Walz Alexander, Seidel Claudia, Rusak Gordana, Park Seijin, Cohen Jerry D, Ludwig-Müller Jutta
Institut für Botanik, Technische Universität Dresden, Dresden, Germany.
Planta. 2008 Apr;227(5):1047-61. doi: 10.1007/s00425-007-0679-8. Epub 2007 Dec 21.
The seed protein IAP1 from bean (PvIAP1; Phaseolus vulgaris L.) that is modified by the phytohormone indole-3-acetic acid (IAA) was heterologously expressed in the two reference plant species Arabidopsis thaliana and Medicago truncatula. For the transformation of Medicago we devised a novel protocol using seedling infiltration. When PvIAP1 was overexpressed under the control of the constitutive 35SCaMV promoter in Arabidopsis, the plants showed signs of earlier bolting and enhanced branching. Expression of a fusion protein of PvIAP1 with both a green fluorescence protein (GFP) as reporter and 6x histidine (His) tag under the control of the native bean IAP1 promoter resulted in the accumulation of the protein in both plant species exclusively in seeds as shown by immunoblotting and by fluorescence microscopy. During seed development, PvIAP1 was first expressed in the vascular bundle of Arabidopsis, whereas in later stages GFP fluorescence was visible essentially in all tissues of the seed. Fluorescence decreased rapidly after imbibition in the seeds for both Arabidopsis and Medicago, although the fluorescence persisted longer in Arabidopsis. GFP fluorescence was distributed evenly between an organelle fraction, the microsomal membrane fraction, and the cytosol. This was also confirmed by immunoblot analysis. Clusters of higher GFP fluorescence were observed by confocal microscopy. Although PvIAP1 protein accumulated in seeds of both Arabidopsis and Medicago, neither species post-translationally modified the protein with an indoleacyl moiety as shown by quantitative GC-MS analysis after alkaline hydrolysis. These results indicate an apparent specificity for IAA attachment in different plant species.
来自菜豆(PvIAP1;菜豆属普通菜豆)的种子蛋白IAP1被植物激素吲哚-3-乙酸(IAA)修饰后,在两种模式植物拟南芥和蒺藜苜蓿中进行了异源表达。对于蒺藜苜蓿的转化,我们设计了一种使用幼苗浸润的新方案。当PvIAP1在组成型35SCaMV启动子的控制下在拟南芥中过表达时,植株表现出提前抽薹和分枝增强的迹象。在菜豆IAP1天然启动子的控制下,PvIAP1与绿色荧光蛋白(GFP)作为报告基因和6x组氨酸(His)标签的融合蛋白的表达导致该蛋白在两种植物中仅在种子中积累,这通过免疫印迹和荧光显微镜观察得以证实。在种子发育过程中,PvIAP1首先在拟南芥的维管束中表达,而在后期阶段,GFP荧光基本上在种子的所有组织中都可见。拟南芥和蒺藜苜蓿种子吸胀后荧光迅速下降,尽管拟南芥中的荧光持续时间更长。GFP荧光均匀分布在细胞器部分、微粒体膜部分和细胞质中。免疫印迹分析也证实了这一点。通过共聚焦显微镜观察到较高GFP荧光的聚集。尽管PvIAP1蛋白在拟南芥和蒺藜苜蓿的种子中积累,但如碱性水解后的定量气相色谱-质谱分析所示,两种植物都没有对该蛋白进行吲哚酰基部分的翻译后修饰。这些结果表明不同植物物种中IAA附着具有明显的特异性。