-GUS转化体的受伤和衰老叶片提取物进行检测,发现GUS活性的显著诱导与win2 mRNA积累的动力学一致。对受伤叶片的组织化学分析表明,转录首先发生在紧邻伤口的细胞中,然后在远离伤口部位的与维管系统相关的细胞中逐渐诱导。在块茎中,观察到对伤口的局部反应,并且只有在块茎开始发芽时,这种反应才会扩散到块茎的其他部位。得出的结论是,活跃的维管运输对于伤口反应的扩散是必要的。Win2-GUS融合也作为正常植物发育的一部分表达,因为在发育中的芽和未受伤块茎皮孔相关的一层细胞中检测到了GUS活性。