Rech Philippe, Grima-Pettenati Jacqueline, Jauneau Alain
IFR40, UMR CNRS-UPS 5546, Signaux et Messages Cellulaires chez les Végétaux, Pôle de Biotechnologie Végétale, BP 17, Auzeville, 31326 Castanet Tolosan, France.
Plant J. 2003 Jan;33(1):205-9. doi: 10.1046/j.1365-313x.2003.016017.x.
We have previously shown that the Eucalyptus gunnii EgCAD2 promoter was preferentially expressed in vascular tissues in different transgenic plants (poplar, tobacco, Arabidopsis and grapevine). In order to delineate the cis elements governing this vascular expression pattern, promoter deletion analysis was performed allowing us to identify the proximal region [-340/-124] as essential for vascular cambium/xylem-specific expression. In plants transformed with the smallest promoter region [-124/+117], the GUS activity was difficult to detect using conventional bright field microscopy. To overcome this problem, we used fluorescence microscopy, enabling us to show that the [-124/+117] region contained cis-elements driving activity in phloem fibres but not in secondary xylem. The technical improvement of the histochemical detection of GUS activity using fluorescence microscopy enables accurate investigation of low GUS activity in phenol-rich tissues.
我们之前已经表明,冈尼桉EgCAD2启动子在不同的转基因植物(杨树、烟草、拟南芥和葡萄)的维管组织中优先表达。为了确定控制这种维管表达模式的顺式元件,我们进行了启动子缺失分析,从而使我们能够确定近端区域[-340/-124]对于维管形成层/木质部特异性表达至关重要。在用最小启动子区域[-124/+117]转化的植物中,使用传统的明场显微镜很难检测到GUS活性。为了克服这个问题,我们使用了荧光显微镜,这使我们能够表明[-124/+117]区域包含在韧皮部纤维中驱动活性但不在次生木质部中驱动活性的顺式元件。使用荧光显微镜对GUS活性进行组织化学检测的技术改进能够准确研究富含酚类组织中的低GUS活性。