van der Meer I M, Stam M E, van Tunen A J, Mol J N, Stuitje A R
Department of Genetics, Vrije Universiteit, Amsterdam, The Netherlands.
Plant Cell. 1992 Mar;4(3):253-62. doi: 10.1105/tpc.4.3.253.
Inhibition of flower pigmentation in transgenic petunia plants was previously accomplished by expressing an antisense chalcone synthase (chs) gene under the control of the cauliflower mosaic virus (CaMV) 35S promoter. This chimeric gene was not effective in inhibiting pigmentation in anthers, presumably because the viral CaMV 35S promoter was insufficiently expressed in cell types of this organ in which the pigments are produced. Insertion of the anther box, a homologous sequence found in other genes expressed in anthers, resulted in a modified expression pattern driven by this promoter, as monitored by the beta-glucuronidase (gus) gene. In addition to the basic CaMV 35S expression pattern in anthers, GUS activity was observed in tapetum cells when the modified promoter was fused to the gus gene. This promoter construct was subsequently used to drive an antisense chs gene in transgenic petunia, which led to the inhibition of pigment synthesis in anthers of five of 35 transformants. Transgenic plants with white anthers were male sterile due to an arrest in male gametophyte development. This finding indicated that flavonoids play an essential role in male gametophyte development.
此前,通过在花椰菜花叶病毒(CaMV)35S启动子的控制下表达反义查尔酮合酶(chs)基因,实现了对转基因矮牵牛植株花色沉着的抑制。这种嵌合基因在抑制花药色素沉着方面并不有效,推测是因为病毒CaMV 35S启动子在该器官产生色素的细胞类型中表达不足。插入花药盒(在花药中表达的其他基因中发现的同源序列),导致了由该启动子驱动的修饰表达模式,这通过β-葡萄糖醛酸酶(gus)基因进行监测。当修饰后的启动子与gus基因融合时,除了在花药中具有基本的CaMV 35S表达模式外,在绒毡层细胞中也观察到了GUS活性。该启动子构建体随后被用于驱动转基因矮牵牛中的反义chs基因,这导致35个转化体中有5个的花药色素合成受到抑制。花药为白色的转基因植株由于雄配子体发育停滞而雄性不育。这一发现表明类黄酮在雄配子体发育中起着至关重要的作用。