Lee I, Wolfe D S, Nilsson O, Weigel D
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.
Curr Biol. 1997 Feb 1;7(2):95-104. doi: 10.1016/s0960-9822(06)00053-4.
. Development of petals and stamens in Arabidopsis flowers requires the function of the organ-identity gene APETALA3 (AP3), whose RNA is expressed specifically in petal and stamen primordia. AP3 expression is positively regulated by the meristem-identity gene LEAFY (LFY), which is expressed ubiquitously in young flowers. It is unknown how the transition from ubiquitous expression of LFY to region-specific expression of AP3 is made. It has previously been proposed for Antirrhinum that another gene, FIMBRIATA (FIM), mediates between the LFY and AP3 orthologs, with the three genes acting in a simple regulatory hierarchy. FIM is activated later than the LFY ortholog, and its expression is more restricted than that of the LFY ortholog.
. We have tested whether the model proposed for Antirrhinum applies to Arabidopsis, by creating transgenic plants in which the FIM ortholog UNUSUAL FLORAL ORGANS (UFO) was expressed constitutively from the promoter of the cauliflower mosaic virus 35S gene. In 35S::UFO flowers, AP3 was expressed precociously and ectopically, confirming that UFO is an upstream regulator of AP3. However, 35S::UFO could not restore petal and stamen development in lfy mutants, indicating that UFO can only function in the presence of LFY activity. The failure of 35S::UFO to rescue lfy mutants is consistent with our observation that UFO expression levels are not markedly changed in lfy mutants.
. We conclude that UFO is not a simple mediator between meristem- and organ-identity genes, but is likely to be a partially dispensable co-regulator that acts together with LFY. The interplay between LFY and UFO provides a paradigm for how a global regulator such as LFY activates selected target genes only in restricted regions within its expression domain.
拟南芥花中花瓣和雄蕊的发育需要器官特征基因APETALA3(AP3)的功能,其RNA在花瓣和雄蕊原基中特异性表达。AP3的表达受分生组织特征基因LEAFY(LFY)的正向调控,LFY在幼花中普遍表达。目前尚不清楚LFY从普遍表达向AP3区域特异性表达的转变是如何实现的。此前有人提出,对于金鱼草而言,另一个基因FIMBRIATA(FIM)在LFY和AP3的直系同源基因之间起介导作用,这三个基因以简单的调控层级发挥作用。FIM的激活晚于LFY的直系同源基因,其表达比LFY的直系同源基因更具局限性。
我们通过创建转基因植物来测试为金鱼草提出的模型是否适用于拟南芥,在这些转基因植物中,FIM的直系同源基因异常花器官(UFO)由花椰菜花叶病毒35S基因的启动子组成型表达。在35S::UFO花中,AP3过早且异位表达,证实UFO是AP3的上游调节因子。然而,35S::UFO无法恢复lfy突变体中花瓣和雄蕊的发育,表明UFO仅在LFY活性存在时才能发挥作用。35S::UFO无法拯救lfy突变体与我们观察到的lfy突变体中UFO表达水平没有明显变化一致。
我们得出结论,UFO不是分生组织和器官特征基因之间的简单介导因子,而可能是与LFY共同作用的部分可替代的共调节因子。LFY和UFO之间的相互作用为诸如LFY这样的全局调节因子如何仅在其表达域内的受限区域激活选定的靶基因提供了一个范例。