Maghuly Fatemeh, Khan Mahmood Ali, Fernandez Eduviges Borroto, Druart Philippe, Watillon Bernard, Laimer Margit
Plant Biotechnology Unit, Biotechnology Department, BOKU University, Muthgasse 18, 1190 Vienna, Austria.
J Biotechnol. 2008 May 20;135(1):105-16. doi: 10.1016/j.jbiotec.2008.02.021. Epub 2008 Mar 4.
The fact that calmodulin genes (CaM) are tightly associated with the Ca(2+) regulatory pathway, as well as their putative role in plant defence against pathogens, indicate a potential use of alternative plant promoters to express genes of interest in specific tissues or developmental stages. To study the expression level of the apple CaM promoter, 981 bp sequences upstream were fused to the uidA gene, introduced into cherry and compared with a 35S-GUS construct. Transgene copy number and transgenic expression levels were analysed using Southern blot, Western blot and RT-PCR techniques. Transcription levels were assessed by GUS fluorometry, histochemistry and real-time PCR techniques in leaves of plantlets grown in vitro under various abiotic stresses like low- and high-temperature, salicylic acid and wounding, harvested after 0, 0.5, 1, 2, 4, 10, 24 and 72 h. Histochemical analyses showed staining only in veins and petioles of CaM-GUS lines, while in 35S-GUS plants staining extended to the entire leaf. Furthermore, real-time qPCR data indicate that both promoters are differently regulated by various stresses. Obtained results suggest that the selected apple CaM promoter responsible for the expression of a gene in vascular tissues may offer interesting perspectives for plant defense programs.
钙调蛋白基因(CaM)与Ca(2+)调节途径紧密相关,以及它们在植物抵御病原体中的假定作用,这表明利用替代植物启动子在特定组织或发育阶段表达感兴趣基因具有潜在用途。为了研究苹果CaM启动子的表达水平,将上游981 bp序列与uidA基因融合,导入樱桃,并与35S-GUS构建体进行比较。使用Southern印迹、Western印迹和RT-PCR技术分析转基因拷贝数和转基因表达水平。通过GUS荧光测定法、组织化学和实时PCR技术,在不同非生物胁迫(如低温和高温、水杨酸和创伤)下体外培养的幼苗叶片中,于0、0.5、1、2、4、10、24和72小时后收获,评估转录水平。组织化学分析显示,CaM-GUS系仅在叶脉和叶柄中染色,而在35S-GUS植物中,染色扩展至整片叶子。此外,实时定量PCR数据表明,两种启动子受不同胁迫的调控方式不同。所得结果表明,负责在维管组织中表达基因的所选苹果CaM启动子可能为植物防御计划提供有趣的前景。