Pouteau S, Nicholls D, Tooke F, Coen E, Battey N
Plant Science Laboratories, The University of Reading, Whiteknights, UK.
Development. 1997 Sep;124(17):3343-51. doi: 10.1242/dev.124.17.3343.
The mechanisms that establish the floral meristem are now becoming clearer, but the way in which flowering is maintained is less well understood. Impatiens balsamina provides a unique opportunity to address this question because reversion to vegetative growth can be obtained in a predictable way by transferring plants from inductive to non-inductive conditions. Following increasing amounts of induction, reversion takes place at progressively later stages of flower development. Partial flower induction and defoliation experiments show that a floral signal is produced in the cotyledon in response to inductive conditions and that this signal progressively diminishes after transfer to non-inductive conditions, during reversion. Therefore reversion in Impatiens is most likely due to the failure of leaves to become permanent sources of inductive signal in addition to the lack of meristem commitment to flowering. Analysis of the expression of the Impatiens homologues of the meristem identity genes floricaula and squamosa indicates that a change in floricaula transcription is not associated with the establishment or maintenance of the floral meristem in this species. Squamosa transcription is associated with floral development and petal initiation, and is maintained in existing petal or petaloid primordia even after the meristem has reverted. However, it is not expressed in the reverted meristem, in which leaves are initiated in whorled phyllotaxis and without axillary meristems, both characteristics usually associated with the floral meristem. These observations show that squamosa expression is not needed for the maintenance of these floral characters. The requirement for the production of the floral signal in the leaf during the process of flower development may reflect an additional function separate to that of squamosa activation; alternatively the signal may be required to ensure continued transcriptional activation in the meristem.
建立花分生组织的机制现在越来越清晰,但开花维持的方式却了解得较少。凤仙花提供了一个独特的机会来解决这个问题,因为通过将植物从诱导条件转移到非诱导条件,可以以可预测的方式实现向营养生长的逆转。随着诱导量的增加,逆转发生在花发育的逐渐后期阶段。部分花诱导和去叶实验表明,子叶在诱导条件下会产生一种花信号,并且在转移到非诱导条件下逆转过程中,该信号会逐渐减弱。因此,凤仙花的逆转很可能是由于除了分生组织对开花缺乏决定性之外,叶片未能成为诱导信号的持续来源。对分生组织特征基因floricaula和squamosa的凤仙花同源物表达的分析表明,floricaula转录的变化与该物种花分生组织的建立或维持无关。Squamosa转录与花发育和花瓣起始相关,即使在分生组织逆转后,也会在现有的花瓣或花瓣状原基中维持。然而,它在逆转的分生组织中不表达,在该分生组织中,叶片以轮状叶序起始且没有腋生分生组织,这两个特征通常与花分生组织相关。这些观察结果表明,维持这些花特征不需要squamosa表达。在花发育过程中叶片产生花信号的需求可能反映了一种与squamosa激活功能不同的额外功能;或者该信号可能是确保分生组织中持续转录激活所必需的。