Engelhorn Julia, Moreau Fanny, Fletcher Jennifer C, Carles Cristel C
Université Grenoble Alpes, UMR5168, F-38041 Grenoble, France CNRS, UMR5168, F-38054 Grenoble, France CEA, iRTSV, Laboratoire Physiologie Cellulaire et Végétale, F-38054 Grenoble, France INRA, F-38054 Grenoble, France.
Plant Gene Expression Center, USDA-ARS/University of California, Berkeley, 800 Buchanan Street, Albany, CA 94710, USA.
Ann Bot. 2014 Nov;114(7):1497-505. doi: 10.1093/aob/mcu185. Epub 2014 Oct 6.
The morphological variability of the flower in angiosperms, combined with its relatively simple structure, makes it an excellent model to study cell specification and the establishment of morphogenetic patterns. Flowers are the products of floral meristems, which are determinate structures that generate four different types of floral organs before terminating. The precise organization of the flower in whorls, each defined by the identity and number of organs it contains, is controlled by a multi-layered network involving numerous transcriptional regulators. In particular, the AGAMOUS (AG) MADS domain-containing transcription factor plays a major role in controlling floral determinacy in Arabidopsis thaliana in addition to specifying reproductive organ identity. This study aims to characterize the genetic interactions between the ULTRAPETALA1 (ULT1) and LEAFY (LFY) transcriptional regulators during flower morphogenesis, with a focus on AG regulation.
Genetic and molecular approaches were used to address the question of redundancy and reciprocal interdependency for the establishment of flower meristem initiation, identity and termination. In particular, the effects of loss of both ULT1 and LFY function were determined by analysing flower developmental phenotypes of double-mutant plants. The dependency of each factor on the other for activating developmental genes was also investigated in gain-of-function experiments.
The ULT1 and LFY pathways, while both activating AG expression in the centre of the flower meristem, functioned independently in floral meristem determinacy. Ectopic transcriptional activation by ULT1 of AG and AP3, another gene encoding a MADS domain-containing flower architect, did not depend on LFY function. Similarly, LFY did not require ULT1 function to ectopically determine floral fate.
The results indicate that the ULT1 and LFY pathways act separately in regulating identity and determinacy at the floral meristem. In particular, they independently induce AG expression in the centre of the flower to terminate meristem activity. A model is proposed whereby these independent contributions bring about a switch at the AG locus from an inactive to an active transcriptional state at the correct time and place during flower development.
被子植物花的形态多样性,加之其相对简单的结构,使其成为研究细胞特化和形态发生模式建立的理想模型。花是花分生组织的产物,花分生组织是一种有限结构,在终止生长前会产生四种不同类型的花器官。花按轮状精确组织,每一轮由其所包含器官的特征和数量定义,这受一个涉及众多转录调节因子的多层网络控制。特别是,含AGAMOUS(AG)MADS结构域的转录因子除了决定生殖器官特征外,在控制拟南芥花的确定性方面也起主要作用。本研究旨在表征花形态发生过程中ULTRAPETALA1(ULT1)和LEAFY(LFY)转录调节因子之间的遗传相互作用,重点是AG调控。
采用遗传和分子方法来解决花分生组织起始、特征和终止建立过程中的冗余性和相互依赖性问题。特别是,通过分析双突变体植物的花发育表型来确定ULT1和LFY功能丧失的影响。在功能获得实验中还研究了每个因子激活发育基因时对另一个因子的依赖性。
ULT1和LFY途径虽然都在花分生组织中心激活AG表达,但在花分生组织确定性方面独立发挥作用。ULT1对AG和AP3(另一个编码含MADS结构域的花结构构建基因)的异位转录激活不依赖于LFY功能。同样,LFY异位决定花命运也不需要ULT1功能。
结果表明ULT1和LFY途径在调节花分生组织的特征和确定性方面分别起作用。特别是,它们在花中心独立诱导AG表达以终止分生组织活性。提出了一个模型,即在花发育过程中的正确时间和地点,这些独立作用使AG位点从无活性转录状态转变为有活性转录状态。