Colombo L, Franken J, Koetje E, van Went J, Dons H J, Angenent G C, van Tunen A J
Department of Developmental Biology, DLO-Centre for Plant Breeding and Reproduction Research, Wageningen, The Netherlands.
Plant Cell. 1995 Nov;7(11):1859-68. doi: 10.1105/tpc.7.11.1859.
In contrast to the wealth of information relating to genes regulating floral meristem and floral organ identity, only limited data are available concerning genes that are involved in determining and regulating the identity and development of an ovule. We have recently isolated the floral binding protein 11 (FBP11) MADS box gene from petunia and found that it is expressed exclusively in ovule primordia and subsequently in the ovules, suggesting a role for this gene in ovule formation. To test this hypothesis, we constructed a recombinant gene in which the full-size FBP11 cDNA was placed under the control of a strong cauliflower mosaic virus 35S promoter. Transgenic petunia plants expressing this chimeric gene have ovulelike structures on the adaxial side of the sepals and the abaxial side of the petals. Detailed morphological studies showed that these ovulelike structures are true ovules. RNA gel blot analysis was performed to investigate ectopic FBP11 expression in relation to the expression of the closely related FBP7 gene and the putative petunia class C-type homeotic genes FBP6 and pMADS3. Our results indicate that FBP11 represents an ovule identity gene. A new model describing the mode of action of FBP11 as an additional class D MADS box gene is presented.
与调控花分生组织和花器官特征的基因所拥有的丰富信息形成对比的是,关于参与决定和调控胚珠特征与发育的基因,仅有有限的数据可用。我们最近从矮牵牛中分离出了花结合蛋白11(FBP11)MADS盒基因,并发现它仅在胚珠原基中表达,随后在胚珠中表达,这表明该基因在胚珠形成中发挥作用。为了验证这一假设,我们构建了一个重组基因,其中全长FBP11 cDNA置于强花椰菜花叶病毒35S启动子的控制之下。表达这个嵌合基因的转基因矮牵牛植株在萼片的近轴面和花瓣的远轴面有胚珠样结构。详细的形态学研究表明这些胚珠样结构是真正的胚珠。进行了RNA凝胶印迹分析,以研究异位FBP11表达与密切相关的FBP7基因以及推定的矮牵牛C类同源异型基因FBP6和pMADS3表达的关系。我们的结果表明FBP11代表一个胚珠特征基因。提出了一个描述FBP11作为额外的D类MADS盒基因作用模式的新模型。